Prednisone Reviews


Prednisone (Prednisolone)

Prednisone (Prednisolone) is one of if not the most common medications that is prescribed for ulcerative colitis patients.  It is a synthetic drug, and is used to treat inflammation.  Prednisone is used to treat many other conditions besides ulcerative colitis.  Crohn’s Disease, asthma, tuberculosis, and thyroiditis are just a few on a very long list.

As with many medications, the side effects of Prednisone/Prednisolone can often be extreme and enough to make people literally hate the steroid.  Prednisone has been commercially available since 1955, which makes the data and known side effects relatively easy to learn about.

Search Side Effects Below:

CLICK HERE to add any side-effects you’ve experienced.

Other Meds
Central serous retinopathy - is an eye disease which causes visual impairment, often temporary, usually in one eye.[1][2] When the disorder is active it is characterized by leakage of fluid under the retina that has a propensity to accumulate under the central macula. This results in blurred or distorted vision (metamorphopsia). A blurred or gray spot in the central visual field is common when the retina is detached. Reduced visual acuity may persist after the fluid has disappeared = NOT FUN!
September 7, 2018
Extreme swelling , easily bruising
Tylenol 3
May 25, 2018
Shaking fever
April 27, 2018
weight gain,
moon face
March 12, 2018
Weak legs, atrial fibrillation, excess desire to eat, loss of concentration
March 4, 2018
Moon Face
Increase in hair growth on stomach
Increase in appetite
February 19, 2018
Feeling Agro
Had to take sleeping pill
Sulfasalazine for sure.
Rowasa? Not sure it was a long time ago... but have used it, it was difficult to use
February 6, 2018
Excessive acne
November 18, 2017
Made me crazy, hyperactive, gain weight. Got a stress fracture in my foot
from walking off the excess energy.
November 16, 2017
Oedema and skin rashes
August 2, 2017
lialda and loperamide
July 25, 2017
shortness of breath , anxiety , mood swings , insomnia .
July 11, 2017
Mesalamine enemas
Steroid enemas
July 2, 2017
Diabetes (type2), osteoporosis , beginning of cataracts, insomnia, shakiness, heartburn/acid reflux, palpitations, rapid heart beat
July 1, 2017
muscle pain
July 1, 2017
Sensitive teeth, weight gain, headache
Lialda, Effexor 75 mg
May 22, 2017
Moon face
Weight gain
Blurry vision
Sore throat
Skin tags
May 10, 2017
Shortness of breath
Vaginal mucas/blood
Pro biotic
April 18, 2017
Hair thinning.
December 19, 2016
Hair loss/thinning.
December 19, 2016
Sleeplessness, a bit hyper but it makes feel great. Tapering off right now, was up to 40mg a day for two weeks.
Lialda, Omeprazole
December 11, 2016
Serious spike in eye pressure related to Glaucoma.
November 13, 2016
Ah, where do I start. I just saw my doctor Monday who told me "you basically have all the aide effects you could have, to their extreme." Awesome.

-weight gain (I have what's called centripetal obesity)
-increased appetite
-muscle weakness
-lower back pain
-irregular menstrual cyclet
-facial hair growth (I now use facial nair for women)
-steroid induced bipolar
-crying all the time
-talking a lot
-extreme dry skin
-easily over stimulated in large or loud groups
-decrease in sex drive
-wounds heal less quickly

That's all I can think of for now!
Delzicol 400mg
October 23, 2016
Severe stretch marks all over my arms, back and thighs. Don't know how to get over it
Immuran, mesalazine.
October 23, 2016
Was prescribed 60 mg a day about four months ago. Most notable side affect was nervousness, shaky hands, weakness and tingling in my extremities. Also had anxiety, insomnia. Finally being weened off this med. I'm currently taking 15 mg a day now.
Azathioprine, Mesalamine
October 14, 2016
Sweating, specially night sweats, weight loss, hair changed textured but became nicer, hunger all the time, hard to sleep. Puts me in a great mood.
September 18, 2016
Face swelling up,mood change,bad side effects trying to get off ofprednisone
September 15, 2016
6th day after stopping uceris and starting prednisone....some stomach pains are back, diarrhea more than I had it on the 7th week of uceris.
Hungrier but could be in my head. Bloated pretty bad. No other side effects so far.
No other
September 15, 2016
Daily: Sweating, puffy skin, thirst, hungar, weight gain, adrenal rush, ringing ears, unclear decisions. LONG TERM: (3months doses, prescribed every 18months for Chrons flare ups; total usage after 7years, bone scan revealed significant bone loss!
Azathioprine, asacol then, pentasa, then colazol, then lialda
September 9, 2016
Insomnia, heart burn & reflux, leg weakness, feeling low, strangely weight loss, agitation, severe tiredness in the afternoons, palpitations
September 4, 2016
Moon face,weight gain,weakened bones(deficiency of calcium),Candida,mood swings,heart burn,mouth ulcer .etc
September 2, 2016
Acne, depression, bone pain
Entyvio, tacrolimus, dificid, citalopram
August 27, 2016
Leg weakness
Hair loss
Foggy head
August 24, 2016
August 16, 2016
Weight gain
August 15, 2016
Weight gain, insomnia, irritability, acne, hot flushes.
August 12, 2016
August 10, 2016
lack of sleep Acne Moon face
Asacol Azathioprine
August 9, 2016
Mood swings
Weight gain / always craving for food

August 8, 2016
I was able to finally taper off of prednisone for the first time in two years. I am currently experiencing severe joint and muscle pain in most of my body. So far my stomach has been good but these pains keep me up at night.
Entyvio Infusions
August 8, 2016
Acne, severe thirst, issues with my blood sugar really high around 10-15, couldn't stop eating, put on 35lbs in 4 months.
August 8, 2016
Muscle pain in quad directly above the knee in both legs, caused pain when bending and a constand dull ache.

Swollen ankles midday making it painful and difficult to walk.

Swollen left thumb.
August 8, 2016
August 7, 2016
Feeling dizzy when turning quickly. Nauseous when driving.
August 7, 2016
Massive weight gain
August 7, 2016
Moon face
Trunk fat gain
Insomnia (now chronic insomnia for the last 3 years in UC remission - not sure if triggered by pred or UC)
Hair loss upon tapering

Mesalazine (Mezavant)
August 7, 2016
Hair loss, 10 lb weight gain, overall feeling of bloating.
was not taking another med at the same time
August 6, 2016
Hair loss
Pentasa, imuran
August 6, 2016
Increased frequency and diarrhea. Severe insomnia, depression and anxiety.
August 5, 2016
Hair loss, weight gain, swollen body, swollen face, moon face, joint aches, increased appetite, increased heart rate
July 28, 2016
i got way bigger. unbearable joint pain that curled my spine and prevented me from walking. insatiable appetite. mood swings
July 28, 2016
gritty teeth, joint pain, gritty teeth, shutting down my emotions, anxiety, no energy at 3pm, awake at 3am, and my favorite - moonface
Lialda, which was insufficient to maintain remission

Today, 6 years later - no meds, in remission
July 28, 2016
Weight gain. Blurry vision.
July 27, 2016
Acne, moon face, weight gain, mood swings, insomnia, osteopenia.
Asocial, immuran
July 27, 2016
Heart hurts when breathing in
July 27, 2016
Severe heartburn @40mg
Staph infection @40mg
July 27, 2016
Severe mood swings, achiness, headaches
July 27, 2016
High blood pressure cannot sleep made feel strange no sleep had to go on a sleeping pill. Had to take water pill to bring down pressure ended up in hospital 3 days the water pill took made my sodium level go way below normal .....Abd the sad part was on Predisone 30 days did not do a thing for my UC....
July 27, 2016
While on a 60 mg (7 days for each 60 thru 10) Prednisone taper for 6 weeks, I experienced inability to sleep through the night; jitters; weakness in my legs; weakness in the muscles in my thighs. My legs felt very heavy and I found it hard to walk up stairs in my house. Around the 4th week of taking the Prednisone, I would need a cane to help support myself. This was the second time on the Prednisone. I was also on it last year for 6 weeks and in addition to the above side effects, I also developed a soreness in my right ankle and then it appeared swollen and tender to the touch. Went for an ultrasound and found out I had superficial phlebitis in that area. I don't know if it was directly related to the Prednisone, but I didn't have it prior to taking this medication. One good thing is that once done with the Prednisone, the strength comes back in the legs. I also took Vitamin D3 and Calcium while on the Prednisone, and also ate more bananas for Potassium.
I was also taking my diuretic for BP, and the second time on the Prednisone, I was started on Lialda for my UC.
July 27, 2016
Moon-face, insomnia, hunger, hyper, osteopenia and osteoporosis later on - 59 yrs. old now. Did nothing for my U/C symptoms and have not taken any since.
July 27, 2016
red spots weakness in lower legs
July 27, 2016
Hair loss after stopping prednisone
July 27, 2016
Every course of steroids gives me rosacea which is a flushed red face and spots (after food). You can get rid with oral antibiotics but this causes colitis to flare. You need to take the topical cream for 8 weeks to clear.
July 27, 2016
Leg pain thigh
July 27, 2016
Catteracs within 4 weeks of taking a high dose
July 27, 2016
Anxiety, depression, major mood swings
Lialda, Azathioprine
July 27, 2016
Weight gain, hair loss, acne, swollen face, thinning of skin, dry skin patches, fatigue, high heart rate , night sweats, insomnia, weakness
July 21, 2016
Moon face that lasted months, severe weight gain due to always being hungry, night sweats, mood swings and trouble sleeping
Salofalk granules 1.5mg
July 20, 2016
Weight gain, moon face, insomnia, easy to bruise, thin skin resulting in stretch marks, osteopenia and osteoporosis, hip fracture.
Asacol, colazol, uceris, Humira
July 20, 2016
Extreme night sweats, joint/ knee pain, tremors in my hands, insomnia, mood swings
July 20, 2016
Rapid heart rate, weight gain, trouble sleeping, chipmunk cheeks, acne, anxiety from knowing all the bad things that can happen with long term steroid use!
I've had to combine Prednisone with different meds. I am now combining them with Humira. In the past I have combined them with mesalamine. I've also combined them with Canasa. I've also combined them with sulfas. Doesn't matter what I combine them with, they still produce the same side-effects.
July 20, 2016
-Reduced sleep
-Dry skin on hands to the point of cracking
-Moon face
Lialda (started 1 month into Pred)
July 19, 2016
-sensitive teeth from anything slightly cold
-tongue sores and pain
-weight gain
-things smelled and tasted different....almost metallic
-severe hair loss
Remicade and Imuran
July 17, 2016
July 17, 2016
Extreme sensitivity to cold on my teeth. I had to drink everything through a straw it was so bad. When I asked my GI he said it wasn't the Prednisone but my dentist thought it could be. Now that I see other people have had this side effect, I know it's for real. Plus a few weeks after I finished the medication the sensitivity disappeared.
July 17, 2016
Weight gain
July 17, 2016
Extreme agitation, anxiety, headaches and red face at 40mg dose. Increased appetite.
July 17, 2016
Not able to sleep, pain in knees, alot of hunger, mood swings
July 17, 2016
Prednisone: insomnia at high doses, joint pain in fingers when weaning off.

Salofalk (mesalamine): no side effects so far.
July 17, 2016
Shortly after taking a high dose of prednisone, I began to feel sensitivity in my teeth, that only after inquiring with my dentist did I learn is something that many other patients have experienced.
At the time I was taking a 5-ASA medication called colazal
July 17, 2016

If you have taken prednisone/prednisolone and would like to submit your own review of your experience with the medication, please feel free to write your review here:

Prednisone Reviews:

Click here to submit your review.

Submit your review
* Required Field

Prednisone Prednisolone Prednisone is a steroid that is used to treat inflammation for ulcerative colitis patients. SKU UPC Model


Nov 27, 2016 by Nolan
City/country:: Tacoma USA 

If there was ever a movie about prednisone, it would be called The Almost Living Dead. Fortunately I don't remember too much about the 2 months I was on it. It should be called zombie in a pill. I still keep a few on my computer desk so every once in a while I can mutter a few old sailor oaths at it. I still have leaky gut but am just about in remission.


Jun 02, 2016 by Karie Huffine
City/country:: Karie 

Predisone is a horrible drug. Yeah sure there are ways to deal with symptoms and sometimes I give in and take one usually at 2 am. I hate the heat flashes more then anyrhing. Doesn't help my appetite any which really sucks. But I gotta say thank you to Judith Pausina "predisone worse then the disease" 2014. I've been reading through everyone's complaints and b4 that I read an email about genetics and uc. I have had an over active immune system my entire life could be genetics but everyone has the potential of it, or an under active immune system. However processed foods is a huge culprit. I also had an injury to my neck at birth which could also have a lot to do with it. But as I'm reading I'm wondering why isn't anyone saying anything about their immune system. they not realize this is a major cause of any form of IBD. Thank you Judith for saying it..stable your immune system get off all medications. I'm almost down fall though is nicotine (stimulant) and to much caffeine(stimulant). And another thing' stimulants not only irritate the bowls it activates the immune system along with stress.

Just try it

May 28, 2016 by Connie
City/country:: Pleasant Hill, CA 

Have had colitis for 26 years and avoided taking prednisone during my initial flare ups because I was afraid (from all the horror stories you read about). But please -- if you are suffering from IBD, you owe it to yourself to at least try it. Prednisone always works quickly -- within a day or 2 -- to calm down my flares. My bleeding stops within days, and I feel so much better. My doctor usually starts me at 40mg, tapering by 10mg every 2 weeks. Yes -- there are side effects. I am lucky in that I do not have too many negative effects. My husband tells me that I get "a little aggressive" and I do notice that I have snapped angrily at telemarketers on the phone or at bad customer service folks, which is not like me at all! I also get very hungry and tend to gain maybe 5-10 pounds, but there are ways to help control the weight gain. Cut out extra salt. No more Lay's potato chips! I try to eat lots of fresh fruit and veggies and even when I'm exhausted, I try to take short walks to keep my metabolism going. This really helps to control the hunger and bloat. You might get a bit of a moon face, but it goes away eventually, and I'd rather have moon face then the blood and pain. Please don't let bad reviews freak you out -- at least try it. It's not a long-term solution, but it sure helps me to get my life back on track.

First time's the charm, second time, not so much.

Mar 05, 2016 by Alexia
City/country:: Canada 

The first time I was on prednisone was after a flare up in 2014. At that time It was discovered that my colitis had progressed and I needed to start prednisone to get the flare up under control. I started a 8 week course at 40 mg and tapered down 5 mg per week. This worked very well for me and I stayed in remission for a year in a half. ( I am also on Salofalk 500 mg tablets 4000 mg per day and 1000mg suppository).

My second go around with prednisone has been less successful and I am currently having difficulty tapering off successfully without symptoms coming back. I started off at 40 mg and got down to 20 with occasional symptoms creeping back,by the time I was down to 10 mg I was in trouble again. I am back up to 15 mg and tapering down 2.5 mg every 3 weeks now. I've had occasional bleeding (1-2 per week).

In summary, I think prednisone is good at knocking down the symptoms quickly, but getting off of it can be difficult and my GI doctor has stated he doesn't want me to become dependent on steroids either.
I've been lucky in that I have had no severe side effects from the drug except sleeplessness when I was on 40-35 mg of prednisone.

Love/Hate Relationship

Feb 23, 2016 by Erika
City/country:: AUBURN 

I take 10mg of prednisone after each Remicade infusion for 10 days. It helps keep the joint pain down. Since it's a low dosage, I don't see many bad side effects as you get when its a higher dosage. I do get irritable during this 10 day period and anxiety. Sometimes I have trouble falling asleep but once I'm sleeping, I'm fine as long as I don't have to wake up to an alarm clock in the morning. I do have acne and back acne that I can't get rid of. The drug works very fast to relieve joint paint. I have also found I have a drug interaction with antibiotics and remicade. When this happened, all my back and neck muscles start freezing up and I turn into a cripple within a few hours. Once I take prednisone and go to sleep, I wake up like nothing was wrong the night before.

Feb 13, 2016 by Robert
City/country:: Vänersborg 

Would like to say that i am a scots guy living + working near gothenburg, Sweden, 57 years old and in nov 2015 had symtoms similar to uc.Gp sent me to gastro specialist for a coloscopy, went not so good because of severe inflamation.
So put me on predosoline, same as everybody else, l assume..50 mgs 3 days then 40 for a week untill now 13 feb 2016, am on 5 mgs every second day for my last week so what can i say so specalist called me last week to say it was not uc i have because of the results of my 2nd coloscopy biopsies on 11 jan 2016, he said it seems to be some other inflamation i have but they do not know what it is so i have to submit a stool sample for cal proctein level.
After i said that with predesoline it was fantastic but as i an now on 5 mgs the bleeding was back again he said to continue comming off the meds untill the course is finished ( next week ) and as he is now going on holiday for 2 weeks, if i have acute problems i must go to emergency dept...
Good luck to me then...anyway what i have felt with this drug is mostly in line with the the begining perfect how it stopped everything & back to normal for the first few weeks.From 50 to 40 ti 30 all was okey then 25 and 20 and 15 then the effects started.
Pain in my left forearm only, dizzy different periods of the day, shakes in fingers a little, sweating a lot AFTER passing a stool ( something that resembles one ) night sweats a little, nor a lot.The biggest effect i had was the next day after i had a little whisky or two, as i am scottish of course i like my weekly tipple but on this drug ( by the was says zilch on alcohol usage on my prescription advice & my doctor said nothing about intake of alcohol, maybe i was naive or an idiot) the day after was a massive hangover, i mean i thought i was dying, after only 15 cl of whisky this was not good.
I stopped drinking whisky 3 weeks ago & just had a beer ( one pint ) & 3 glasses of red wine.
That was not worse but heavens above so little alcohol & i felt like i consumed one litre of whisky.
So last night 2 glas white white wine, no beer no whisky and this morning went well in the toilet!! Ye ha i thought, looks good so far but alas after my tea its back again so we will continue to see how this weaning progress goes in the next week.
No great hopes but i am mostly mild in comparisson to a lot of people with real uc.
Maybe i will find out what i have soon..keep the hopes up everybody out there !!!

Nov 13, 2015 by Rachelle
City/country:: Old bridge 

About 13 yrs ago I was diagnosed with Polymyalgia Rheumatica. The treatment recommended was Prednisone. Starting on a high dose and quickly weaning down. I felt fantastic while on it, but unfortunately when they weaned me off, I couldn't move. So much pain.
I was finally told that I was misdiagnosed and when I did have was Poly OsteoArthritis. Last February I had my first flareup with UC. I never felt so sick in my whole life. The pain and the uncontrollable running was horrifying. I went to the doctor and he prescribed a colonoscopy. He told me that from what he sees, didn't warrant the pain I was having. He started me on different medications, but unfortunately nothing worked. Still being on prednisone he raised it to a very high dose then to wean off again. The side effects this time is horrible. I was raging, I couldn't sleep, I was gaining weight rapidly. I could not stop eating. Finally he weaned me down, and the pain and discomfort that goes along with the UC immediately came back. He then sent me for a sigmoidoscope, and then again told me that the pain and suffering I was going through didn't relate to the results of those tests. My rheumatologist told me was not unusual to have both arthritis and ulcerated colitis together. They agreed to put me on Humira. Unfortunately, I could not afford the copayment of $1000 a month. So, they decided to put me on Remicade, and I recently took my third dose of infusion. what I laugh about, is the fact that my insurance company is paying $26,000 a dose. They wouldn't cover the Humira . At this point I am still having stomach pains but the colitis is changed to now constipation, and my arthritis seems to be a little better. Needless to say I'm a little disappointed, because I am still on the steroids. I would like to know is why can I not take a higher dose of the steroids and get off the Remicade. I am told that the prednisone is much more harmful than the Remicade infusion. I am beside myself, since I have felt that there is like nothing that is really working. I am giving the Remicade another dose,and make my decision from there. In the meantime I am weaning off the prednisone again and I'm down to 5 mg a day. What I suggest to anybody taking prednisone, to not stop it suddenly. I did that one time and I was the severely ill So now the doctor told me to wean off as slowly as I can. If anyone has any suggestions, I would so appreciate it. I feel like I am sick every day. I feel like I am running a few errands and exhausted, but no fever. I'm wondering if this is a side effect of the Remicade.
Thank you for letting me vent.

Only as a last resort

Nov 13, 2015 by Lauren
City/country:: Seattle 

I was put on Prednisone as a last result since my flare was so extreme. They couldn't even finish my colonoscopy as the disease had caused my colon to become so inflamed. I took a very high dose and then started tapering after 3 months. The side effects are absolutely horrible. I didn't sleep the entire time I was on the medicine. I constantly had to urinate. I got moonface. The medicine cause me to be "mean" as my family would say. It also caused my hormones to be all over the place for over a year. Only almost 2 years later, do I feel like my hormones are finally balanced. This is a medicine that I never have to go on again, although I know that it is required by most insurance companies in order to take other medication like Remicade.

Not so bad

Oct 12, 2015 by Hendrik
City/country:: South Africa 

I see a lot of negative reviews of Prednisone, but I have found it to be semi effective. I am still new to the UC scene, only diagnosed in August 2015 with a very mild flare up. So far I have not experienced the extreme conditions that some people seem to suffer. But in the short 3 months that I have been living with UC I have had two flare ups. First entocord suppressed it and then Prednisone. I am now going through my third flare up, again a mild one, while I am on Prednisone. I was supposed to take the Prednisone for 5 weeks, slowly waning off of it, but after three weeks I had another flare up. BUT it was not because the Prednisone did not work. Apparantly I also have a viral infection in my colon that is causing the flare up. I did not gain weight while on the Prednisone, in fact I lost 2kg instead!, and I did not get any mood swings or had any other side effects. So for people who have mild UC flare ups like I do please do not fear Prednisone as not all of us suffer from the side effects.


Aug 30, 2015 by Sen
City/country:: Ireland 

I was diagnosed with UC and I was put on this medication after a colonoscopy. It didn't work properly for me as it took so long to build up in my system. I eventually had to be put on remicade as my disease worsened. They side effects are dreadful!! Mood swings and weight gain not to mention multiple more side effects....


Aug 29, 2015 by David Opon
City/country:: Homer Glen 

I have had Uc since 1982. The first few years were tough, but the went 20+ years without much problem until March 2014 since then two flare ups and prednisone (40mg...30mg...20mg weaning). First flare up irritability big time. This time a (20mg...10mg...5 mg 15 day boost; followed by the monthly 40 mg...30mg etc.) I am irritable (but not quite as bad) but have insomnia and noticed my hair thinning. I'm 58 yea r old male, so could be unrelated, but didn't notice it until I was weaning off the 15 day boost. Heard Biotin might be helpful to counter hair thinning/loss? Anyone have input?

Prednisone for UC Ruining Marriage

Aug 28, 2015 by Cindy
City/country:: St. Louis 

My new husband on prednisone and has turned into someone else. It is just awful. I had no idea...

Works but with a catch

Apr 29, 2015 by Ashley
City/country:: London 

Prednisone does work wonders for UC but I would rather be I'll than go on this medicine again. The side effects are horrible for me; night sweats, mood swings, water retention, weight gain that is almost impossible to get off. There are much better options than being stuck on prednisone, at least for me personally.

It's a funny one

Mar 06, 2015 by Richard
City/country:: Guildford 

Yep, I concur with much I have read in these reviews. Suffered badly with U.C. for 6 or 7 years, wouldn't touch steroids, heard bad things about them. About 8 years ago I tried them due to feet swelling up double size. Worked instantly, virtually no side effects except for a feeling of extreme well-being! Nowadays I go on 40mg one day, 35mg, then 30, 25 etc i.e. an 8 day course. Works mostly, but these days it really messes with my head. I'm also on Ibuprofen most of the time. Having said that I'm on the SCD at the moment and many U.C. symptons gone but this diet is really messing with my head!!! Overall it's been very positive in helping me live a normal life.

Horrible stuff for long time use

Sep 02, 2014 by SHARON
City/country:: Silver Spring, MD USA 

I have mainly been on prednisone for lupus for 48 years, so I can only review for that. I spent 10 years on 100 mg a day! I felt as if I was dying as everything was such an effort. For short term use, yes, do it. For long term, try not to. I gained 400 lbs, had to have my knees replaced 3 times (always check your knees as it eats the bone), and have permanent problems due to it. In 1996, I quit going to my doctor, who said I couldn't live without that much, and took myself down off of it. I now take it only for short bursts. YES, I know I wouldn't be alive now without it, but I feel much better without taking it constantly. I did lose 250 lbs, and am doing well, but at 19, it was too much. DO NOT STOP IT SUDDENLY- be sure a doctor takes you down as yes, you could die- I had been on it so long that I knew what I was doing taking myself down. When first taking it, you only want to sit in front of the open refrig door and eat. Yes, yearly eye tests, mainly by a retina specialist, is part of it. Moon face will always be there due to taking it for so long. If you are on it for a long time, remember your body makes prednisone on its own, and when you are on it, most of joint pain goes away; but when you come down, your body isn't making it naturally, so you have withdrawl at first (quite a bit of pain), and then it will level out as your body starts producing it again. I totally recommend it for short time or low dose only. Hope this helps, Sharon in Silver Spring, MD USA


Sep 01, 2014 by Hannah
City/country:: Maidstone, united kingdom 

Prednisone is a love/hate drug for me. Its been the most effective medication I have tried so far, literally making me fully better within just 2 days. However at times I feel I would rather be ill than have to deal with the side effects such as the horrific mood swings and difficulty sleeping as well as the swollen (moon) face and unbelieveable weight gain (1.5 stone) in just 2 weeks!! If there were a medication which worked just as well as prednisone but without the side effects then it would be the perfect drug.

Sep 01, 2014 by Lisa

I gave this medication a 4 because it worked pretty fast in getting my flare under control....& when i say fast, i mean FAST!...within 24 hrs. I heard all kinds of horror stories abt side effects...luckily i experienced minimal. The only side effects i encountered after almost 6 months on pred (started at 40mgs and then weaned), were excessive sweating & very sensitive to cold teeth. Thats it! I know the long term side effects of this med are bad so i dont know if i'd wanna go on it again unless i HAD to (would like to try Endocort or Uceris), but if i had to i would cause it did work quite well.

Sep 01, 2014 by Kristen

In the past, prednisone has worked wonders to get my flares under control. I didn't have any weight gain or moon face, but I had some swollen ankles and knees. Also, the Pred didn't work on my last flare, but this could be because I came up positive for cdiff. I do have osteoporosis now and prednisone might have been a contributing factor to this. I worry a lot about the long term side effects more than the immediate ones. I'd give Pred 5 stars if it didn't have such terrible side effects.

Sep 01, 2014 by Kristen
City/country:: Columbus 

Prednisone did help get me back in remission, but the side effects were almost worse than my flare. Extreme roid rage, body acne, hungry ALL the time, not sleeping for weeks, bruises that make it look like someone is beating me, indigestion, etc.

looked like I ate thanksgiving dinner alone

Sep 01, 2014 by Lindsay
City/country:: Canada 

I was on prednisone for 6 months. At a high dose for 3 of those months before tapering. I am grateful it helped put me into remission as a 65 day flare led me to the hospital.....and doctors panicking over how sick I was. first no one told me you shouldn't take it at dinner. For the first few weeks I was a ball of energy at night. I cooked my way through the Canadian living magazine (for 4 months!). Over time I became rounder; very self conscious; exhausted; struggled with my moods; had prednisone muscle tremors all the time; heart palpitations that required potassium pills; could drive; forgot EVERYTHING!; wanted to eat everything!; and eventually by thanksgiving last year, it looked as if I ate the entire dinner alone. The hardest part was coming off of it. The withdrawal made me very sick. My poor family had to watch me struggle on and off this drug----and with "crazy me".----so glad im back to normal now! While it helped save my life, it doesn't come without a price.

Sep 01, 2014 by Jenny
City/country:: Canada 

Hello. I was on this drug for 13 weeks back when I was first diagnosed in 2011. At the time I it really helped with getting me on the right track to putting me on remission. But now as I am learning more about it I wish I would have been given more options from my doctor.
This Friday I am on the way to have a glaucoma test because because my eye doctor believes Might have it which is pretty common of people using presldnisone.
When I was on it made me hungry. I ate all the time. Made me sleepy. But at the time I didn't have all the information about it and like many people I just wants to feel better. I had a one year old at the time.
I just wish I was more educated. So my review would be use at our risk but educate yourself first! It's serious stuff and needs to be stressed that by doctors.


Aug 31, 2014 by KIM LUGLI

Hi to all you Prednisone users,as a retired Pharmacist(due to LUPUS) and on Prednisone for 20 years here are a few tips for coping with Prednisone,always take before bathing or showering if not your BP will increase,always take with or after food,keep hydrated carry bottle of water or non acidic juice,do not take in the evenings otherwise you will be hanging from the chandeliers or dancing around the room at 3.00 a.m in the morning.Never take with alcohol and NEVER stop taking your daily
prescribed dosage without consulting with your DR or you could go into Cardiac Arrest.Also you should be on a diuretic LASIX or Puresis which is the generic and you should also be taking doses of Potassium as Prednisone does deplete the body of Potassium causing Low BP
- Slow K or the generic PLENISH ask your Doctor.You will quite often get horrible bruising as your skin does become very fragile but you can use REPARIL GEL which is actually a muscle reliever,but is great for bruising,a fact not well known,but I have used with great success,as at times I can on my hands look like
I have been in a fist fight and many people remark about it,if there is anything else
I can think of to help you cope will do another review,hope this assists Regards Kim
Johannesburg South Africa

Prednisone not always bad

Aug 30, 2014 by Aaron 35
City/country:: Toronto/Canada 

Was on prednisone for 6 months from 50 mg down to 35 back up to 50mg now 0 :). Want people to know that it isn't always as bad as what you read. I was really scared to be on it bc of what others went through, but in my own experience the side effects were worth the outcome so remember that. After a few months my face puffed up slightly but not a lot, my acne increased but knew it was temporary, and my hair thinned a bit and would fall out daily but totally manageable. Compared to what I expected to happen wasn't as bad so if ur just starting it don't worry, not everyone gets terrible side effects and a good chance they will be manageable bc they are only temporary.

watch side effects

Jun 08, 2014 by Todd

I was going thru a bad UC flare - 9 months. I have UC for 10 years and really am a mild case. They gave me prednisone for 3 months. It helped with the flare up, but I gain about 30 lbs, my face became rounded and I had a very short temper. Now spring 2014 going thru another flare up...worse one so far and was on ulceris for 1 week. did not help. GI doc put me on prednisone again and flare up/bleeding much better. Now on reducing dosage for the next 4 weeks and noticing other side effects: night sweats, hands jittery about hour after I take the meds, and increasing pain feet/legs cramps. This last one is really the one that is bad, especially at night. I know of the other signs from before, so I watch how i speak to others.

Jun 01, 2014 by Dawn

Predisone works fast (40mg) to get rid of a bad flare up but then it takes forever to wean off. The side effects are facial hair, moon face, always feeling hungry, weight gain.

Predisone worse than the disease

Apr 04, 2014 by Judith Pauisna

I was given predinisone when I was 20 yrs old and first diagnosed with Crohns. I tried to take it for about 6 weeks. The side effects of terrible acid indigestion, hair growth on my face , weight gain, my face and body bloated and disfigured. I threw it away. I felt it was worse than the disease. I continued to be sick and had a couple of surgeries until I walked away from the doctors. My hope for anyone with Crohns is to read about others who have improved their condition using meds for help with symptoms( diarrhea, nausea, pain, fever, etc); but the real answer lies in learning to help your own immune system work. This means high fiber diet of cooked fruit, vegetables, rice, chicken/fish and no harsh grains. I started by resting my intestines by drinking Spirutein meal replacement as a smoothy all day long. Whne I felt like I could eat I did. This was all I did forabout a week or two. Then I added Vitamins. They were Zinc, Vitamin C, Magnesium, Calcium, and Vegan Omega #3. I did this for a long time and in baby steps. While doing this I read as much as I could understand about inflammation in the body, about auto immune diseases, and about vitamins and what each one can do in your body. That is it. Not complicated but consistent and never giving up hope. I found hope in reading about other people and how they were doing something very similar and succeeding. There are thousands of us out here who have overcome Crohns in this matter. Please consider this: you must care enough about yourself to start to make choises that are the least stressful in evry phase of your life. Crohns is not caused by stress but it is exacerbated by stress. If you have personal, financial, or other problems you must seek a stress free solution . You will get better. It has been proven. Please consider that you are the someone who can overcome this debilitating misery without the strong meds . My best wishes and stronger yet, my prayers for each one reading this is that you will accept my recommendations. SPIRUTEIN see through google, I still live on it every day and it keeps me strong.

Trashed my bones

Sep 15, 2013 by Tristan

Prednisone failed for me. I was on it for 6 months and it never did anything.

When Remicade + 6PM + Lialda ended up working, I was taken off prednisone and met with a specialist who did a bone density check. He told me that the prednisone had hurt my bone density so much that I had the density of a 70 years old (I was 39 at the time). It took 2 years of calcium supplements and lots of dairy to built things back up.

So this one's not for me.

Only thing that has worked for me, and had no side effects

Sep 14, 2013 by W.

I have had U.C. for 7 years and have been through all the different types of mesalamine, sulfalazine, and some I've forgot the names of. 2 years ago I had a flare up that was mild but would not go away. I was in flare until about 4 months ago when I started prednisone and mesalamine suppositories. My flare went into remission until I got down to 10mg of prednisone and no more suppository (all while stil taking my lialda). about 2 months ago I was prescribed sulfalazine...didn't work. now i'm on prednisone and about to start purinethol. I have not had any side effects at all from prednisone, yet my dr. said its not a long term fix so he's switching me to the purinethol.

The one drug I will take

Aug 23, 2013 by Don Makowski

Prednisone works so well for me and the side effects don't really bother me at all. I need 60mg/day for it to be effective during a flare but I notice immediate relief from diarrhea, mucus, urgency and bleeding. I don't sleep very well on it but I have learned from this sickness to be able to relax and meditate in bed and get as much rest as possible even though I am not sleeping. My joint pain disappears and my muscle and tendon tightness disappears. It's a miracle drug for me and I am so happy to feel a little bit normal again when I take it. I do notice some irritability and have to do a lot of apologizing to my wife. She is very understanding and that helps. I know that when I have tapered in the past my symptoms have come back. I think it was because I tapered too quickly after getting down to 5mg/day. Last time I lowered the dosage by 1mg per week until I was off and I was fine.

Never Again

Aug 22, 2013 by Katie

I was diagnosed with UC almost 3 years ago. I have been hospitalized twice and am currently on the 6MP. Of the 3 years I have had UC, I have been on prednisone about 2.5 years of that. this last flare up was bad and after being on iv steroids in the hospital I went home still on the prednisone.. it was the worst experience with side effects I had ever had. irrational thinking, scared, paranoid, suicidal, sever weight gain, couldn't walk due to pain in my knees, night sweats, missed periods, angry and sad all the time, back pain, blurred vision, bloated face and stomach,weak.. I finally went in and they put me on what they considered a VERY FAST taper. I had them put in my file, I will never again be on prednisone. If that results in surgery then so be it but I wont go thru this again. I am currently in remission for now. I know for me stress is a huge factor so I just try to keep things mellow and take my medicine. I realize that choosing not to ever be on prednisone again will limit me if I have a flare up but I just know for my sanity I cant do it. I have 3 kids and it really altered who I was too much. Very scary. I remember when I first got sick I thought prednisone was as wonder drug cause it helped me and my side effects were minimal but now, it doesn't even help unless I have the IV and then im still stuck on the pills.. 40mg. Glad to be off it now. Evil drug!!

Prendisone - ugh!

Jul 29, 2013 by Jennifer

I was diagnosed with Ulcerative Colitis when I was 29 - I am 40 now. It is in my family - dad, sister, aunt, and cousin are all afflicted. The first time I was diagnosed, the gastro prescribed Asacol, which made my symptoms so much worse that I ended up in the hospital for about a week! In the hospital, I was given prednisone intravenously and then took it orally after I was released. Had some weight gain (mainly in my back), increased acne on face and body, moon face, very emotional, increased hunger.....but did make flare go away.

I stayed in remission for many years, but just began experiencing more frequent flares about two years ago. Each time I have taken prednisone and had the same side effects. However, this time I am also experiencing numbness in my arms and legs (mainly my left side), which is really scaring me. I am going to see the gastro tomorrow to discuss these new effects. Also, I just started spotting and it is not time for my menstrual cycle, which is definitely not typical for me. I have been very emotional - crying uncontrollably. I am also anemic, which has caused much weakness. I am currently on 40 mg. per day - been on this amount for 10 days. Still experiencing diarrhea, but less frequently than before - still blood. Hope to taper down to 30 mg. at the end of the week. Just really worried about the numbness in my arms and legs - it is really scaring me. It feels like there has been muscle loss. Also, my toes are getting purple - seems like a lack of circulations. Scary!

Jul 28, 2013 by Linda

Was on Buderisone for a few weeks when my flare-ups came back. Dr. put me on 50MG(5 pills) to start for two weeks and then 4 for three weeks and so on and so on. Also was on Hydrocortisone Rectal Suspension. After the first week my flare-ups went away. By the second week the puffiness started appearing. By week 4 my face look like a puffin fish. The back of my neck was so tight I could on lift my neck up a little. My ankles and legs were so swollen that my husband said I had cankles. I had put on about 30pds. I know it wasn't all fluid, but being on predisone you could eat anything and I always felt hungry. I have been off predisone for three weeks and I have only lost about 3lbs, and I am hardly eating right now because of gallbladder problems.
Hope to never have to take predisone again.

Prednisone Side Effects: Much better than UC symptoms

Jul 06, 2013 by Haley

I have been on Prednisone (along with Asacol) for 2 weeks and I noticed immediate relief from my UC symptoms. After the first 4 days of being on the steroid (before starting the Asacol) I had no more stomach pain, bowel movements eventually returned to normal (no more blood, consistency was normal, bowel movements weren't frequent)... Basically, I felt back to normal for the most part.
After a few more days (after adding the Asacol dosage), I started feeling sore around my neck, upper back, and around my underarms. These areas were sensitive to the touch, but it would only last for a day and it doesn't happen every day (so far, only happened twice). As I understand, these are areas where lymph nodes are located. Seeing as Prednisone suppresses the immune system in order to get rid of the inflammation, it makes sense to me why these areas would be sore from time to time.
I've started getting acne on a small area on my chest and more on my face. Steroids can mess with your hormones though, so this I also understand.
I have an increased appetite, but after the months of being in pain after every meal and losing a significant amount of weight from the anxiety of said stomach pains... I'm very glad that I can eat whatever I want without being in pain and I'm happy to gain back the healthy weight that I've lost!

So far, the side effects haven't seemed very troublesome to me. I'd take these side effects over the UC flare up any day! Just looking on the bright side.

Balding and Barren

Jun 24, 2013 by Jessica

I was on Prednisone for 2.5 months. I did not gain weight, although I did get a bit of a moon face. Prednisone messed with my ovulation cycle and now, after tapering off and being steroid free for 3 weeks, I have started losing my hair! I will NEVER take prednisone again. It didn't help anyway; I had to go on Remicade soon after starting due to severity of symptoms.

Jun 22, 2013 by RobR

I was in the middle of a bad flare due to my own negligence and stubborness. My doctor prescribed prednisone and took it without even looking up the side effects. It really helped and didn't suffer any noticeable sides. I consider myself lucky especially after reading some of the comments below. I was on a 10 day taper so perhaps I wasn't on it long enough but after 3 days I actually experienced two regular bowels, in a row even ! Because of this turn around I have now set my sights on a low carb high prorein diet.


Jun 08, 2013 by meghan

Prednisone ... I was started on 40mg and was amazed, i had alot of joint pain and within a day i felt great. My appatite sky rocketed, as for sleep i always had trouble sleeping anyway so that wasn't any different. I am noe on 25 mg and it'a starting to wear off, my joints are getting a bit sore as off the last week. So i'm thinking this is just short term which i suspected anyway.


May 02, 2013 by Josh

I was put on 40mg taper while my flare up was out of control. I literally ran to the bathroom 3 time in the waiting room for my doctor. The Preds made me very short tempered. Stupid stuff would aggravate me. After about a week I would still get mad but I would take a few breathes think about how stupid the things that were bothering were & I was good. The other issue I had was loss of sleep from 40-20mg I had allot of sleepless nights or just a few hours of sleep. I didn't gain any weight. I actually got a few comments about losing weight when I was on it. BUT THE BOTTOM LINE IS THE PREDS WORKED! I noticed results by week 2. My 20-30 trips to my second office reduced drastically to 5-10! By week 3 I had no more blood & was going to the bathroom only maybe 3 times a day. For me this was night & day! Ive now been off Prednisone for a month & have not bleed since the first week on. My stomach is still holding food from time to time & Im not going normal every time Im going but as far as the bleeding & constant running to the bathroom Im good.

Prednisone sucks

Apr 26, 2013 by Karen

SO back in March I was put on Prednisone for the very first time. For me it helped somewhat with the inflammation and my frequent bathroom trips. I started at 40mg a day for the first week. The first few days on it weren't bad at all. I even lost about 3 lbs. I thought wow so far so good. After several weeks on it the weight gained started. My face and neck swelled up. I have now gained 13 lbs total since starting. I feel like crap with the extra weight on me. I have been tapering down and as I taper down the side effects get worse. I had some weeks of horrific night sweats. Now that I am on 15mg a day I do notice I don't get the night sweats. I am constantly hungry and crave carbs all day long. If I start craving a food I need to eat and if I don't I get very nasty. I did in the beginning go through major mood swings and depression. I am finally out of that just wish I can start losing weight but I do feel like I am retaining water and feel a bit bloated plus I know I had a huge increase in calorie intake.

However it has helped quite a bit with my UC flare up. My symptoms are slowly but surely improving and I just wish the bleeding would stop but my GI doctor said it will come with time.

I don't care what kind of flare up I have again but never ever will I take prednisone again. I am so looking forward to the day I am off it!

Weight Gain!

Apr 17, 2013 by Reina

I was prescribed the drug in December of 2012.. it was working wonderfully I was not having any blood any accidents nothing till I realized how fat a was getting from the face! ..I gained almost 2O lbs of water weight & immediatly told my GI doctor to get me off. The drug does its job itS wonderfull but with awfull side affects. Now iam on imuran one pill a day. And I feel good exsept with all that extra weight on me

Tough drug but did it's job

Apr 11, 2013 by Caroline

I was put on a 40mg taper to try to get out of my first UC flare. I generally try to do things more naturally but things had gotten pretty dire - within a couple of weeks, my 20-25 daily episodes of bloody d reduced to 5-6, with no blood. I continued to improve throughout the 2 months - I have also been doing the Paleo Autoimmune diet as well, plus probiotics, glutamine, vit d, and fish oil. However, I needed the prednisone to jump start things for me. As far as side effects go, I did not have the typical ones of weight gain, mood swings, and insomnia. I was actually more tired than usual and had no trouble sleeping - however, I did have significant muscle wasting, loose ligaments in my ankles, and numbness in my calves. Thankfully those side effects went away once I was completely weaned! Hopefully I never have to take it again but I am thankful it helped me when I needed it.


Apr 07, 2013 by Skip

I was put on 60mg of pred. &375mg of apriso I've tapered down to 5 mg of pred hoping the Apriso( mesalamine) would keep me from flaring up. Unfortunately today ( my last day on the pred ) my symptoms came rushing back. My doc said to go back up to 40mg which I did and almost immediately I stopped running to the bathroom every 20 min. I hate the side affects but I hate the UC symptoms worse. I just read Adams books and will definitely be using he's cook book after I ween down from the pred. Hopefully I can become medicine free myself it's worth a try ! Right now I'm in Taiwan visiting my daughter& family so it's tuff eating right ,but as much as I can I am using Adams cook book!

stay away from this

Apr 01, 2013 by moe

Well, It helps for the short term but it comes at cost.. I almost had all the side effect it caused me a lot of teeth problems

well worh it

Apr 01, 2013 by Dean

diagnosed with uc 1984.tend to have couple of flares a year on average and have had 2 two week holidays at good hope hospital over the years,coming very close to the knife on both occasions. i use prednisolone when i flare up and decide my usual meds are not going to bring it under control.i always find they have an almost instant effect and the side effects are a small price to pay.I start with 30 mg and up to 40 if need be,but i start down dosing when i feel i am back in control.My usual meds are asacol,mercaptopurine .

Did Not Work For Long

Mar 28, 2013 by Jennifer

Diagnosed 1983 with UC. Oral Prednisone has never accomplished anything for me except exacerbation of symptoms except for while in hospital.Accupuncture worked for me for years, then finanaly didn't.Was on Asacol/Mesasal for 28 years with recurring flare ups and was still prescribed prednisone (which did not do anything except make symptoms worse). Tried every treatment that was reasonable (medication, diet, lifesthyle changes, exercises, etc) which did not work. Finally had and ileostomy in May 2012. AFter 29 years the old intestine had finaly given up the ghost.The surgeons could not believe that I had not had surgery at all before that, but guess what? I have NO PAIN. If you have to have surgery you have to have it, and it is a lot better than being chronically sick.

Necessary Evil

Mar 25, 2013 by Andy

Prednisone helped me with my first flare up and I was on it a relatively short amount of time. It is a wonderdrug for inflamation of any kind but if you stay on it for very long and/or in high doses, it eventually becomes worse than the ailment you took it for. I had a flare up of my UC last year and was on as high a dose as 80mg for several months and it just wouldn't work like it did the first time. My face swole up into a moon face. My back, chest and arms broke out in the mose unsightly, painful acne you could imagine. I went to a new gastro and he put me on Imunran but I had just started a cycle of pred tapering from 40mg so I needed to taper slowly and be done with it. I did so until about 3 weeks left on my taper when I got sick and decided if my body was going to heal, I needed to stop taking one of the immunosuppresors I was on so I dropped the pred with 3 weeks left on my taper...folks, I almost died from that. I was a very healthy competitive Brazilian Jiu Jitsu player and if it wouldn't have been for that, I probably would have died. It's been about 6 months since I've been on prednisone. My back, chest and arms are clear of the acne but dark scars remain, hopefully they'll go away with a little sun this summer. Imuran is working wonders and I pray I never have to see another prednisone pill as long as I live.

It worked for me

Mar 24, 2013 by StormCat

I was first put on Pred last September when my first round of meds stopped working completely... I had lost 0ver 10% of my body weight in a month and my Doc was just trying to get everything to stop for a minute so we could determine where to go to next... He started me on 80 MGs (I'm a big girl as well, so that was probably part of the larger dose)... Well it worked for me immediately... After a month he started dropping it down by 15 MGs every 3 weeks until I was off completely... The only side affect I ever really felt was at the very beginning... For those 2 weeks, I could have eaten the papers on my desk, if I'd thought they were halfway tasty... I stocked myself with as many healthy snacks as I could because it seemed like all I wanted to do was eat!! But other than that, I didn't seem to have any other side affects...

Mar 24, 2013 by Bethany

I was first put on Prednisone in October of 2012 when I was first diagnosed. I started at 40mg and for about a week when I was in the hospital the second time at 60mg. I am now, 5 months later, finally down to 10mg and tapering at 5mg a week while going on to Humira. As much as the side effects of prednisone suck, I would definitely take it again. It brought me out of the woods and actually made me feel like me again. Granted it took a month and a half to work but I was also very sick. The moon face and joint pain is child's play compared to full blown flare symptoms.

can not get of Prednisolone

Mar 23, 2013 by anne

Hi there I had a sever flare of my colitis in 2011 I was put on initially Hydrocortisone infusions 1000 mls 4 x a day for 2 weeks thank then put on 40mg prednisolone but sadly each time try and droped the dose I would get worsening of symptoms. so my GI suggested dropping 1mg a week I finally went down to 5mg and have been on this dose since but I still have 5-10 times bowel movements or more a day. I have had to recently up my dose again back to 15mg as I started having watery diareah again and feeling quite unwell again, my new gi has me on a new regiment of medications and is hoping that the new dose will hope settle things down until the new meds kick in. hate the side affects and it caused me to get diabetes, when I increase the dose above 10mg I start getting side affects again I suffer from moon face, become moody and irratible, increased hunger, sweating uncontrolably and start getting knee and leg pain. Love the drug but hate it at the same time. I would love to come of it if I could


Mar 22, 2013 by Gerald

Hi there I have had colitis since I was 17 and now im the start of the disease I was on prenisone for a long time 8 pills a day..40mg a day for a couple years. but now I starting to have some bone loss (ostiopedia) that my doctor believes its becasue of the prednisone... I would never take it again and also the moon face really sucked bigtime.


Mar 22, 2013 by BUST-A-MOVE

While the long term effects is a concern for me, prednisone has been a life saver. Diagnosed in 2009, I've taken the drug for 6 month each of 2010 and 2011. I seem to get a flare at the beginning of winter and it takes until the end of April to get my immune system working effectively. I've never gained weight using this drug. It has given me so much energy I guess I just run off the calories. The last episode I noticed the moon shape face but, not before that. I also appreciate that all my muscle aches and pains go away. It really is an amazing drug. I plan on continueing useing it if I need to. (This winter I left the cold and stayed healthy-surprise surprise). I am mid fifties, active woman.

Prednisone...helps me!

Mar 22, 2013 by Rosanne Robinson

Over most of the past 30 years I have taken prednisone. It has pulled me out of the woods many times. I have had bone density tests over the years and knock on wood I am still good. I look at it as quality of life. I know there are risks...but I need to have a quality of life. Right now I am on 10 mg for the past 6 months...down from 50. I would pick to be on it if necessary.

Last Resort

Mar 22, 2013 by Allison

Unlike most, I suffer constipation and had a terrible 6 month flare that wouldn't quit. I nervously tried prednisone (50mg) for the first time after Jan 2013 colonoscopy confirmed that the UC was very active. So, now that I am on my last week (yay) I can review in hindsight.
Let's see... it was wonderful to have no systemic inflammation (forgot what that felt like) and having 2-3 normal BMs with no pain everyday. And although I barely slept the first 6 weeks, I was so happy to have energy and feel good that I may have opted to try to stay up 20 hours a day. Hah!
The dark side was the prednisone rage I would sometimes feel. Yikes! my hair falling out in clumps, chubby little face, joint pain & the uncontrollable hunger. I needed to put on 20 lbs so in the end it all worked out.
I feel the inflammation creeping back a little but I have renewed hope that remission is around the corner. Keeping my diet very strict & carrying on with food intolerance testing in 3 weeks. :)
I hope to never take prednisone again... I worry about the liver damage & osteoporosis etc., but it is always there as a last resort.
Good Luck to everyone.

Better than being sick

Mar 22, 2013 by Trisha Collins

I have had UC for 13 years, first 2 were misdiagnosed as IBS. I only have to take this when I have a reoccurance and at first the side effects were horrible with the high dosage. However, I learned to take it very early in the a.m. as so not to become sleep deprived. The other side effects I learned to deal with and it is the ONLY thing that can get me back to living a fairly normal life. As my outbreaks have become fewer (thanks to natural probiotics, aloe juice and dietary changes) I have found that I rarely need it and when I do it works quickly. I have tried other meds but this works, plain and simple. Also, it is affordable compared tot he alternatives!

Good, but hate the side effects

Mar 22, 2013 by Chad

I have used prednisone on two different occasions over the 11 years I have been diagnosed with UC. The first time I took it for about 2 months and things weren't so bad. The side effects were minimal, but the UC was being treated and I was having normal bowel movements after a couple of weeks of taking the medication. About year 8 I went through a bad spell with UC and ended up on prednisone for about 6 months and the side effects were real bad. I put on 20 pounds, 175 - 195. I had the puffy face to go along with the weight gain, sore joints and always hungry. I went off of it and swore never to go on it again. The good thing that came out of this was me keeping track of my diet and what bothered me and what didn't. I think that is HUGE in the battle of UC. You need to know these things so you can control at as best as possible yourself. I am currently taking 4 Lialda a day and weigh 170 pounds and exercise regularly to keep my stress level down which also causes flare ups for me.

Great Results

Mar 22, 2013 by Graham

I was diagnosed in Nov 2012 and Prednisone saved me. I was in incredible pain and hadn't had a solid movement for over 2 months. I was feeling better after a couple weeks of Pred and became less reliant as i tapered the doses down. I agree there are some side effects. I was irritable and always hungry but it sure beat being irritable because of the pain and not being able to eat solids for weeks. I am a believer in this medication for short periods of time. It is the sole reason i felt better and was able to enjoy Christmas with family.

Mar 22, 2013 by Rachel

I was on 40 mg. It worked when I was on the high dose, but when I went down to about 20 mg I started getting symptoms back again. And I absolutely HATE the side effects! The moon face was horrible! It went down after I was off of it, but it never completely went away!

Not too bad

Mar 22, 2013 by Therese

I was diagnosed with Colitis Jan/2012. After the enemas/Lialda did not work, my doc put me on 40 mg of Prednisone. It worked very fast and I tapered off for a few months. I had minor side-effects; a little weight gain, a slightly swollen face, and felt jittery (like I drank too much caffeine at the higher end of the dose). It worked pretty fast and got me out of my flare. I transitioned to Lialda and have not had another flare.

Good and Bad

Mar 22, 2013 by Zach Tatro

Prednisone is probably the only drug that I know for sure has helped my since I was diagnosed in March 2012. Unfortunately since then I've only been able to get completely off of it once and that was only for a few weeks before I had a flare up again. Currently I'm back down to 10mg per day, about to go down to 5mg's tomorrow. I implemented a diet change 2 months ago which seems to be helping me out. I'm hoping that weaning down from 5mg's to 0mg's very slowly this time around, along with my new diet will allow me to stay off predinisone longer this time. At high doses(I was at 60mgs at one point) I definitely had the night sweats, moodiness, some moonface, and of course crazy hunger. I've had joint pain but I'm not sure if that's just from the colitis or a side effect of the meds. Overall I just don't like the feeling of being dependent on a drug that you know is hurting you in the long run(weaking of bones, ect). For me at least though taking prednisone still feels like a better option than having surgery.

Good and Bad

Mar 22, 2013 by Zach Tatro

Prednisone is probably the only drug that I know for sure has helped my since I was diagnosed in March 2012. Unfortunately since then I've only been able to get completely off of it once and that was only for a few weeks before I had a flare up again. Currently I'm back down to 10mg per day, about to go down to 5mg's tomorrow. I implemented a diet change 2 months ago which seems to be helping me out. I'm hoping that weaning down from 5mg's to 0mg's very slowly this time around, along with my new diet will allow me to stay off predinisone longer this time. At high doses(I was at 60mgs at one point) I definitely had the night sweats, moodiness, some moonface, and of course crazy hunger. I've had joint pain but I'm not sure if that's just from the colitis or a side effect of the meds. Overall I just don't like the feeling of being dependent on a drug that you know is hurting you in the long run(weaking of bones, ect). For me at least though taking prednisone still feels like a better option than having surgery.

Not worth the side effects

Mar 22, 2013 by Lisa

Prednisone slowed down the frequency of bm's, but did nothing for the consistency or blood. I blew up like a balloon, couldn't sleep, got night sweats, and lost a bunch of hair.

Mar 22, 2013 by Jennifer

I love Prednisone for my colitis. It works within a day or two. I have energy, my bms decrease from 15 to 5 in a couple weeks, and the cramping goes down significantly. It is a miracle in pill form. And now for the side effects. All of the usual ones, moon face, hair growth (esp on my back as a lady), irritability, feels like I am on crack, and psychosis. I already have bipolar and because of the mixture of Prednisone six years ago, I attempted suicide. Annnnnd despite all of those side effects, I will always use Prednisone.

A great tool, but heavy on the side effects

Mar 22, 2013 by Shana

I've been on Prednisone several times and I learned that if its done right its a wonderful drug. For me (130lbs and 5'6ish) I loose all symptoms in


Mar 22, 2013 by Erin

While prednisone is a great drug for feeling better quickly, I HATE IT!! I was on high doses for a long time when I was in high school. Let's just say that teen hormones, stress and prednisone are not a good mix. I was a monster! I wanted to fight everyone, tried to hurt myself, was so aggressive. I am 5'2", so I wouldn't seem threatening, but I as on a 'roid rage'.
I ate like a line-backer and was thankfully so active that weight wasn't an issue, but my face was so moony...I felt I looked disgusting. I have sweet 16 pics that I don't want to look at because of it! Plus I had people, including teachers make fun of me. Being called 'cabbage patch' by a teacher was pretty low.
Plus the headaches, major headaches. And sleeplessness. I don't know how I made it through! Ugh. I felt like I imagine mania to be like; I hated it!
And now that I have been on pred many times and for so long, I have to worry about my bones. I am at high risk for osteoporosis anyway (short, white, normal weight woman) so I have more to worry about. I actually go for a dexa scan on Monday.

I would NEVER go on pred again unless it was the only option. It is a great drug in an emergency, but otherwise, I refuse.

Love Hate Relationship

Mar 22, 2013 by Chicago Jake

Worked GREAT at eliminating my symptoms, but that's the only good thing I can say about it. On the negative side, it made me gain 20 pounds (still working on losing those four months later), it killed my tastebuds, and it gave me anxiety. And worse yet, the symptoms all came back two weeks after I stopped the prednisone. Now I'm Imuran (an anti-rejection drug) which also relieves UC symptoms, but with far fewer side effects.

One thing I haven't seen mentioned here: I'm on coumadin for a mechanical heart valve, an Prednisone way boosted my INR. I had to cut my coumadin dose by a third to get it back where it belongs. My doctor wasn't even aware of this fact and didn't warn me, but fortunately my cardiologist's staff was on top of it. Imuran, by the way, drops the INR so now I have to boost my coumadin intake! It's always something!

severe allergy

Mar 21, 2013 by Jennifer Scholefield

i was prescribed prednisone recently and was taking 40mg a day, after 3 days i ended up in the hospital with breathing issues, numbness and dizziness through out my body and severe panic attack. it may of slightly made my colon feel better but the side effects far outweighed that. i also had severe depression and blurred vision, i couldnt stop crying and i couldnt seem to keep my eyes open, the doctor at the hospital said i was allergic

Prednisone Turned Me Into Dragon Lady

Mar 18, 2013 by Katie Lovesy

I was diagnosed with Ulcerative Colitis in November of 2012. I have been on Prednisone and am currently finsihing up my last two weeks on this drug. It made me gain weight, my cheeks got chubby, and I experienced pain all over my body. But the worst part was how it affected my mood. I became easily irritated and felt like I was always on edge. I didn't want to be around others because of how negative I had become and I got very depressed on this medication. Next time I experience a flare, I will ask for something else. This was a terrible last few months. It seems to have worked as far as my colitis symptoms, but the mood change was just too awful for me to go through again.

My Relationship with Prednisolone

Mar 16, 2013 by Hayley

I was taking 40mg of prednisolone tapering down by 1 tablet every 2 weeks, and instantly I noticed that I could not sleep at night and was constantly exhausted during the day, my appetite increased immediately but I did wasn't gaining weight, in fact I was losing it. It wasn't until 6 weeks into using the drug that I noticed the moonface appear (I HATE IT)! As I tapered down onto the final dose of 1 pill I noticed the increased sweating start to take hold of me along with the increased hair growth. I have now been Prednisolone free for 2 weeks and sill sweating, still feel hairy and still have the moonface. I did not get the mood swings at all, I was very emotional in the begining therefore was prescribed antidepressants that put a stop to that. Would I take Prednisolone again? Yes if it was the only thing that was going to make my colitis symptoms subside, it worked wonders for me.

HATE, HATE, HATE Prednisone

Mar 15, 2013 by Rebecca Aye

I HATED prednisone. I became very, very emotional and could not stop thinking about food--all the time. The strain on my marriage was intense--my marraige survived, but just barely. It took months and months to get off of it, because I kept having withdrawal attacks. I gained LOTS of weight. There is absolutely NO WAY I will take prednisone in the future.

Mar 09, 2013 by Ashlee

I have been on Prednisone since November 2012. While it did help take care of some of my worst UC symptoms, it definitely came with some side effects, too. I got the night sweats, insomnia, slight moon face, acne, and tooth sensitivity. All of my hair from the waist down stopped growing, but from the waist up it got darker and thicker (including my upper lip...and I'm a girl, haha). Shortly after a meal my BP shoots up for a bit, too. I started on 40 mg/d and have tapered down to 20, but past that my symptoms get way worse. I loved this drug at first because of the increased energy and symptom control, but I can tell my body is ready to be rid of it, as am I.

Mar 09, 2013 by anne

I have been on hydrocortison and/or prednisolone since being in hospital in october 2011 I was put on 1000mg 4 x a day of hydrocortison after being rushed into hospital with a severe flaw of pan ulcerative colitis. I hate the stuff and my emotions were all over the place one minute I was crying next angry and moody couldn't sleep put on weight. sadly I have not gotten of them since 2011 but know I am on either 10mg or 5mg doses prednisolone. I wish I could get of them but I think it is the thing that helps my UC. on new medicstions now trying MTX, pred, flaygyl and rifaximin and another medication Rifabutin which I am waiting to pick up

Mar 07, 2013 by Bev

Terrible side effects while on it: anxiousness was the worst one, but was angry and sad too. Horrible withdrawal side effects when I discontinued...severe nausea was the main one, extreme fatigue, skin crawling, felt like I was dying.
I hope I will never HAVE to take this drug again. I won't unless I am going to DIE.

Pred and my experiences

Mar 07, 2013 by Heather

I was diagnosed in June 2011 with UC. Went to May Clinic in Rochester, MN in Nov 2012 for 2nd opinion and UC was confirmed. I was considered by Mayo to have a mild case of Left Sided UC. I also had very low iron creating chronic anemia. Mayo Clinic released me back to my local doctor where I received Venofer via IV. I received 5 timed treatments of this liquid iron sucrose to replenish what my body had lost. Binding capacity put me out around 3 to 4 months to restore iron levels to a minimum. But that was only if I were to stop bleeding. I continued to bleed somewhere in the ball park of a few teaspoons to a 1/4 cup. I could not figure out how to control the bleeding. I had taken every pill known for UC including mesalamine and pred. It wasn't until I read about topical treatments on google that I started thinking differently. Topical vs taking pills was not the easier option. Topical basically means enema. I had had a very hard time understanding how that worked. I mean I literally could not physically keep the enema in. It made no sense to me. Then I read you're supposed to lie down after an enema. This made it easier. I started with Rowasa, 4g of mesalamine delivered topically. This was much better than the pills. But sadly they did nothing. I did Rowasa for 2 months and there was no change in my symptoms. I put it away and tried the SCD diet. I was good sticking to the rules for the first month but felt so deprived. Happy Hour sucked big time. Beer and pizza?! Forget it! So back to enema mesalamine, Rowasa, I went but this time my doc paired it with proctofoam HC. This is Pred but a topical version. What does that mean? -- fewer nasty side effects!

After 3 days of enema mesalamine and proctofoam HC, my BM's went from 8+ to 2! Zero blood after 3rd day. Less stinky after 1 week. Formed BM's after 2 weeks. Less stomach noise after 2 weeks. I'm now working on kicking anemia. Can't wait!

I made sure i did each enema treatment together - meaning Rowasa and Pred together. I would do this enema treatment 3 times daily -- if I had a BM and lost the meds I would reapply them to make sure I got 3 good doses in per day). This is the combination that worked for me with very very little side effects! I hope it helps someone else get better.


Mar 07, 2013 by Joanna

It was the only thing that cleared the flare ups up. Would start on 30mg and over 10 wks ween off them only to flare up a couple of weeks later, so the cycle continued for a couple of years in that pattern. On the higher doses I would be incredibly forgetful and fatigued, suffered pain in my joints and became bad tempered. On the lower doses I still had memory issues but energy levels were amazing. I fortunately, never gained any weight, actually lost some, didn't loose or gain appetite or suffered from facial bloating. So great in some respects but felt very out of control of my body.

Mar 07, 2013 by Kimberly

It worked wonders when I had a bad flare, within days I went from 20 bowel movements to 5 and then to almost normal. I have had to take it 3 times, all for about 2-3 months. The third time I took it it did not work well, I barely notice a difference, so I had the side effects but no relief. For that reason I will not take it again.
My side effects were that I was starving all the time, I would gain about 10-20 pounds, my face would get swollen and fat, I would be up in the middle of the night unable to sleep, I had a ton of energy despite lack of sleep. What I hated most was the change in my face, I felt so ugly.

evil prednisone

Mar 07, 2013 by gillian

i was on prednisone for about 9 months. it didn't help me at all but gave me all the aweful side effects. I blew up like a blimp, couldn't sleep, was super moody (understatement), could not remember anything seconds later, couldn't focus my eyes or attention, and was just plain miserable. that stuff can do so much bad stuff, my bone density also went to hell and every time i had to get an iv put it, it was so hard and would blow out in a day or less, made my veins horrible to work with. the stuff is just horrible. all good in small doses for limited time but long term it's evil.

devil drug!!!

Mar 07, 2013 by Lauren Snodgrass

When my doctor told me this medicine would help with the colitis pain i agreed to take it. I was on prednisone for 8 months 40 ml. i started at 125 lbs. at the end of the 8 months i weighed 164 lbs. and being a girl it caused a lot of problems. I went through depression, i hated being fat, the medicine itself worked in the beg. but about 5 months in i started geting all the pain back, bleeding and feeling like crap my doctor had me change my diet and added another medicine to my already long list to avoid starting me on remicade. At the 8 month point i told my doctor that he better take me off this medicine because i was turning into a crazy person, i had gained weight really bad, my moods changed (normally friendly to mean and really low patience) and the depression got really bad. He took me off and a month later i started Remicade and i must say its the best decision i've done. I call it the devil drug because it is!!!!

I HATE prednisone!

Mar 07, 2013 by ShannonRN

Everyone talks about how prednisone hypes them up? Yeah not me...I get depressed, weepy, dang near despondent, and I'm never hungry on it. In fact, I lost 15 pounds on my month long course of it! Never mind it took a good two solid weeks for it to do anything for me!
Luckily, my doc put me on entocort this time, which is helping marginally but I don't have as bad side effects on it.


Mar 07, 2013 by Sharon

I have a love/hate relationship with prednisone. I hate the side affect, i.e. increased appetite, weight gain, moon face, hair falling out, sweating, bruising, slow wound healing, but it sure does clear up my flares.

the worst possible drug

Mar 07, 2013 by joanna schupp

Prednisone is easily the worst drug I've ever taken (could be tied with Humira). I started on 40 mg a day and immediately gained 40 lbs of water weight. I couldn't walk, bathe myself, lift myself from the bed, brush my hair. My limbs were just so heavy. This caused permanent neuropathy and restless leg syndrome in my feet/legs due to the lack of blood flow and constant numbness. It's probably irreversible since I've been off prednisone for about 1.5 years now. I also developed night sweats, costochondritis (chest cartilage inflammation), anxiety, anger freakouts, shakiness, and severe insomnia. I don't remember sleeping for more than 30 minutes at a time and when I did wake up, I'd have to change my clothes and sheets because they were soaking wet. I learned to wear little clothing/no clothing most of the time so I wasn't constantly changing. I ended up living downstairs for the 3.5 months time I was on prednisone because I wasn't able to walk up the stairs. I used a walker to get from the couch to the bathroom.

I will never take this drug again. My doctors were just so emphatic that it would help my UC. It didn't do anything for that either, so the time I was on it was a total waste.

Worked the first few times

Mar 07, 2013 by John

I myself had some great success with Prednisone the first few times I needed to use it to stop a flare up. Side effects were mainly insomnia and increased acne, but it was still worth it.

2.8 5.0 80 80 If there was ever a movie about prednisone, it would be called The Almost Living Dead. Fortunately I don't remember too much about the 2 months I was on it. It should be called zom Prednisone Prednisolone

15 Responses to Prednisone Reviews

  1. Allison March 25, 2013 at 12:08 am #

    I LOATHE prednisone. I refused to go on it when I was first diagnosed back in 2006. I had an absolutely horrible flare in 2011 which forced me to go on it. While it stopped the flare, it completely disfigured me. I had dubbed myself the Prednisone Monster. I lost half of my hair (but that wasn’t from the drug but because I was so sick for so long. It’s your body’s natural response. I didn’t think so at first, but it happened again when I wasn’t on Prednisone), had a ginormous moon face, acne covered my body, including my face, mood swings, night sweats, an insatiable appetite, blurred vision, I was aggressive, couldn’t sleep, gained weight in areas I don’t normally gain weight AND I’ve developed osteopenia. Prednisone is a horrible, horrible drug. I’ll have to be on my deathbed (again) in order for me to take it.

  2. TiiniTete
    Tiinity March 25, 2013 at 6:49 am #

    No real benefit for me. My flares have never been controlled by the prednisolone and still I have been on high doses twice.

    Moon face and put on a lot of water, constantly in a high (good in the morning bad in the evening), hungry…

  3. Fitsum
    fitsum June 17, 2013 at 7:29 am #

    i have been in different doses of pred. it worked for me perfectly, and put me in a remission for quit a long period of time. minimizing z dosage whenever i felt good has helped m in reducing the side effects.i will take it for long as i should.

  4. uc familyboy June 24, 2013 at 1:08 pm #

    works but hits me hard with moonface and attacking my bones. recently been told I have osteoporosis. I dont think it is an option in the future for me anymore.

  5. don June 30, 2013 at 3:13 pm #

    I am 65 have left sided colitis since I was 30 years old.Handled most flares with diet and supplements plus enemas.I was never on any long term medication.Feb of 2013 I started bleeding and let it go for five weeks started to have abdomen pain went to er was admitted with white blood cell count of 18000 they put me of IV flagell and cipro for five days then I met a GI at the hospital he did a colonoscopy he said it looked like hamburger meat released me from hospital put me on 40 mg of pred for two weeks plus pentasa then dropped to 30mg for a week and then 20 for a week the flares kept coming so he put me back to 40 for two weeks he dropped pentasa and put me on Asacol. I had alot of pain when I tried to go to bathroom he did a rectal exam said he may have missed something did another colonoscopy the next day he said things look alot worse said I had to go back to hospital suggested Cleveland Clinic Weston Fla. he said there was a good surgeon there. I went there put me on 60 pred IV for 3 days released me started bleeding next day.Cleveland Clinic wanted to put me on Remicade but I had a slightly high tb marker so they wanted to get me down on pred and then retest for the tb.I am currently tapering down from the pred currently at 10 not really sure how to proceed from here my family doctor said drop to 7.5 and then call him and he will suggest what to do next depending how I feel.This is the first time for being on pred I hope its the last as far as side effects I really haven’t had to many other than legs and ankle sore felt really depleted on higher doses.After coming home from hospital read about scd diet on this web site started following it about a week into diet stopped bleeding and have not started back it has been about 6 weeks still using enemas usually one a day new GI wanted me on imuran to have something to fall back on if the pred flares I’m trying to go without it hope it doesen’t backfire.Want to thank Adam for this informative web site it is really helpful.

    • Adam
      Adam June 30, 2013 at 4:11 pm #


      Thanks for your update, and let us know what your GI says in terms of moving forward and getting off the pred. You’re super welcomed for all the info on the site, I’m glad you’ve enjoyed and made use of some of the pages here and hope to see you making some comments on how things go for you in the coming days months and decades.

      Best of luck and best of good health to you and you fam,

  6. Fitsum
    fitsum August 2, 2013 at 9:42 am #

    i am experiencing a very bad joint pain. i have been on it for more than three years. it is terrible. the worst part is that i am taking it ‘cos other medications are not available in my home country. may God help us

  7. Mack December 17, 2013 at 11:53 pm #

    I been taking prednisone for about 7 days 10mg I’m supposed to take it for 2 weeks then taper for 4 weeks I work out everyday and eat like a trainer small meals every 2 hrs will I gain weight? ???

  8. Caroline March 26, 2015 at 2:52 am #

    Hi all,

    Just wondering if anyone’s UC has burgeoned out into any other more serious auntoimmune diseases? I got a call from my gastro today saying he was concerned with my LFT numbers and that he wants me to start on Prednisone…. I’m really frightened of this drug. My UC has been fluctuating from proctitis to (once) further into the colon – UC – and I’ve been managed really well on pentasa granules morning and night and a morning pentasa enema. No bleeding, under control. My ANA count was 1280 – through the roof 8 months ago but no other symptoms suggested anything sinister so we were waiting to be guided by changes. I now feel DOG TIRED all day and night long and had rationalised that as switching careers in January. It could be rheumatoid arthritis, autoimmune hepatitis, Lupus – all sorts of real nasties. I don’t see him for a week and have also booked to see a functional medicine practitioner to get the low-down on alternatives. I am very worried. This is a frightening and lonely time. Has anyone else had a similar journey as me?

    Caroline. Diagnosed proctitis 2008

  9. cathy January 10, 2016 at 12:51 am #

    Beware because there could be no signs leading upto it after several months from complrting tapering off of prednisone my father took his life. He had no financial problems a loving and supportive wife and things in his life were more then fine he wasexcitef about winning and going to car shows. All he said was that he hated the way prednisone made him feel and he didnt like the person he became when he was on it. I miss him and wish he never started taking that prednisone the after tapering effects it had can never be undone. And the love of his life will always wonder why she didnt see it coming. So if tapering off after 5years of using please keep a very close eye on feelings and know it will pass
    Dont act on impulse

  10. James February 4, 2016 at 5:07 pm #

    Hi guys,
    I have been recently diagnosed ulcerative colitis with mild active chronic inflammation with ulcers in the colon, i am currently on prednisone 30 mg tapering it every week by 5 mg, 2 tablets of pentasa 500mg x 3, Colifoam enema once at night, probiotics and fasigyn. My symptoms have improved after starting the medication as i only have 2 – 3 bowel movements a day without blood but the problem is i have a foul smelling rectal discharge which is of great concern and it doesn’t appear to go away.I am extremely distressed because of it.
    Kindly share any solutions to get rid of mucus.

    • Adam
      Adam February 4, 2016 at 10:37 pm #

      I would recommend you get tested by your GI doctor for C-difficile. Your GI doctor will know what to do, it is tested via a stool sample.

      When C-diff is active, it often smells very bad.

      • James February 5, 2016 at 12:23 am #

        Thanks for you reply Adam, I have not been tested for c diff yet but the GI had given me a course of antibiotics twice for 10 days but it didn’t work out then he started these medicines. I don’t have diarrhea any more last time it was 2 month back but the problem of mucus is horrific

  11. Chris June 22, 2016 at 7:40 am #

    Nasty friggin’ drug!!!

  12. Richard August 7, 2016 at 1:52 pm #

    I just to wanted to re-visit a comment I made previously (Mar 06, 2015 by Richard
    City/country:: Guildford). Firstly, avoid Ibuprofen like the plague. I used the liquid form for years, as it was the only thing that gave me relief from the chronic joint pain I suffered, but I constantly flared up every few weeks. On stopping it (I now use celecoxib for the odd bit of joint pain I get) I had the longest ever period of remission it about 16/17 years and have far fewer flare ups now, and these are normally triggered by binge drinking (yes I know, but I’m just being honest). So for me, and I know everyone is different I have achieved a really good equilibrium by taking 10mg Pred, Mesalazine x 6, Calcium supplement, Chlorella Spirulina, & a 50 billion strain probiotic. Feel normal, normal stools, no blood, no mucus, very little joint pain. Not brave enough yet to drop to 5mg Pred, but will try soon………
    Two more points of interest I hope:
    1. I had my first ever colonoscopy at the beginning of the year (was a coward because I had convinced myself that there was a real likelihood of perforation) and I was diagnosed by the doctor who carried out the survey as having Crohn’s when it was originally thought I had Ulcerative Colitis. My consultant then wrote that I had Pancolitis. When I quizzed my GP about this on my last ever appointment with him, he said that it was all one and the same thing anyway!
    2. I cannot underline this point enough. For me the biggest by far player in my IBD is stress. Absolutely no doubt about this. No stress, no symptons.

Leave a Reply

This site uses Akismet to reduce spam. Learn how your comment data is processed.