Friday, February 12, 2010

Ulcerative Colitis Funny Sayings Steroids (prednisolone)?

Steroids (prednisolone)? - ulcerative colitis funny sayings

Hello I am 16 years old and was diagnosed with ulcerative colitis, when he was 14. When I was diagnosed with UC, I was put on medication terrible prednisolone 80 mg per day. I had terrible side effects moon face, cramps, etc. .. Anyway, during that time my life was hell for the people in my school who was my moon face funny place. Unfortunately, I had an outbreak and the doctor has me on 40 mg prednisolone. As you can imagine, I am very afraid to go to school, when I want. So I was wondering if it could help an idea or a thought that omitting certain foods like salt, that prevent the side effects and I also wonder if you could take a herbal remedy to the retention of Help "possiibly water . Thankyou for your help, I do not know what to do, I believe that my illness is ruinng my life and makes me depressed. I'm afraid to go to school.

10 comments:

happines... said...

Hello Princess - children of school age can soooo terrible - the most important thing is how he feels and to discuss these issues with a doctor - or better still, to beg him to a specialist hospital and advise headers only medical knowledge was limited. Please go as soon as possible - with the parents and find as much as poss. Search the Web for help. Good luck to you. Oh yes, and ask your parents inform the school about the behavior of their colleagues - the intimidation will not be tolerated, but the teachers must be aware of the situation.

tomimegi said...

Make contact your doctor, and if something else can be obtained. Other medications. Some doctors can help you go directly to other steroids treated as a last resort. I do not think you can avoid weight gain while on them.

In an attempt to limit the number of households in the UC, you can try Omega-3 - Fish oil has been studied at the University of California and know that actually contributes to reducing outbreaks. Pro antibiotics - Yogurt can also help to restore the good bacteria in the colon. Also try to eat up to 20 per day, blueberries do not know why they work, but noticed on the advice of someone who has Crohn's disease, and I ate, I make a difference very quickly. Even if you just avoid dairy products and the amount of red meat you eat.

Good luck to her trueFriends know what is new and I am sure that support them.

Inga said...

I need a Crohn specilist and gastroenteritis (reumatologist no!) And were in the same drug. Side effects may depend on the state of the body. One thing I have learned that the best way to defeat the aggressor and all the other crap that comes with a chronic disease, try not to take life, because then win both the UC and intimidation. Rounding out the short term view only look at your diet and lifestyle and which elements can be controlled to help UC, rather than focusing on the parts that you can not control. We wish him well and a speedy recovery. x

JennyJen... said...

Like you, I was diagnosed over 13 years. I have fun too bothered about other people and me about it. someone who actually started the rumor that the bees have something for the whole face might sound strange, but if people come to ask how it happened not so funny. I also have the confrontation with the moon face and other side effects. When he about 2 years I am surprised that you doctor is not recommended Remicade. I used drugs for too many, and I thought that the disease was taking over my life, but they know that only a problem in life that we do, unfortunately. since he began treatment with Remicade, you only take 14 tablets a day and every night an enema, but it's better than about 30 tablets a day with the face of the moon. Remicade is an infusion andme about 3 hours. I read every month and lasts until I return. I relapse, but to help enemas. Remicade is given when not in a position to reduce the prednisone for one year. I was recently on the treatment with Remicade and put wow! It helps. I also wonder to see if you have a family physician or a gastroenterologist? You must see a gastroenterologist, because they specialize in your state too. I would definitely ask your doctor to a specialist and Remicade to be seen. If you need information, please contact me. simply nice to know that someone who feels the same way. Your friends dont really understand what is happening and what can be a normal child. In any case, hope that you feel better!

browneye... said...

They put me on prednisone since 2001, when I received a kidney transplant. The moon face and weight gain is normal. What I found was that no matter what you eat, how they are still in the steroid, which will face the moon in the form and sent a crazy appetite. I've tried to make a supply of water, exercise, and diuretics. Nothing gained. But gradually I was outside and saw the weight of the voices in my body. But it was the stupidest thing what you ever did. Now I am being rejected: (

smk said...

Unfortunately, there is much you can do to prevent side effects of prednisone on. 80 mg is very high. Is I was diagnosed with UC, there are almost two years. I was up and down in mg mg of prednisone for about 1 1 / 2 years (at 40th) At any given time. What I can say is that I have taken several months before I face her "Moon" showed side effects. Perhaps their UC will have to be controlled after a short time on steroids and have not reached that point.

Ulcerative colitis is very difficult. If you have outbreaks, you can eat some fiber, low residue diet (you can find guidelines for yahoo.com). Diet to help control the outbreak of a little.

Your doctor should do everything possible to get steroids, because they are very bad for the long term. My dOctors take steroids, if I am and what was the answer to everything. Then I met my current doctor to help find alternative drugs to reduce prednisone. There are other drugs there as Imuran, Remicade, Rowasa and methotrexate. They all side effects of anxiety, but I have a great doctor who assured me that the very bad side effects are rare. If you do not get to work a different medicine for you, then you can get from steroids, which is an absolute necessity for this, what I have read and heard.

Do what you can help you eat food to heal your colon. This would be a start. Do as much as you can research. There are many opportunities out there and other useful information.

We hope that this information is helpful.

stef8705 said...

Ive had prednisolone for the treatment of asthma has bold me not to discuss violence, absolutely, and to find another medicine, an attitude, your health and your life, just say no to that, to me that you take things that I feel bad.

yellowba... said...

not for long. Maybe the doc could give on the fifth day pack of steroids to take place. You should see a rheumatologist, you may have Crohn's disease. There are better treatment for Crohn's disease.

More or less Cosmic said...

Contact your support www.nacc.org.uk

alec A said...

It's amazing how different people take this medication. If I prednisone asthma is out of control. I feel life I'm hungry until I eat something and then to give me bad indigestion constant nuisance for the duration of the medication. Sorry for the problems on the moon, the children can sometimes real Gits.

Post a Comment