Humira, anyone?

Hi Everyone!

First time posting on this forum, but have been reading quite a bit for the last year every now and then when my hubby has a flare.  My husband was dx'd with UC in March 2006, everything seems to bother him diet wise.  However I am not with him 24 hours a day, so what I see him eat is very little and usually pretty healthy at night when we get home from work.  Within the last few months I was dx'd w/Lyme disease and put on a no refined sugar and very low carb diet.  Since I have been cooking this way for dinner or on the weekends, it seems my hubby has been in a small flare and then this last week a full blown very painful flare.   He stopped taking his flagyl and asacol about 4 months ago because it was causing him shortness of breath and low back pain (per hubby's dx) and 'not helping any ways'. :o(

A friend of mine at work has Crohns and has been using Humira and he said that it can be used for people with UC as well.  He can't say enough good about the Humira and he has had Crohns for 30 years and says tried everything to help (including the flagyl and asacol) him and nothing did until he got on the Humira. 

Finally my question... Does anyone here take Humira with a UC dx?  If so, is it helping you, have you had any side effects of it? 

One other question.. Do any of you take anything for the fatigue that comes with this?  My hubby could sleep for 24 hours if he didn't have to work and if he's not sleeping, he's very lethargic and has no energy to do anything. 

Sorry for all the questions... Thanks for listening..

I am not that well versed about Humira from a personal point of view. My Godchild's very good friend has suffered with a very acute case of UC for a number of years. She is probably 30 with several small children. Surgery was imminent and Humira was prescribed as a last resort after not responding to many other medications prior to that. This gal suffered very badly - don't know how she raised babies like many here on this forum - has a husband with a very demanding high profile job so she is home alone alot raising the children. He is a wonderful husband, father and provider but can't be there much to help her burden.

She is doing amazingly well and the surgery topic is off limits - or at least for now. She definitely has UC and not Chrons from what I am told.

hi

actually-i came to this website looking for humira info...my MD has recently suggested it for my UC, as the 'regular' routes are not working (ie/ been on asacol, now on 150mg of imuran)...and i wanted another option than prednisone (again)...apparently, they are doing some studies to see how humira works w/ UC pts...so i think i might join the study and try it out.

i know remicade is another option- but one good thing about humira is that its an injectable vs. infusion...not a big diff, but i have a small baby at home, and popping in to get a needle is better than having to sit and get infused.

 

My doctor said I might be going on it. Won't find out until the 6th.

Check with your prescription drug insurance company about direct-mail Humira - mine would charge about $400 a month if I got it at CVS, but going from the drug company directly, I have a $1000 per year max out-of-pocket cost, which would save thousands. The only problem is Humira has to be kept at a specific cold temperature, so they mail it with ice packs and it risks getting damaged in shipment. However, I think it'd be worth it to save a few thousand dollars.

Remicade is an FDA approved treatment for UC..... so you will probably see better coverage by your insurance company for Remicade. Your insurance company has the right to refuse to pay for humira because it is off-label for UC (some people also have AS or RA so they can get Humira for that instead of UC).... you can appeal their decision. Some insurance companies will pay for Humira for UC; I guess the way they look at it is that it is cheaper for Humira than a hospital stay. Right now it is only FDA approved for Crohns but some GIs will write scripts for off-label humira treatments for UC patients.

--Keith