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Hi everyone,
I am starting Humira as soon as my prior auth gets approved. Having a rough time these days. Diagnosed with ulcers extensively above my pouch last June 2012 which indicates Crohn's now. Also have been on prednisone for arthritis of IBS and Xifaxan for chronic pouchitis which was exacerbated over the past 6 months. I am hopeful that Humira will help everything. Anybody else out there dealing with this? I am weak daily but push myself because I refuse to give in. Have anemia but oral iron supplements not absorbed and I was hospitalized with anaphylaxsis last August after an iron infusion. Hoping the Humira will calm EVERYTHING down and I'll be able to absorb iron, have less or no more accidents, have no more pain, improve my pouch function, stop hurting from the arthritis and get off of prednisone. I'm not asking for too much Smiler Thanks for any input. Sorry for the vent. A little frustrated waiting for the insurance to approve.
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I don't have Crohn's, but was put on Humira for enteropathic arthritis back in 2005. Did not have complete relief of the arthritis, but I didn't need a cane anymore. My pouch improved greatly too. I now take Simponi (monthly injections), and am doing well.

I only take prednisone for very short periods for acute arthritis flares now, maybe once a year.

Jan Smiler
You can ask your doctor to change the Rx to the prefilled syringe. I think doctors just assume everyone would prefer the pen, but once you get over having to throw a dart at yourself, it is so much better to be able to control the speed of the injection,or even pause it until the intense stinging stops. The pharmacy will not switch it without an order, since it is specifically ordered that way.

Other tips to reduce the stinging (regardless of the type of syringe you use):

1. Let the syringe sit out for an hour, at least, before injection.

2. Ice the injection site for a few minutes before your injection.

3. Don't inject the thigh, the abdomen is better (less sensitive).

Jan Smiler

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