Hemochromatosis Support Group
Hemochromatosis is a hereditary disease characterized by improper processing by the body of dietary iron which causes iron to accumulate in a number of body tissues, eventually causing organ dysfunction. It is the main iron overload disorder. Hemochromatosis is notorious for having symptoms that are often initially misattributed to other diseases.
Someone else had asked about hand pain, I had said I read somewhere that Arthritis is one of the things that do not improve with HH treatment, but I couldn't remember where I had read that. Since reading your post I went looking for it again.
"Treatment cannot cure the conditions associated with established hemochromatosis, but it will help most of them improve. The main exception is arthritis, which does not improve even after excess iron is removed."
http://digestive.niddk.nih.gov/ddiseases/pubs/hemochromatosis/
I had lots of complaints in the beginning, major ones being my hand and finger pain, stomach pain and fatigue. I was de-ironed in Jan of this year. I still have terrible hand and finger pain...
Oh well,,better than having all of the complaints. I will deal with it..I'm just happy to be diagnosed, treated and de-ironed. Even with the hand pain...I feel the best I have in many years!!
Things will get better, just hang in there.
Oh yeah..and I was one of the people who had bad experiences with my Phlebs, I could not handle once a week, I went twice a week, and for at least 3-4 days I was exhausted and dizzy! My Phlebs don't do that to me anymore.
Good Luck,
Patty
Funny you ask. That's what I thought I had when I was diagnosed with HH. I have read somewhere that tiny crystals form in the joints with HH and it's a sort of pseudo gout.
The joint pain sucks. It never got better, but let me tell you that I feel 1000 times better since being deironed. It wasn't immediate, but about 2-4 months after being deironed I was feeling MUCH BETTER!
"I could not handle once a week, I went twice a week"
I meant every two weeks..lol
With the WONDERFUL information and support I have found in this group, I think I'd reconsider trying the Wellbutrin, too. Ask the Dr if you could wait a little while to see if you feel better. Before I started phlebing.. I walked from the couch to the kitchen to my bed. That was my normal routine. THEN, I started feeling better after my 4th or 5th phleb.... weeks later I had some tiredness and felt like I needed a nap.
My ferritin has spiked up but other than needing a nap... I feel GREAT!
Last week I felt so good (while in Las Vegas) that I walked the "Miracle Mile" and MORE! and that was after my 13th phleb!! (Just 3 months after starting phlebs)
Good luck and give it a little time... you're gonna feel better :)