Hello. My names Ryland and I was diagnosed with ITP in April. Since then I've been reading the articles on this website and the links that have been provided on this website. Since this is my first post here I'll summarize my ITP journey thus-far, before addressing the topic. (If you're solely interested in the topic I bolded the section where I address it.)
I ended up in emergency after experiencing horrifying nose bleeds for a long time. By the time I did anything about the symptoms I was covered in petechia and bruises. Lips, nose, arms, chest, just everywhere. The platelet count I started this whole experience with was a 10. I was given IVIG. Spent a week in hospital. Sent home without treatment. A week went by. My count dropped. I was prescribed Prednisone 75mg. Two weeks went by in which I learn that I'm basically disabled on Prednisone.
In may my appendix ruptures. I spend a week and a half in hospital due to concerns with the appendix site. It took me a week to start eating again. On the day that I'm released my Hematologist tells me that because of the complications I'm back to square one on the Prednisone Plan. So basically I was on 75 mg of Prednisone for six weeks. and then I was tapered slowly, by 5mg until I reached 50 and then 10 until finished.
The prednisone had maintained my counts at 110 except when I had surgery for my appendix. This is the second week I've been off of the drug. But I continued to read and hear of mixed experiences with prednisone induced remission. My hematologist had a patient who had remitted for less than a week, and another who had 10 years.
I guess Prednisone hit me harder than others? Since I have no idea how others could work on it. If I went for a walk one day then every muscle in my legs would cramp for the next two days. I drank so much gatorade to try to alleviate this. And the mental side was unbearable, I'd become unreasonably upset so easily. So I needed to find something to calm me down. Because after being on Prednisone for so long I was frightened I'd lose all of 2012 to ITP. And if I relapse the only initial option available to me is either IVIG/Prednisone or IVIG/Prednisone/Splenectomy through my current Hematologist.
So I went to see a naturopath. And he did some tests. And he prescribed copper and informed me I was a Histadeliac. I'm putting a lot of hope into this because my Hematologist has seemed to be convinced, and has convinced me, that I'm basically a ticking time bomb, whereas my naturopath has a more positive outlook on this, that the body one has is not the same body from a year ago. I'm pretty emotionally distraught and traumatized, so I needed some positive foundation, so I might be looking at this with too much faith.
Anyhow, the Histadelia meant that I had too many histamines, and that I would experience harsher symptoms due to this.
And the copper deficiency? The naturopath told me why it was important through naturopath dialect. "The body is a whole, of one thing isn't aligned than nothing is" sort of deal. I listened because I needed to listen. But when I got home
I googled copper deficiency. And according to google, copper deficiency has lead to thrombocytopenia. It's listed as a rare outcome of copper deficiency, but any possible reason is more comforting than none.
Yes, I know google isn't the most reputable of sources. But has anyone else been tested for copper deficiency?
I only started taking copper two days ago, so I don't think I'll notice any improvements right off the bat. Especially since I'm dealing with Prednisone symptoms still. And I'm aware that this might be too easy of a solution for something like ITP. But I'm going to try.
Thanks for listening