Scleroderma

I have hd Scleroderma for 7 years with two Bone Marrow Transplants.  Can anyone give me an insight on a treatment you are or have used that has worked.

[floridagirl11]

Hi, I just saw your post. I am currently in the process of receiving a diagnosis of some sort of auto-immune disorder. All I know is that I have "lupus-like" symptoms and several ANA-related tests have come back as indicative of Scleroderma or SLE.

Still, there's no reason to wait around when I can start taking some precautions myslef. I am currently eating according to my Blood type and let me tell you, I feel MUCH, MUCH better! I fully believe that diet is connected to the way we feel. A good book I can suggest to you is "Live Right for your Blood Type." You can check it out here: http://www.dadamo.com/.

Make sure if you order it though, you get the Live Right for your Blood Type, not the Eat Right for your Blood Type. The Live Right is a newer version of the book and also recommends different exercises according to a person's blood type. What's more, the book deals with people that are affected by autoimmune disorders and things you can do in those situations. If you do not know what blood type you are, or if you are a secretor or a non-secretor, there are testing kits available for you to order and you can do the tests at home. I highly recommend you trying this diet, I think you will be pleasantly surprised!

Also, as far as a treatment, check out this website that I found particularly interesting about a girl who was given stem cells to reverse her Scleroderma. It has been about 10 years and she has totally had all ill-effects reversed:

http://www.geocities.com/kirstinwallin/isurvivedscleroderma.html

You can email her directly from her site.

Take Care and God Bless,

Hope