As a person living with scleromyxedema, I have created a website to share my experience with others living with this disease and to provide a forum/network of support.

I have been living with scleromyxedema for ten years, and as you may know, there is very little information about it, nor is there definitive treatment for it.

I would greatly appreciate it if you would share my website and contact information with anyone else who has this rare disease—which is often (mistakenly) thrown together with scleroderma—and who is looking for support.

Webmaster's Note: Unfortunately, Phyllis' site at scleromyxedema.com is no longer active.