There was a website mentioned on facebook called. MCTD.ORG; it is a non profit organization used on wordpress. So far it looks very basic word type of forum it seems like the website started recently and is unknown to those who need to see it.
The MCTD page is up and running. It is made to create a basic understanding of the disease that I was able to gather all in one page.
I may post an Q&A blog if I need to clarify any questions that anyone may have. Page: /mctd.html |
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About this Dragonfly WarriorMy name is Miriam and I have chronic illness that is invisible to others. My autoimmune disease is called Mixed Connective Tissue Disease (MCTD) and I have Fibromyalgia. This is my page of my journey of how I am progressing. We are the warriors of the butterfly under this mask, |