I was just diagnosed with MCTD and there is so very little available as to what to expect and alternative treatments, US or Asia or European based. I am a 49 yr old male, may have had a few symptoms of the disease over the years, nothing of great consequence. Any advice is appreciated.
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Posted by ATL
I was just diagnosed with MCTD and there is so very little available as to what to expect and alternative treatments, US or Asia or European based. I am a 49 yr old male, may have had a few symptoms of the disease over the years, nothing of great consequence. Any advice is appreciated.