Connective Tissue Diseases Webinar

[@winniecash1654]

Ty. I was diagnosed with UCTD 10 years ago. Also with Hashimoto's 30 years ago. Feel like I'm dying every day. Not sick enough to get any kind of help and doctors, family and friends roll their eyes at me. It's very discouraging. The emotional pain from gaslighting is more painful than the physical symptoms.

[@TheRheumatologyPhysio]

I hope this all improves for you soon 🤞

[@lefantthepainter]

Rule out tickborne diseases. Borrelia triggered/mimicked mine and antibiotics and diet changed helped.

[@winniecash1654]

@@lefantthepainter thank you for the tips.

[@winniecash1654]

@@TheRheumatologyPhysio ty ❤️

[@janmartell9792]

I've leaned a lot from your excellent talk.I'm hoping to be referred to a rheumatologist. My Dr believes I have this, but I have to be accepted by the rheumatologist. About ten yrs ago I was diagnosed with Hashimotos.

[@TheRheumatologyPhysio]

good luck, I hope everything works out well!

[@janmartell9792]

Do Drs use medication for mixed tissue disease?

[@TheRheumatologyPhysio]

yes, it is highly variable though depending on the person and condition