Hi there everyone,
I recently went to a rheumatologist because my GP suspected sjogrens syndrome, as far as I know the blood tests are not back yet but from what I have read they aren't 100% for diagnosing sjogrens anyway. The reason for my post, I had the letter back from their department and it says on it in the "diagnosis section" - sicca symptoms. This has left me a little confused, so is the rheumatologist saying that I have sjogrens or not? I was also told I have joint hyper-mobility spectrum disorder but im not sure how much this affects (beighton score of 8/9 but about a year ago I started with spasmodic dysphonia possibly caused by this but not 100% sure).
Any advice would be really helpful just hate how doctors don't seem to clarify anything they just leave you with more questions.
Thank you.