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Sjogren's likely - how to prepare for rheumatologist
Hello,
I'm a 57-year-old woman who's new to this group and just recently tested positive (78) for Salivary Protein 1 (SP1) Igg antibodies and (27) Parotid Specific Protein (PSP) Igg antibodies. I believe I've had Sjogren's for many years now but this is the first time a doctor ordered this test. I had previously tested negative on the two most common Sjogren's blood tests.
Some background is that I was diagnosed with Hashimoto's 10 years ago but have been dealing with dryness for at least 20 years. I've had bartholin cysts, dry eyes, dry mouth including mouth sores and teeth/gum issues. I've also dealt with lots of joint pain, muscle cramps, fatigue, fogginess and vertigo. I have low blood sugar issues as well and have been eating a gluten free, dairy free, low sugar diet for 25 years.
My doctor has just sent a referral to Mass General Hospital's rheumatology department and I'm worried that they'll once again dismiss my symptoms. I take very good care of myself with daily exercise and an excellent diet and doctors often say "you look great!" even though I don't feel great, particularly during flare ups. Does anyone have any experience and/or advice on how to approach this doctor's visit so that my concerns will be taken seriously?
Thanks so much for reading,
bluesmom
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@bluesmom. Welcome to Mayo Clinic. I’m glad you found the site. You asked about meeting a new doctor and being taken seriously. So much will depend on how you act. You need to be prepared, know what’s right or being told to you. Read up on Sjogren’s so will understand what is being said.
https://connect.mayoclinic.org/discussion/first-meeting-with-rheumatologist-need-suggestions/
Also, go through this discussion and you will find other suggestions.
What would you like to ask this doctor?
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1 ReactionMy big question is whether or not I actually have Sjogren’s based on the new test results and ongoing symptoms. My PCP now believes I do but I’m looking for confirmation from the rheumatologist. Also, given that I’ve already made so many lifestyle changes to accommodate my symptoms (diet, exercise, therapy, getting a less stressful part time job etc), will there be anything else I can do to improve the disease progression? Apologies. I realize my concerns are very large and fairly unanswerable. I’ll try to ask a more direct question next time I post!
Thank you.