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Real members of MyLupusTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
A MyLupusTeam Member asked a question 💭
Fleming County KY

I was wondering about blood tests. I have had bw at both my primary care physician and two rheumatologist which my PCP sent me to, the second because she apparently thinks the first was wrong. My PCP said the first showed ANA + and possible CTD, she suggested maybe lupus because of the symptoms. This was before the confirmed PMLE with two biopsies both pos. She then sent me to first rheumatologist who did bw and didn't give#s just said fibro. Then PCP said ok I'm going to do more bw. This time… read more

October 15, 2020 (edited)
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A MyLupusTeam Member

Thank you Alaine! I will check it out.

October 15, 2020
A MyLupusTeam Member

PMLE is polymorphous light eruption. (Allergic to the sun). I get hives, nausea, and dizziness. Lasts for days to weeks. Usually by the evening or second day after being outside for a while I have horrible pain.
Yes connective tissue disease.
I am on beta blocker for fast heart rate and I think they said pcv or something with extra and missed beats. Cymbalta for anxiety and fibromyalgia. Doesn't work for the fibro but great for the anxiety which I've had for twenty years. Vitamin D 50000 for life according to my Dr. Omeprazole for Gerd and occasional gastritis. Last steroid cream for PMLE flares. Nothing for the joints flares or headaches.

October 17, 2020
A MyLupusTeam Member

Thank you GenlancoYankowski! Checking into it along with a new Dr.

October 16, 2020
A MyLupusTeam Member

There is book - The Lupus Encyclopedia and it explains our labs, tests, etc. It is really helpful.

October 15, 2020
A MyLupusTeam Member

Thank you JoiGolinTarsitano! I will!

October 15, 2020

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