Idk if I have Lupus?
Posted , 4 users are following.
I'm really just looking for opinions. I don't know for sure of I have Lupus but I've seen ever specialist and the last one is a rheumatologist. I've been having these symptoms since May 2017. Lowgrade fever (when I wake up 97.6. by evening 99.8.), headaches, hair loss, fatigue, pain in muscles (mostly neck shoulder), lightheaded, sensitive to light, fave rash, swollen neck shoulders, anxiety (also because doctors thus far haven't diagnosed me with any thing), depression (had to step away from job because of symptoms), hard to attain water, insomnia, needes around 12 hours of sleep, high blood pressure
During last summer these symptoms were 10x. Also during the summer I had excessive sweating, night sweats, dizziness, hard time attaing fluids, swollen glands( neck ), fatigue, muscle pain, muscle swelling. Headache. Lightheaded, light sensitivity
I moved from IL, to AZ and didnt have these problems the first summer I was out here (Also didn't leave house much first summer). This past summer I got a job and was more active outside during day time.
Other:
25yrs old. My great grandmother on mother's side had lupus.
I am physically obese, little exercise ( more so since symptoms), in May I had an ear infection I was put on antibiotics. In June symptoms worsened, in July they seemes to be at a worst, and August just as bad. Not as bad sept, oct, Nov, Dec (fever stays constant and some other symptoms). In that time frame I've seen cardiologist, infec disease, hermatologist, Ent. My WBC was actually slightly during time frame.( getting updated blood work soon. Also wbc went normal with doxycycline after a 2 weeks worth). Ive also been on 4 types of antibiotics since may amoxy, cpak, a 2 week of doxy then a two month doese of doxy.
Please, I am waiting to see the specialist
0 likes, 11 replies
lilian05079 justin63oh
Posted
Hi justin63oh
Have you been tested for inflammation in the body? tests include ESR Erythrocite Sedimentation Rate blood test...CRP C-Reactive Protein blood test and ANA Anti-Neuclaic Antibody blood test also a dsDNA gene test which can indicate lupus... .i imagine you have had these tests if you were referred to a rheumatologist. It may me you have a thyroid problem..'hypothyroidism'..have you been tested for that? What tests have you had?...why were you referred yo Rheumatologist?..best wishes...
justin63oh lilian05079
Posted
I have not had any of those tests. My Primary was looking for more bacteria/viral and infections which is why I stayed on those antibitoics for months. I was referred to the rheumatologist because she or any of the other specialist can't find a reason for my elevated Tempature and I took pictures of the rash on my face. Other wise when I have my dr apps in the morning the rash is not present or most the other symptoms. In the morning I feel my best almost normal by 3pm 4pm 5pm I feel the worse. Thank you for the info I'll ask about these tests!
justin63oh lilian05079
Posted
So HEP PANEL ACUTE,
EBV PANEL,
HEP B CORE Ab, TOTAL
MUMPS VIRUS ANTIBODY IgM
LYME
COCCIDIOIDES
ANGIOTENSIN I ENZYME
THYROID PANEL
CBC
HEP B SURF
TSH HIGH SENSITIVITY
METABOLIC PANEL
WEST NILE
LIPID PANEL
HEMOGLOBIN
MRI OF NECK THYROID
CHEST XRAY CAT SCANS
lilian05079 justin63oh
Posted
Yes most those tests were for infections and thyroid. Go back to your doc and request the tests i have mentioned in my reply..my best wishes to you...
margaret22116 justin63oh
Posted
It is like the symptoms of Lupus but problem is a lot of auto immune disorders have similar symptoms. How to pin it down is the problem. But I also think that full blood screening is necessary and include a look at vitamin b12. Even if borderline that can be very problematic.
Also difficult is the fact that you can have these disorders and bloods can be unremarkable. Mine often are. Lots of doctors won't act under these circumstances. Hope for a good specialist who will monitor your symptoms properly.
justin63oh margaret22116
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margaret22116 justin63oh
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I had a long treatment which ridded me of some of my more troubling symptoms.
justin63oh margaret22116
Posted
Im glad to hear your treatment helped!! I don't hope I have Lupus but it would be a relief to finally get diagnosed so I can begin a treatment plan. I feel like this might be the right direction because ive exhausted every other route.
margaret22116 justin63oh
Posted
margarida67433 justin63oh
Posted
lilian05079 justin63oh
Posted