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662d
I've been officially diagnosed with SLE for 2 years. Although my rheumatologist says it's "controlled" based on my labs I still face a lot of symptoms. Anyone else experience this when 1st diagnosed? My rheumatologist said it was all in my head.... asked me if I was having anxiety... just ignoring all my new symptoms.
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Systemic Lupus Erythematosus (SLE)
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644d
Definitely switch rheumatologists I had a doctor just like that & it led to my lupus attacking my eyes and the development of Sjorgens. A big thing that’s helped me when dealing with my lupus is having a good relationship with all of my doctors especially my rheumatologist and nephrologist. You need people that understand you & make you comfortable because lupus isn’t something that can be mismanaged. Take a breather & do a little research I promise there’s physicians that’ll take better care of you 🤎
645d
I got diagnosed with SLE in 2019 and I still struggle everyday
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I finally got a referral to see a rheumatologist and he did labs. Said I have lupus but the labs say it can't be causing my symptoms and that I'm S.O.L. I'm looking for a new one 🙃
661d
??? Yikes I mean my recommendation is to switch rheumatologists if you can
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☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision
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Bupropion
night sweats
paranoid
Valium
sertraline
palpitations
Anxiety (Including GAD)
Depression
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