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2,714 total results
Comments (2,483)
gbrodan1945, Good morning. I was 65 yo when dx with MS. I was dx w/fibromyalgia at...
https://connect.mayoclinic.org/comment/990155/
up for various autoimmune diseases, lupus
Coleen. I have neuropathy but not sure what itis called. I have numbness in hands feet...
https://connect.mayoclinic.org/comment/817914/
forgot to mention I was diagnosed with Lupus
Thank you for the response @amandajro ! There are a few things that ring a bell...
https://connect.mayoclinic.org/comment/794351/
They were also thinking a form of Lupus
Hello @acid2come, You'll notice we moved your post to this discussion on Burning Feet Syndrome which...
https://connect.mayoclinic.org/comment/72034/
Lupus?
Hello, I can't remember if I've posted here before, but I'll introduce myself again anyway. My...
https://connect.mayoclinic.org/comment/95513/
I have just been diagnosed with lupus
@regeana I echo @kariulrich advice on speaking with your doctor. You have many things going on...
https://connect.mayoclinic.org/comment/56451/
Connective Tissue Diseases such as Systemic Lupus
I was diagnosed with Systemic lupus and Sjögren’s over 30 years ago. Up until now I...
https://connect.mayoclinic.org/comment/1242684/
I was diagnosed with Systemic lupus
You're welcome. Glad you got off the PPI I learned from my labs through my rheumatologist...
https://connect.mayoclinic.org/comment/1247503/
suspected" of causing drug induced lupus
This happened to both me and my sibling about the same year-4 years ago- we are...
https://connect.mayoclinic.org/comment/1182645/
In my case, a suspected Lupus which
Good morning!! What kind of a doctor are you using? I have appointment tomorrow with Orthopedic...
https://connect.mayoclinic.org/comment/1172714/
I have Lupus, MCTD.
I'm a DES daughter as well, and have felt there must be a connection between that...
https://connect.mayoclinic.org/comment/1321610/
disease (my thinking), or possibly lupus
I would bet this is autoimmune and your test results just aren’t showing anything yet. It’s...
https://connect.mayoclinic.org/comment/1142083/
I have lupus and had numerous symptoms
I have relapsing polychondritis, RA, systemic lupus, and CIDP. My RP is the least of my...
https://connect.mayoclinic.org/comment/1094285/
relapsing polychondritis, RA, systemic lupus
Yes side effects seem worse in weeks 2-3, for me. The medication peaks at 5-7 days...
https://connect.mayoclinic.org/comment/1057951/
I have lupus and paresthesias and a
I have all the same issues. I had an MRI without contrast and took a SAGE...
https://connect.mayoclinic.org/comment/681739/
My mom had Lupus, Sojourn.
Good Morning, I am so sorry you have not been able to get a definitive diagnosis...
https://connect.mayoclinic.org/comment/257871/
permanent damage if not medicated, but Lupus
All my ANA tests were positive. They would see the butterfly rash and order tests, then...
https://connect.mayoclinic.org/comment/221447/
called anti-smith, only shows up in lupus
Hi, Sorry to hear about all the different health challenges. I also right after Covid shot...
https://connect.mayoclinic.org/comment/1351273/
correct tests & was diagnosed with Lupus
Well as I mentioned I have fibromyalgia and have yet to find any relief from the...
https://connect.mayoclinic.org/comment/1312713/
I had Lupus about 26 yrs ago and misdiagnosed
In terms of diet I have been told to increase salt and "push protein" which is...
https://connect.mayoclinic.org/comment/1158771/
positive for scleroderma (I already have lupus
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