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1,052 total results
Comments (946)
Hi. Kerry here. Just came back today from first visit with what i have to say...
Couldn't make a fist. ... Couldn't cross my legs. ... immediately commented on my hands which I would ... and said he thought I did have lupus
@paktoledo: I have a friend with Lupus and she has neuropathy in her hands and feet....
@paktoledo: I have a friend with Lupus ... For her, it is part of her Lupus. ... I would ask your doctor if your symptoms ... are related to your Lupus. ... guess is your symptoms are likely from Lupus
Support Group: Autoimmune Diseases
Posted: Feb 4, 2023
Definitely not acceptable. When I was first suffering from PMR, hardly able to walk, felt like...
daily to alleviate symptoms until I could ... My first wife had Lupus, we eventually ... when the average life expectancy of Lupus
Support Group: Autoimmune Diseases
Posted: Jan 27, 2023
@aceofstars Welcome to Mayo Clinic Connect. Feeling like you have been left out from a diagnosis...
When I was diagnosed with Systemic Lupus ... result led the doctor to what they would ... Systemic Lupus is considered a " ... Also, a complete physical would be an ... what Mayo Clinic has to say about lupus
Support Group: Autoimmune Diseases
Posted: Jan 25, 2023
Thank you, John. I have looked at this list before and can't say any of them...
My Lupus test has always vacilated between ... I would like others to share what their ... So what could it be?
Posted: Jan 15, 2023
None of my business but I'll share I an NOT vexed for my Auto Immune I...
in 7/2020 they turned me down bc of Lupus ... good and being in a clinical trial would ... from me, and again when I mentioned Lupus ... #39;m out of clinical that I think I could ... want me involved I always wondered could
Posted: Sep 12, 2022
Without markers of any kind, I am still puzzled as to how we would know we...
kind, I am still puzzled as to how we would ... with osteoporosis, osteoarthritis and lupus ... So wonder if spread to bones would be
@auntieoakley I pondered this dilemma for the overnight hours, and how to respond. As a fellow...
when I was diagnosed with Systemic Lupus ... there was no definitive testing for lupus ... not spoken up when I did, the one dr could
Support Group: Autism (ASD)
Posted: Jun 13, 2022
Let me tell you my story which might help you. I was having horrible nerve and...
since I was 13 and not one doctor could ... to go for counseling because they could ... He said I either have Lupus, MS or HNPP ... And again not one doctor could figure ... I could be laying down and all of a
Support Group: Brain & Nervous System
Posted: Dec 9, 2021
I was told that I could not make an appt at this time for lupus/Ms symptoms....
I was told that I could not make an ... appt at this time for lupus/Ms symptoms ... I would like to get an appt at Mayo
I would see if one of your neurologist, or even your primary care would make a...
I would see if one of your neurologist ... , or even your primary care would make ... Cleveland Clinic or any other major place would ... one point, they diagnosed me with lupus
Support Group: Brain & Nervous System
Posted: Jul 3, 2021
That's good to hear, very inspirational indeed. In retrospect we always try to justify what's happened...
often there's very little that could ... regarding low folate in patients with lupus ... no longer believe I have PRS, but lupus
Hi John, I joined Mayo Connect because I kind of think something else is wrong besides...
besides what has been diagnosed and would ... me when I showed up with cutaneous lupus ... on more hydroxychloroquine than I would
Support Group: Depression & Anxiety
Posted: Jun 1, 2021