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1,039 total results
Comments (923)
I read the articles. My mom has all those symptoms. I 'll share what i know...
https://connect.mayoclinic.org/comment/71230/
Her oxygen level could not be found ... She also has lupus and i think, congested
Discussion: Pulmonary Fibrosis*
Support Group: Lung Health
Posted: Dec 5, 2017
Hi, I'm a little late to the party! I've been diagnosed with collagenous gastritis for about...
https://connect.mayoclinic.org/comment/144645/
I would just puke up what I ate. ... probably also mention that I have lupus ... It would be nice to live a more normal
Discussion: Collagenous Gastritis
Support Group: Digestive Health
Posted: Nov 14, 2017
Hello there, I have been on a long, expensive, medicine filled journey to find the cause...
https://connect.mayoclinic.org/comment/145116/
I have a diagnosis of Lupus, with normal ... edema, loss of sensation, loss of hot/cold
Discussion: Small Fiber Neuropathy: What helps?
Support Group: Neuropathy
Posted: Oct 15, 2017
Hello, new here! Hope to make some friends. When I talk to my family( I have...
https://connect.mayoclinic.org/comment/96122/
chronic pain brought on by ms and lupus ... I'm 50 and already could not stand up ... Would love to hear from anyone.
Discussion: Chronic Pain members - Welcome, please introduce yourself
Support Group: Chronic Pain
Posted: Aug 31, 2017
Hello @sandpiper09, I am sorry you are in so much pain and getting very little help,...
https://connect.mayoclinic.org/comment/146230/
medical training but if possible I would ... there are many different types of Lupus ... further information on the types of lupus ... /types-lupus/ I’m not sure if it ... If you would like to seek help from
Discussion: Tumid Lupus with SLE Symptoms?
Support Group: Autoimmune Diseases
Posted: Jul 5, 2017
Hi, kanaazpereira. My name is Cathy Hutcherson. I’m very new to Mayo Clinic Connect. Not sure...
https://connect.mayoclinic.org/comment/132930/
I also participate in the Lupus Foundation ... many ways from those who share on My Lupus ... The Lupus Foundation’s has dedicated ... members who have severe lupus as I ... but it took seven months before I could
Discussion: Stills Disease
Support Group: Autoimmune Diseases
Posted: Mar 26, 2017
So sorry for anyone else having to go through EN. One of the difficulties is you...
https://connect.mayoclinic.org/comment/114602/
While I could reproduce the articles ... weeks before I started feeling like I could ... specialists for Sarcoidosis, strep throat, lupus ... thought maybe I had something like lupus
Discussion: Chronic Erythema Nodosum & Ehlers-Danlos Syndrome (EDS)
Support Group: Autoimmune Diseases
Posted: Dec 29, 2016
I didn't drink while I had drug-induced lupus, but I can only imagine that it would...
https://connect.mayoclinic.org/comment/128293/
didn't drink while I had drug-induced lupus ... , but I can only imagine that it would ... I'm not sure how it interacts with lupus
Discussion: Alcohol and Lupus
Support Group: Autoimmune Diseases
Posted: Dec 1, 2016
oh and as for tests, I have had RH, ANA, all the typical lupus and RA...
https://connect.mayoclinic.org/comment/107376/
have had RH, ANA, all the typical lupus ... had my feet and hands x-rayed but would
Discussion: Autoimmune Diseases and Fatigue
Support Group: Autoimmune Diseases
Posted: Aug 11, 2016
Hello again, As I am taking Coumadin, the recommended antibiotic protocol includes those which interact warfarin...
https://connect.mayoclinic.org/comment/108513/
I was diagnosed with Lupus in 2014. ... and it came back negative for RA, Lupus ... At the time my mouth was so dry I could
Discussion: Autoimmune diagnosing problem
Support Group: Autoimmune Diseases
Posted: Jul 25, 2016
Hi - I'm so very sorry to hear about what you are going thru. I am...
https://connect.mayoclinic.org/comment/101779/
tests & i learned that I have CNS Lupus ... seen a Rheumatologist yet, but i would
Discussion: Nerve damage and other issues - no root cause
Support Group: Spine Health
Posted: May 7, 2016
What I have learned about auto immune disease from my experience is that there isn't one...
https://connect.mayoclinic.org/comment/90078/
Rheumatoid Arthritis and Systemic Lupus ... was a simple answer because then you would
Discussion: I have Lichen Planopilaris
Support Group: Skin Health
Posted: Mar 25, 2016
Hi @ccorrconro, and welcome to Connect. I'm glad you chose to share your story with us....
https://connect.mayoclinic.org/comment/88211/
Would you be willing to share more about ... mswanda, @conniesgore and @tedib, I would ... autoimmune disease, like Sjrogren's and lupus
Discussion: Undifferential Conective tissue disease, Sjogrens, symptoms of Lupus
Support Group: Autoimmune Diseases
Posted: Mar 9, 2016
Hi PowerofPositive: Just checking in to see how you are? I am pretty much the same....
https://connect.mayoclinic.org/comment/73389/
I have read and I wish I could quote ... I believe, there would have to be a ... There were times which I could not ... if I did not speak my mind nothing would ... drugs for this disorder as well as Lupus
Discussion: Would like to hear from people with Sjogrens
Support Group: Autoimmune Diseases
Posted: Jul 12, 2012
Hi dstone501957, I have what I think is something similar, but the pain is in the...
https://connect.mayoclinic.org/comment/1215632/
I did get a diagnosis of Cutaneous Lupus ... (due to having both Lupus Profundus ... and Tumid Lupus). ... still "flare" with overuse, cold
Discussion: Idiopathic Autoimmune Treatment For Symptom
Support Group: Autoimmune Diseases
Posted: Jan 18 11:22am