could this be lupus – search | You searched for comments

I after more than 25 years was diagnosed finally with psoriatic arthritis. It started out as...

https://connect.mayoclinic.org/comment/140111/

doctor said it it was classic book lupus ... was given the diagnosis of PSA with lupus ... when they hired us and this is all we could

Discussion: Psoriatic Arthritis: How do you manage PA and flares?

Support Group: Autoimmune Diseases

Posted: Mar 5, 2017

Hi Judy..i'm so sorry to hear about the leg pain & weakness you are experiencing in...

https://connect.mayoclinic.org/comment/88967/

I would also add that you see a rheumatogolist ... legs/calves that turned out to be lupus

Discussion: Intermittent pain in my legs from knees down. Unable to stand

Support Group: Bones, Joints & Muscles

Posted: May 11, 2016

Hi DK I'm on zoloft but am interested in how the savella works for you? I...

https://connect.mayoclinic.org/comment/73974/

new serotonin altering meds but I could ... Maybe Momentum could post one of his ... BTW I was diagnosed with Lupus for about

Discussion: Fibromyalgia: Anyone out there with the same diagnosis?

Support Group: Fibromyalgia

Posted: May 8, 2012

TMI but has anyone had anal blister that got Infected for Years I was told it...

https://connect.mayoclinic.org/comment/1260509/

to walk after blisters burst they would ... my husband passes they say I have lupus

Discussion: Looking for info on medications for Bullous pemphigoid

Support Group: Autoimmune Diseases

Posted: Mar 17 4:04pm

Some lupus patients have high anti ds DNA especially those with kidney involvement but some have...

https://connect.mayoclinic.org/comment/1239110/

Some lupus patients have high anti ds ... I would research this topic yourself

Discussion: What could my doctor be overlooking? ANA 1:1280

Support Group: Autoimmune Diseases

Posted: Feb 17 10:59am

Any deterioration should be addressed. My eGFR was stable in the 50's for a long time,...

https://connect.mayoclinic.org/comment/1223997/

drop in eGFR is from meds (I have lupus ... if I had had a more gradual drop, I would

Discussion: Newly diagnosed with CKD (Chronic Kidney Disease) and terrified

Support Group: Kidney & Bladder

Posted: Jan 28 2:06pm

Hi there from Australia. My Heart Surgeon knew i have Lupus and Fibromyalgia but due to...

https://connect.mayoclinic.org/comment/1225696/

My Heart Surgeon knew i have Lupus and ... I could not be bothered going to another

Discussion: Raynaud's Syndrome: Anyone want to talk about Raynaud’s?

Support Group: Autoimmune Diseases

Posted: Jan 30 4:01pm

I really like my rheumatologist and he is part of a large heath system with many...

https://connect.mayoclinic.org/comment/1240475/

with my rheumatologist to rule out Lupus ... That nephrologist is the one I couldn

Discussion: Choosing the right nephrologist

Support Group: Kidney & Bladder

Posted: Feb 19 8:02am

Thank you for responding, I have been on warfain, since my first stroke, in 1989, due...

https://connect.mayoclinic.org/comment/1253599/

came out that I had anti coagulation lupus ... , where I have to get my body in a cold

Discussion: Wore a heart monitor for 2 wks, due to STV

Support Group: Heart Rhythm Conditions

Posted: Mar 8 11:54pm

I apologies for the, poo,lack of, clarification and word choice...yes hoof cloven and mouth,, is animal......

https://connect.mayoclinic.org/comment/1269784/

Could you clarify what type of lupus ... Stress can bring on flare ups lupus

Discussion: Is there a cure for inflamed tongue fungus?

Support Group: Ear, Nose & Throat (ENT)

Posted: Mar 30 6:47am

heisenberg, voice is the least of it? Have you had autoimmune testing ANA for a start....

https://connect.mayoclinic.org/comment/1262587/

I would want DNA testing. ... /news/headlines/a-breakthrough-for-lupus-treatment-study-explores-car-t-cell-therapy-for-autoimmune-disease

Discussion: Is loss of balance your primary complaint with neuropathy?

Support Group: Neuropathy

Posted: Mar 20 10:10am

I don’t know what state or where you live. There are State laws to protect pain...

https://connect.mayoclinic.org/comment/1293360/

Truthfully, I would rather do medical ... Sjögrens, Lupus, Dysautonomia, severe

Discussion: Pain Pill Addiction and Neuropathy - Looking for Guidance

Support Group: Neuropathy

Posted: Apr 30 9:46am

A radiologist diagnosed me with MP in 2016 after a CT scan. 6 months later I...

https://connect.mayoclinic.org/comment/170189/

colonoscopy and found no evidence of Cancer, Lupus ... or anything else that could be underlying

Discussion: Mesenteric Panniculitis and Sclerosing Mesenteritis: Let's connect

Support Group: Digestive Health

Posted: Mar 24, 2018

My itching just started and I have had Idiopathic Progressive Polyneuropathy for a while and Lupus...

https://connect.mayoclinic.org/comment/1287184/

Progressive Polyneuropathy for a while and Lupus ... Sorry I couldn't be of help &#x1f64f

Discussion: Can chronic itching be caused by Neuropathy

Support Group: Neuropathy

Posted: Apr 21 10:15pm

@blu93 Keep up the good work on your weight loss. I need to really work on...

https://connect.mayoclinic.org/comment/1273344/

; My mom had heart disease, RA, lupus ... I’m sure I would have much more energy

Discussion: Calf Pain for over 3 years with no diagnosis

Support Group: Bones, Joints & Muscles

Posted: Apr 3 12:05pm

@elmarie @gingerw A cancer diagnosis is scary but especially a rare aggressive one at such a...

https://connect.mayoclinic.org/comment/1308039/

partly because they both have severe lupus ... (and could help with my diet and mindfulness

Discussion: Scanxiety tips and tricks

Support Group: Cancer

Posted: May 19 5:53pm

I’ve been unwell for over 25 years. My initial diagnosis was lupus, and I was treated...

https://connect.mayoclinic.org/comment/1285831/

My initial diagnosis was lupus, and ... wine belly" because the bloating would ... By this point, I couldn’t think clearly ... Eventually, my lupus consultant admitted ... : “I don’t think this is lupus.”

Discussion: Cortisol deficiency, but with weight gain

Support Group: Autoimmune Diseases

Posted: Apr 20 7:25am

I have had some similar experiences. I tend to ask for a Western Blot Lyme test,...

https://connect.mayoclinic.org/comment/876674/

me, showed scleroderma as well as lupus ... If I were you I would find a neurologist

Discussion: Numbness, twitching, weakness but clean EMG and MRI

Support Group: Brain & Nervous System

Posted: Jun 11, 2023

I was normal and healthy before I got the first Pfizer shot. 4 days after the...

https://connect.mayoclinic.org/comment/1317082/

worse then I became so fatigued I would ... I couldn’t read without crashing or ... with MECFS; MCAS; POTS, Sjogren’s and Lupus ... Was dx with Lupus in January and the ... m hoping it’s not MS on top of the Lupus

Discussion: Internal vibrations still affecting anyone?

Support Group: Post-COVID Recovery & COVID-19

Posted: May 31 9:06am

I’m so sorry for what you’re going through and sadly, I understand. I must have shed...

https://connect.mayoclinic.org/comment/751812/

If you have drug induced lupus, you ... that worked for you, maybe Humira would

Discussion: Ulcerative Colitis questions: Confused and frustrated

Support Group: Inflammatory Bowel Disease (IBD)

Posted: Sep 20, 2022