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Comments (1,969)

Hi @geneseos, welcome to Connect. I have small fiber peripheral neuropathy but only have numbness and...

https://connect.mayoclinic.org/comment/157145/

> Groups > Autoimmune Diseases > Sjogrens ... /connect.mayoclinic.org/discussion/sjogrens

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Mar 21, 2019

@gloriajean... I dislike the new lady who has slid into my skin when I wasn't looking....

https://connect.mayoclinic.org/comment/248153/

Then....sjogrens.

Discussion: Five Things I Wish I’d Known Before My Chronic Illness

Support Group: Neuropathy

Posted: Mar 18, 2019

Hi Suzie . Not that I’m happy you are sick, but I find comfort knowing someone...

https://connect.mayoclinic.org/comment/254768/

I have not been classified as Sjögren

Discussion: Autoimmune attacking my lungs

Support Group: Autoimmune Diseases

Posted: Mar 17, 2019

Does anyone have a low white cell count from Sjogren's Syndrome?

https://connect.mayoclinic.org/comment/111372/

anyone have a low white cell count from Sjogren

Discussion: Sjogren’s Syndrome – Introduce yourself and meet others

Support Group: Autoimmune Diseases

Posted: Feb 23, 2019

Immune disease called Sjorgren's syndrome.

https://connect.mayoclinic.org/comment/83465/

Immune disease called Sjorgren's

Discussion: After Hep C Treatment

Support Group: Infectious Diseases

Posted: Feb 8, 2019

I have had severe acid reflux for many years. It has progressed from esophagus to mouth...

https://connect.mayoclinic.org/comment/53212/

I also have Sjogrens that exasperates

Discussion: Burning Mouth Syndrome. I have it very severe.

Support Group: Skin Health

Posted: Feb 15, 2019

Hi anniemae, I've probably said this far too many times, but...... My Neuropathies are all 'idiopathic'...

https://connect.mayoclinic.org/comment/157008/

with Lupus, Rheumatoid Arthritis, Sjogren

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Feb 12, 2019

I was diagnosed with Sjogren's syndrome it sounds very similar to a symptoms that I have...

https://connect.mayoclinic.org/comment/137340/

I was diagnosed with Sjogren's syndrome

Discussion: Undiagnosed auto immune disease, put on Leflunomide

Support Group: Autoimmune Diseases

Posted: Mar 10, 2019

hi barbara, these stories r just devastating as is my own. i am 8 yrs post...

https://connect.mayoclinic.org/comment/183037/

CVID with predominant B cell damage, sjogrens

Discussion: Post Interferon Syndrome

Support Group: Infectious Diseases

Posted: Apr 25, 2019

I had horrible side effects when I tried Cymbalta. Intestinal distress, no appetite, lost 8 pounds,...

https://connect.mayoclinic.org/comment/258708/

PS I also have Raynaud’s and Sjogren

Discussion: CAN A SPECIAL DIET BE THE ANSWER?

Support Group: Autoimmune Diseases

Posted: Apr 19, 2019

Hi there Bryan- I'm sorry to hear about your health issues. SPS is a member of...

https://connect.mayoclinic.org/comment/49585/

(SPS, Myesthinia Gravis, Sjogren&#39

Discussion: Stiff Person Syndrome: Want to connect with others

Support Group: Brain & Nervous System

Posted: Sep 4, 2019

Hello. I am a 71 year old woman who has dealt with fibromyalgia for most of...

https://connect.mayoclinic.org/comment/98666/

I have Sjogren’s and Raynaud’s syndromes

Discussion: Chronic Pain members - Welcome, please introduce yourself

Support Group: Chronic Pain

Posted: Sep 3, 2019

Thanks for your reply. The doctor suspects MDS but I also have CIPO and Sjogren's and...

https://connect.mayoclinic.org/comment/274263/

suspects MDS but I also have CIPO and Sjogren

Discussion: What was your experience with bone marrow biopsy?

Support Group: Blood Cancers & Disorders

Posted: Sep 3, 2019

Hair loss with sjogrens disease with itching and flaking in scalp. Hair falling out daily after...

https://connect.mayoclinic.org/comment/818075/

Hair loss with sjogrens disease with

Discussion: HaIt loss with sjogrens disease

Support Group: Women's Health

Posted: Feb 27, 2023

@cpd54 What finally got your doctors to give you a diagnosis? Do they also know about...

https://connect.mayoclinic.org/comment/848747/

https://sjogrens.org/blog/2021/tips-for-gastrointestinal-gi-complications-sjogrens

Discussion: Sjogerns and gastroparesis

Support Group: Autoimmune Diseases

Posted: Apr 24, 2023

I developed deep aching in both feet and lower legs less than 3 hours after receiving...

https://connect.mayoclinic.org/comment/753537/

primary care doctor (who treats me for Sjogrens

Discussion: Shingrix and peripheral neuropathy

Support Group: Neuropathy

Posted: Sep 25, 2022

If you have Sjogren’s and neuropathy, you skin can itch.

https://connect.mayoclinic.org/comment/851905/

If you have Sjogren’s and neuropathy

Discussion: Question about Sjogrens and discomfort in legs. Also skin feels itchy

Support Group: Autoimmune Diseases

Posted: Apr 30, 2023

OMG, I too have Sjogren's and osteoporosis. Aside from the dental issues with osteo drugs, I'm...

https://connect.mayoclinic.org/comment/852874/

OMG, I too have Sjogren's and osteoporosis ... about side effects triggering more Sjogren

Discussion: What helps improve osteoporosis without medication?

Support Group: Osteoporosis & Bone Health

Posted: May 1, 2023

I’ve not been diagnosed with PMR, but after reading some of these post, I feel like...

https://connect.mayoclinic.org/comment/855740/

feel like I’ve been misdiagnosed with Sjogerns ... maybe are helping with the PMR and Sjogerns

Discussion: How did your PMR begin?

Support Group: Polymyalgia Rheumatica (PMR)

Posted: May 7, 2023

I fully believe stress was the instigator of my autoimmune problems. It began to be recognized...

https://connect.mayoclinic.org/comment/855343/

unprecedented step in testing for Sjogren

Discussion: Diet & PMR.

Support Group: Polymyalgia Rheumatica (PMR)

Posted: May 6, 2023