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2,451 total results

Comments (2,265)

I have had dry eyes and issues with dry nasal passages. For the eyes, liquid tears,...

https://connect.mayoclinic.org/comment/309504/

I have MCTD, with a touch of sjogrens

Discussion: What causes the loss of mucus membrane?

Support Group: Diabetes & Endocrine System

Posted: Jul 9, 2020

I have already done Cancer 2x. The 2nd time was very different. I was diagnosed with...

https://connect.mayoclinic.org/comment/111481/

dry mouth and eyes so I wondered if Sjogren

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

Support Group: Autoimmune Diseases

Posted: Jul 1, 2020

Hi Sue! Do you have RA? I do and it’s just been such an experience. Pain...

https://connect.mayoclinic.org/comment/215579/

I also have Sjogrens and 1 vocal cord

Discussion: New Diagnosis of MAC/MAI & I'm scared

Support Group: MAC & Bronchiectasis

Posted: May 1, 2020

@becsbuddy - I did not express myself correctly! The dryness of my mouth and little saliva...

https://connect.mayoclinic.org/comment/111465/

little saliva when I had symptoms like Sjogren

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

Support Group: Autoimmune Diseases

Posted: Apr 14, 2020

I do have ILD and it was caused by Sjogren's. I have one lobe of my...

https://connect.mayoclinic.org/comment/299842/

I do have ILD and it was caused by Sjogren ... my lung that is gone/dried out from Sjogren

Discussion: Asthma or interstitial lung disease

Support Group: Lung Health

Posted: Apr 6, 2020

Would appreciate having a Sjogren’s group.

https://connect.mayoclinic.org/comment/145564/

Would appreciate having a Sjogren’s

Discussion: Rheumatoid Arthritis (RA) - Introduce yourself and meet others

Support Group: Autoimmune Diseases

Posted: Mar 23, 2020

Hello. I came across this discussion group and read this post and immediately connected to your...

https://connect.mayoclinic.org/comment/167825/

My GP suspects Sjogrens Syndrome, with

Discussion: What can cause ANA titre of 1:2560?

Support Group: Autoimmune Diseases

Posted: Jan 10, 2020

I have it every night really bad. I wake up when it starts to clog my...

https://connect.mayoclinic.org/comment/210151/

sure) I also have a disease called Sjogrens

Discussion: Dry mouth: Any ideas on how to help?

Support Group: Ear, Nose & Throat (ENT)

Posted: Dec 10, 2019

Hi, I never heard of SOJGRENSNEURO? Yes I have almost the same as you. Rheumatologist told...

https://connect.mayoclinic.org/comment/1276890/

Rheumatologist told me there is nothing for SOJGRENS

Discussion: Information Sojgren's Syndrome

Support Group: Autoimmune Diseases

Posted: Apr 8 7:24am

That’s highway robbery! Unbelievable! I have primary Sjögren’s disease too. I’m using Restasis and Miebo. I...

https://connect.mayoclinic.org/comment/1213284/

I have primary Sjögren’s disease too

Discussion: Does anyone have any experience with MEIBO (PF) drops for dry eyes?

Support Group: Eye Conditions

Posted: Jan 15 8:39am

https://pubmed.ncbi.nlm.nih.gov/10922951/ I too get mouth sores on Imuran and I am diagnosed with Sjogrens. I think...

https://connect.mayoclinic.org/comment/1023068/

on Imuran and I am diagnosed with Sjogrens

Discussion: Anyone else dealing with painful mouth sores and burning mouth?

Support Group: Autoimmune Diseases

Posted: Feb 26, 2024

I took that medication, made me not be able to breathe, did better without. And I...

https://connect.mayoclinic.org/comment/1230570/

And I was at a Sjogrens group in Fairfax

Discussion: I have Sjogrens and dryness is progressively getting worse.

Support Group: Autoimmune Diseases

Posted: Feb 6 9:08am

Tricyclic antidepressant. It’s an older antidepressant and the newer ones are SSRI’s less side effects. I...

https://connect.mayoclinic.org/comment/714514/

It appears I may also have sjoygren’

Discussion: Endless withdrawal from benzos and pregabalin

Support Group: Depression & Anxiety

Posted: Jun 5, 2022

I don’t know about “laziest”, but I agree that getting the correct Diagnosis and then finally...

https://connect.mayoclinic.org/comment/1020122/

diagnosing and treating my multiple Sjogren ... Best Wishes to you on your Sjogren’s

Discussion: I have Sjogrens and dryness is progressively getting worse.

Support Group: Autoimmune Diseases

Posted: Feb 21, 2024

You've had some good sugestions to follow up on. And we all hate to see someone...

https://connect.mayoclinic.org/comment/1220847/

Also. as someone with Sjogren's

Discussion: my question, Small Fiber Neuropathy, moving bowels, urinationg a lot

Support Group: Autoimmune Diseases

Posted: Jan 24 6:24pm

I also have terrible pain in my feet and it is awful. Some hard spots on...

https://connect.mayoclinic.org/comment/1221072/

But I do have sjogrens and SFN I’m not

Discussion: Feet Arthritis, no cartilage left & bunions

Support Group: Bones, Joints & Muscles

Posted: Jan 25 7:45am

Hello suetex, Very difficult moving bowels so I think somehow pressing on my bladder? It's awful....

https://connect.mayoclinic.org/comment/1221582/

Sojgrens , I drink so much, I try not

Discussion: I have Sjogren's neuropathy of my legs. Anyone try Rituximab?

Support Group: Neuropathy

Posted: Jan 25 4:05pm

Hi @lindaray. You’ve certainly been through the wringer with little ‘ol tooth #3 with a new...

https://connect.mayoclinic.org/comment/1220753/

triggered an auto immune disease such as S’ ... jogrens symdrome.

Discussion: crown is making saliva thick and dried. Feels like peeling.

Support Group: Autoimmune Diseases

Posted: Jan 24 4:03pm

I feel bad for you...you have it much worse than me (for now). Exercise is recommended,...

https://connect.mayoclinic.org/comment/1219865/

For me: sjogrens symptoms without you ... sjogrens antibodies, yet high rheumatoid

Discussion: How do you cope with Mixed Connective Tissue Disease (MCTD)?

Support Group: Autoimmune Diseases

Posted: Jan 23 2:29pm

I developed several autoimmune conditions from Covid/vaccine. It started with antiphospholipid syndrome (clotting disorder). I developed...

https://connect.mayoclinic.org/comment/995676/

and was diagnosed in May 2023 with Sjogren ... to advocate for myself in getting a Sjogren

Discussion: Living with LPSVS (long post-COVID vaccination syndrome)

Support Group: Post-COVID Recovery & COVID-19

Posted: Jan 11, 2024