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Comments (479)

If you do the Quest ANA lab with titer and reflex, you will get ICAP's (International...

https://connect.mayoclinic.org/comment/1230263/

indications of systemic sclerosis (scleroderma

Discussion: My Autoimmune Journey: From 1:5120 to 1:320 ANA

Support Group: Autoimmune Diseases

Posted: Feb 5 5:15pm

I am doing bloodwork for autoimmune problems this Thursday. I would not be at all surprised...

https://connect.mayoclinic.org/comment/1106522/

and finally her doctors landed on scleroderma

Discussion: Type 2 rosacea sufferers

Support Group: Autoimmune Diseases

Posted: Jul 16, 2024

I’m familiar with Cytoxin and Rituxin. What will you replace them with? Is your scleroderma controlled...

https://connect.mayoclinic.org/comment/954450/

Is your scleroderma controlled now?

Discussion: Lupus pain

Support Group: Autoimmune Diseases

Posted: Oct 26, 2023

Hi,Sandy For me,my statin ha no effect at all,like you I stopped taking it for 2...

https://connect.mayoclinic.org/comment/100016/

now,but I also have Raynaud’s and scleroderma

Discussion: Is there any connection with statin use and neuropathy?

Support Group: Neuropathy

Posted: Dec 24, 2017

My last labs came in with 320 platelets. I'm also 70, but no family history of...

https://connect.mayoclinic.org/comment/1382431/

have RA, osteoporosis and systemic scleroderma

Discussion: Essential thrombocythemia (ET): When to start hydroxyurea (HU)?

Support Group: Blood Cancers & Disorders

Posted: Aug 30 7:04am

Hi @paktoledo, I'm sorry to hear you are losing your rheumatology nurse practitioner. Rochester Mayo Clinic...

https://connect.mayoclinic.org/comment/907949/

and I see he specializes in Lupus, Scleroderma

Discussion: Losing a great Rheumatology nurse practioner

Support Group: Autoimmune Diseases

Posted: Aug 5, 2023

@dancing1, Interestingly @abdulhamid50 asked a similar question only yesterday. See my response above. They experience the...

https://connect.mayoclinic.org/comment/720897/

group and you also have Sjogren's, scleroderma

Discussion: Dry mouth and bitter taste

Support Group: Ear, Nose & Throat (ENT)

Posted: Jun 25, 2022

Since having Covid in 2022, (was fully vaccinated and very careful), I have been diagnosed with...

https://connect.mayoclinic.org/comment/1012174/

diagnosed with the morphea form of scleroderma

Discussion: Has anyone been diagnosed with an autoimmune disease after covid?

Support Group: Post-COVID Recovery & COVID-19

Posted: Feb 8, 2024

I have being diagnosed with Scleroderma as part of Systemic Sclerosis. Reunald's disease more then 20...

https://connect.mayoclinic.org/comment/140104/

I have being diagnosed with Scleroderma

Discussion: Scleroderma and Raynauds

Support Group: Autoimmune Diseases

Posted: Mar 1, 2017

Hi! I have absolutely no idea what specific antibodies I tested high on. I finally got...

https://connect.mayoclinic.org/comment/167826/

diagnosis this past summer - limited Scleroderma

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

Support Group: Autoimmune Diseases

Posted: Jan 10, 2020

Yes, I have had a high ANA since I was 36. I am now 74. It...

https://connect.mayoclinic.org/comment/1138767/

them to come up with my diagnosis of scleroderma

Discussion: ANA 1:160 - is it an auto immune disease?

Support Group: Autoimmune Diseases

Posted: Sep 9, 2024

Most definitely you should find a rheumatologist who specializes in scleroderma/Crest. My rheumatologist usually does a...

https://connect.mayoclinic.org/comment/251392/

rheumatologist who specializes in scleroderma

Discussion: Limited Scleroderma or CREST Syndrome: What helps?

Support Group: Autoimmune Diseases

Posted: Oct 4, 2019

I have very high autoimmune markers including lupus and scleroderma but without all the symptoms on...

https://connect.mayoclinic.org/comment/942588/

autoimmune markers including lupus and scleroderma

Discussion: Struggling with making an osteoporosis treatment decision

Support Group: Osteoporosis & Bone Health

Posted: Oct 5, 2023

@helen1000 one of my kids had an ANA of 1:160 and it is not considered significant....

https://connect.mayoclinic.org/comment/1138660/

I have very high antibodies for scleroderma ... I don't have symptoms of scleroderma

Discussion: ANA 1:160 - is it an auto immune disease?

Support Group: Autoimmune Diseases

Posted: Sep 9, 2024

Yeah, I’m not keen on it, no matter the length of time. But if it becomes...

https://connect.mayoclinic.org/comment/1102526/

years ago and now is being treated for scleroderma

Discussion: I keep relapsing when I try to get off prednisone

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Jul 9, 2024

Yes! let me share with you. "Manifestation of rheumatoid arthritis during subcutaneous allergen-specific immunotherapy with bee...

https://connect.mayoclinic.org/comment/940488/

allergy and clinical immunology Scleroderma

Discussion: Autoimmune disease induced by allergen specific immunotherapy.

Support Group: Autoimmune Diseases

Posted: Oct 2, 2023

I also had an overall increase in inflammation with Long COVID being initially diagnosed with Scleroderma...

https://connect.mayoclinic.org/comment/1202320/

COVID being initially diagnosed with Scleroderma

Discussion: Anyone experience Post-Covid Inflammatory Arthritis?

Support Group: Post-COVID Recovery & COVID-19

Posted: Jan 2 9:55am

Hi Wendy, Just finished my 2 yrs. of Forteo and got my 1st injection yesterday for...

https://connect.mayoclinic.org/comment/768902/

I have Lupus, Sjogen's, Scleroderma

Discussion: Prolia treatment for osteoporosis: What is your experience?

Support Group: Osteoporosis & Bone Health

Posted: Nov 3, 2022

COVID seemed to lead into CREST (in my case). 8/25/2022-present. Latest Labs show: elevated BUN, High...

https://connect.mayoclinic.org/comment/878254/

Obvious Scleroderma with Reynaud&#39

Discussion: Limited Scleroderma or CREST Syndrome: What helps?

Support Group: Autoimmune Diseases

Posted: Jun 14, 2023

Hi Butterfly.. Your post caught my eye especially I have family members with Scleroderma and I...

https://connect.mayoclinic.org/comment/259485/

especially I have family members with Scleroderma

Discussion: Scleroderma and severe iron in brain

Support Group: Autoimmune Diseases

Posted: May 1, 2019