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698 total results

Comments (635)

I have the heart rate the dizziness/vertigo? the ringing on my ears when the blood flow...

https://connect.mayoclinic.org/comment/766900/

on legs when standing, pale fingers Raynuds

Discussion: How common is POTS after long COVID exposure?

Support Group: Heart Rhythm Conditions

Posted: Oct 29, 2022

I feel like the word thing is a daily word. Used in every day conversation. Person...

https://connect.mayoclinic.org/comment/776348/

I also have Lupus, sjogrens, and Raynauds

Discussion: How did you know? Aphasia

Support Group: Brain & Nervous System

Posted: Nov 22, 2022

Hi @tb0010 and welcome to Mayo Clinic Connect. I wanted to introduce you to @boconn89. I...

https://connect.mayoclinic.org/comment/742829/

through this link: MCTD, Fibromyalgia, Reynauds ... connect.mayoclinic.org/discussion/mcdt-fibromyalgia-reynauds

Discussion: MCTD, Fibromyalgia, Reynauds

Support Group: Autoimmune Diseases

Posted: Aug 28, 2022

Hello. This is a middle of the night writing so please forgive any errors or oddities....

https://connect.mayoclinic.org/comment/742559/

Initially diagnosed and treated as Raynauds

Discussion: Small fiber neuropathy - tongue

Support Group: Neuropathy

Posted: Aug 28, 2022

Hello @jessf, Welcome to Connect. Sorry to hear that you have more than neuropathy going on....

https://connect.mayoclinic.org/comment/797222/

living-with-neuropathy-welcome-to-the-group/ -- MCTD, Fibromyalgia, Reynauds ... connect.mayoclinic.org/discussion/mcdt-fibromyalgia-reynauds

Discussion: Anyone here dealing with peripheral neuropathy?

Support Group: Neuropathy

Posted: Jan 15, 2023

Hi everyone. I was diagnosed by my dermatologist back in 2016. I went to the vascular...

https://connect.mayoclinic.org/comment/796944/

various tests on me and diagnosed w me Reynauds

Discussion: Anyone out there with Erythromelalgia?

Support Group: Autoimmune Diseases

Posted: Jan 15, 2023

Hi, for the burning of hands and feet my neurologist has me take an extra gabapentin,...

https://connect.mayoclinic.org/comment/834281/

feet and hands have always been- told Raynaud

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Mar 30, 2023

I just saw this post and thought to myself, "maybe I am not going crazy because...

https://connect.mayoclinic.org/comment/838327/

autoimmune disorder, along with the obvious Raynaud

Discussion: Sjogren’s and Loss of Taste and Smell

Support Group: Autoimmune Diseases

Posted: Apr 5, 2023

I only have Erythromelagia on both feet. The cream Rhofade that I put on my feet...

https://connect.mayoclinic.org/comment/679676/

GERD and Raynauds.

Discussion: Peripheral Neuropathy vs. Erythromelalgia

Support Group: Autoimmune Diseases

Posted: Feb 11, 2022

Hello does anyone have Erythromelalgia of the face? I have SFN of the hands legs feet...

https://connect.mayoclinic.org/comment/678820/

I also have Raynaud's in hands and ... livedo reticularis is getting worse, Raynauds

Discussion: Peripheral Neuropathy vs. Erythromelalgia

Support Group: Autoimmune Diseases

Posted: Feb 8, 2022

Alpha LIPOIC ACID might help. Go on the Internet and look for 'Dr. Jay Cohen'. He...

https://connect.mayoclinic.org/comment/670472/

I also have raynauds and neuropathy.

Discussion: Anyone out there with Erythromelalgia?

Support Group: Autoimmune Diseases

Posted: Jan 13, 2022

I have had raynauds since 25. I am 80. Have developed several other autoimmune diseases. There...

https://connect.mayoclinic.org/comment/697033/

I have had raynauds since 25. ... My grandson has inherited raynauds.

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

Support Group: Autoimmune Diseases

Posted: Apr 8, 2022

Hi, I'm 60 and was diagnosed with small twitch sensory neuropathy (diagnosed from a skin biopsy...

https://connect.mayoclinic.org/comment/696549/

the neuropathy because she suspected Reynaud

Discussion: Chronic Pain members - Welcome, please introduce yourself

Support Group: Chronic Pain

Posted: Apr 6, 2022

Hello RA friends, I have been taking Humira pen every two weeks and methotrexate eight tablets...

https://connect.mayoclinic.org/comment/694152/

Attacks of Raynaud’s, Sjogren’s.

Discussion: Can methotrexate and/or hydroxychloroquine make RA worse?

Support Group: Autoimmune Diseases

Posted: Mar 29, 2022

I also have a Medtronic pain pump. I am just wrapping up my first year with...

https://connect.mayoclinic.org/comment/656676/

addition I have rheumatoid arthritis, Raynauds

Discussion: Pain pump, I have one, how about one for you?

Support Group: Chronic Pain

Posted: Nov 22, 2021

I’ve always believed healthy eating is the best way to live, and certainly my diet continues...

https://connect.mayoclinic.org/comment/656147/

ended up with PBC, Sjogren’s Syndrome, Raynaud

Discussion: Multiple autoimmune diseases

Support Group: Autoimmune Diseases

Posted: Nov 20, 2021

Sorry I meant to say 6 mg of boron three to four times a day -...

https://connect.mayoclinic.org/comment/159317/

(which is controlled by turmeric), Reynaud

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Nov 20, 2020

Hello. I have neuropathy pn from head to toe. 67 yr. old female, myriad of diseases...

https://connect.mayoclinic.org/comment/158556/

Hands in rolled up heat pad for Raynaud

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: May 8, 2020

I can totally relate. The cold feet is probably raynauds syndrome. I have that. The fast...

https://connect.mayoclinic.org/comment/202827/

The cold feet is probably raynauds syndrome

Discussion: Mysterious shortness of breath: What has helped you?

Support Group: Lung Health

Posted: Apr 9, 2020

@sunnyflower, @bethunger Helllo, Ladies. We 3 have many things in common, it seems. Sunny, when you...

https://connect.mayoclinic.org/comment/159782/

Sunny, when you mentioned Raynaurd&#39

Discussion: Living with Neuropathy - Welcome to the group

Support Group: Neuropathy

Posted: Mar 13, 2021