ME/CFS – search | You searched for comments

I was focusing on ME/CFS because that ... they also knew I had MALS and told me ... I was left to manage my ME/CFS symptoms ... They had me mostly on a BRAT diet, then

Discussion: Median Arcuate Ligament Syndrome (MALS)

Support Group: Digestive Health

Posted: Mar 18, 2018

@2011panc , thank you for responding. My doctor is indeed compassionate and I value her. I...

https://connect.mayoclinic.org/comment/254279/

The doctor I have now diagnosed my ME ... /CFS two years ago and I'm trying

Discussion: How to talk to my doctor & share research/knowledge I have found?

Support Group: Just Want to Talk

Posted: Mar 14, 2019

I developed gluten intolerance when I was diagnosed with ME/CFS in 1984. Over time, I seemed...

https://connect.mayoclinic.org/comment/1287296/

intolerance when I was diagnosed with ME ... /CFS in 1984. ... My ND told me about 00 soft wheat flour

Discussion: Long COVID and gluten sensitivity

Support Group: Post-COVID Recovery & COVID-19

Posted: Apr 22, 2025

Hi Mark, I am in the process of diagnosis with Dr. Farhad at MGH for SFPN...

https://connect.mayoclinic.org/comment/210953/

David SYstrom at BWH for SFPN from the ME ... /CFS pulmonary angle.

Discussion: Looking to connect with people who have non-diabetic neuropathy

Support Group: Neuropathy

Posted: Feb 9, 2019

I'm responding to webdog and many others who have been in conversation about Myalgic Encephalomyelitis/Chronic Fatigue...

https://connect.mayoclinic.org/comment/792406/

/CFS) My journey has been long. ... /CFS. ... /CFS as she was doing medical research ... /CFS. ... /CFS.

Discussion: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) treatments

Support Group: Just Want to Talk

Posted: Jan 4, 2023

@debbienod I and most of us here can totally relate! I’m on my 3rd neurologist -...

https://connect.mayoclinic.org/comment/1368267/

But I also have ME/CFS so I’ve had a ... I never recovered and developed ME/CFS ... answers, especially since I also have ME ... /CFS which has rendered me disabled

Discussion: Do I need to deep dive diagnosis?

Support Group: Neuropathy

Posted: Aug 11, 2025

Those sound very similar to the symptoms I had leading up to my diagnosis of ME/CFS...

https://connect.mayoclinic.org/comment/246664/

had leading up to my diagnosis of ME ... /CFS aka Chronic Fatigue Syndrome. ... getting better, my pediatrician sent me

Discussion: Teen with weird mono...or not?

Support Group: Infectious Diseases

Posted: Aug 14, 2019

I dont know how anyone COULD cope well with LC. It is terrible. Very few providers...

https://connect.mayoclinic.org/comment/967190/

my own ( I have had to do this for ME ... /CFS for yrs. as I am a 46 yr. ... SURVIVOR of ME/CFS and Fibro. ... ME/CFS and Fibro. ... It will get me thru this too.

Discussion: Help! Need coping strategies for long Covid diagnosis and symptoms

Support Group: Post-COVID Recovery & COVID-19

Posted: Nov 18, 2023

Hello Natashia @nastashian, I would like to add my welcome to Connect along with @Erinmfs. You...

https://connect.mayoclinic.org/comment/615537/

Encephalomyelitis/Chronic Fatigue Syndrome (ME ... /CFS) treatments: https://connect.mayoclinic.org ... myalgic-encephalomyelitis-chronic-fatigue-syndrome-me-cfs-treatments

Discussion: Misdiagnosed multiple times I need answers

Support Group: Autoimmune Diseases

Posted: Jul 10, 2021

I’m glad to hear you’re finding help with a new provider. My first appointment with a...

https://connect.mayoclinic.org/comment/911273/

experienced by people suffering from ME ... /CFS and Long Covid. ... - Women are affected by ME/CFS at

Discussion: PHQ-9 Screening: “ Little interest or pleasure in doing things?”

Support Group: Post-COVID Recovery & COVID-19

Posted: Aug 11, 2023

Most helpful in the understanding of why more help/answers are NOT forthcoming from the Medical Profession...

https://connect.mayoclinic.org/comment/96452/

viewing of "UNREST" a documentary about ME ... /CFS on INDEPENDENT LENS---Ch. 9.