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Comments (1,314)

Hi I just joined this forum and I thought I'd share my story. I'll summarise as...

https://connect.mayoclinic.org/comment/281404/

Electrophoresis, ACE, HIV 1+2, Hep B+C, Lyme

Discussion: Undiagnosed, numbness, tingling, Muscle weakness and more

Support Group: Brain & Nervous System

Posted: Nov 13, 2019

Hi @dash99999, I'm sorry to hear your suffering - been there, done (and doing) that. As...

https://connect.mayoclinic.org/comment/138375/

Lyme disease (I was a rampant outdoorsmen

Discussion: Male, 23, Possible Autoimmune Issues, Difficult to Diagnose

Support Group: Autoimmune Diseases

Posted: Feb 16, 2017

Thx for all the great info nyx. The "doc" I referred to is a rheum. She...

https://connect.mayoclinic.org/comment/1067155/

I was not tested for Lyme's, would

Discussion: Surprised and Uncertain: Should I get a second opinion?

Support Group: Polymyalgia Rheumatica (PMR)

Posted: May 13 10:33am

It’s hard to not be validated when you know something is going on with your body!...

https://connect.mayoclinic.org/comment/1071925/

testing for underlying deactivations of Lymes

Discussion: I feel like I’m slowly dying and nobody is helping

Support Group: Post-COVID Recovery & COVID-19

Posted: May 20 9:01pm

Hi Ginger, Thank you so much for responding and for your questions and comments. I'm going...

https://connect.mayoclinic.org/comment/1077993/

('05), Fibromyalgia ('07), Lyme

Discussion: Bone marrow biopsy and/or blood tests for MGUS

Support Group: Blood Cancers & Disorders

Posted: May 30 4:13pm

I find that to be a narrow view of professions. By that definition, you’d have to...

https://connect.mayoclinic.org/comment/1053876/

Finally, people with CFS/Fibromyalgia/Lymes

Discussion: Keys to a Successful Doctor's Appointment

Support Group: Visiting Mayo Clinic

Posted: Apr 19 3:34pm

My Doctor told me Covid can bring on phychosis.Undiagnosed autoimmune diseases,lymes and other viruses that covid...

https://connect.mayoclinic.org/comment/1073553/

phychosis.Undiagnosed autoimmune diseases,lymes

Discussion: Psych symptoms post COVID

Support Group: Post-COVID Recovery & COVID-19

Posted: May 24 12:29am

It is so sad to see so many of you who are in constant pain, like...

https://connect.mayoclinic.org/comment/1060266/

discovered that they have long term Lymes ... I have had Lymes several times. ... after being under good conrol, I had a Lymes ... I keep wondering if my Lymes has been

Discussion: How to deal with constant pain for years

Support Group: Chronic Pain

Posted: May 1 10:39am

Hi Geraldine! Sorry things are so tough! I think we can all relate — definitely sucks...

https://connect.mayoclinic.org/comment/1055438/

As for my path, Bartonella, Lyme’s were

Discussion: Are Antivirals and/or Antibiotic cocktails the Cure for LC?

Support Group: Post-COVID Recovery & COVID-19

Posted: Apr 22 3:02pm

Lower back, both buttock cheeks, now add hips, back of thighs to back of calves to...

https://connect.mayoclinic.org/comment/1071357/

I am now on doxy for Lyme's since ... tested positive (although I've had Lyme