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Comments (1,372)

Hi Gabe, it’s been over a year since I posted. My SOB is still here but...

https://connect.mayoclinic.org/comment/927572/

anything to do with COVID vaccine or Lyme

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

Support Group: Lung Health

Posted: Sep 10, 2023

@rivergirl8243 - I know the frustration you are going through - beyond extensive workup and testing-...

https://connect.mayoclinic.org/comment/107808/

Lyme?

Discussion: Autoimmune Diseases and Fatigue

Support Group: Autoimmune Diseases

Posted: Sep 13, 2020

Had my 3rd Reclast infusion in August. 2024. Never had side effects other than minor ache/headache...

https://connect.mayoclinic.org/comment/1170581/

then saw my PCP who ran tests (even Lyme

Discussion: Reclast side effects

Support Group: Osteoporosis & Bone Health

Posted: Nov 9 9:38am

I appreciate everyone taking time to reply and so sorry for those of you who have...

https://connect.mayoclinic.org/comment/1131603/

Resurgence of past infections, such as Lyme

Discussion: decision whether to get new booster

Support Group: Post-COVID Recovery & COVID-19

Posted: Aug 27 9:10am

The left side of my face is numb. I had an MRI to check for acoustic...

https://connect.mayoclinic.org/comment/868434/

actively if things got worse; I had Lyme

Discussion: Small Fiber Neuropathy and Face?

Support Group: Neuropathy

Posted: May 29, 2023

Something that most doctors won't pick up as an illness or refuse to admit it is...

https://connect.mayoclinic.org/comment/237199/

explore to help you better understand Lyme

Discussion: Lyme Disease

Posted: Jun 27, 2019

I agree with Lyme Disease. Did you know that there is a lab in California that...

https://connect.mayoclinic.org/comment/949741/

I agree with Lyme Disease. ... California that does nothing but test for Lyme ... it came back positive for a type of lyme

Discussion: Chronic pain and other joint issues: Looking for answers

Support Group: Bones, Joints & Muscles

Posted: Oct 18, 2023

I get it! There are so many drugs that can help with inflammation internally that we...

https://connect.mayoclinic.org/comment/1041629/

if I get a tick bite because I had Lyme

Discussion: Long Covid and Doxycycline: Inflammation Theory

Support Group: Post-COVID Recovery & COVID-19

Posted: Mar 28 11:16am

https://connect.mayoclinic.org/comment/1084676/

Lots to do- getting blood checked for Lyme

Discussion: Looking for the best lifestyle changes to reduce symptoms

Support Group: Autoimmune Diseases

Posted: Jun 11 7:09am

Hi, I am so sorry to hear you say that there has been lack of support...

https://connect.mayoclinic.org/comment/770210/

I am being treated for Lyme/Bartonella

Discussion: Lidocaine intravenous treatment - peripheral neuropathy

Support Group: Neuropathy

Posted: Nov 7, 2022

Hi - I have suffered from neuropathy pain since I was diagnosed with Lyme disease. It...

https://connect.mayoclinic.org/comment/686534/

neuropathy pain since I was diagnosed with Lyme

Discussion: TS-HDS Antibody and Small Fiber Neuropathy

Support Group: Neuropathy

Posted: Mar 4, 2022

New member, My PMR started April 2018. At the time I was on 25mg of statin...

https://connect.mayoclinic.org/comment/649670/

caregiver put me on doxycycline for lyme

Discussion: PMR Anyone?

Support Group: Polymyalgia Rheumatica (PMR)

Posted: Oct 30, 2021

Thank you for your posts about the TG6 test. I, too, saw the webinar with the...

https://connect.mayoclinic.org/comment/996679/

to be ruled out for MS and Lupus, Lyme

Discussion: Anti-tranglutaminase-6 antibody test - Gluten Sensitivity Test

Support Group: Digestive Health

Posted: Jan 13 2:04pm

@sundance6 - It is not unusual for Fibromyalgia to coexist with illnesses such as Lyme arthritis...

https://connect.mayoclinic.org/comment/330959/

to coexist with illnesses such as Lyme

Discussion: What are Tests and Medications for Fibromyalgia?

Support Group: Fibromyalgia

Posted: Dec 29, 2020

I get auras without headache as well. I do not take any medications because I am...

https://connect.mayoclinic.org/comment/1104425/

Have you been tested for Lyme?

Discussion: ANA 1280 now ANA 2560

Support Group: Autoimmune Diseases

Posted: Jul 12 1:34pm

Had my 3rd Reclast infusion in August. 2024. Never had side effects other than minor ache/headache...

https://connect.mayoclinic.org/comment/1170462/

then saw my PCP who ran tests (even Lyme

Discussion: bone pain for months after Reclast Infusion

Support Group: Osteoporosis & Bone Health

Posted: Nov 9 7:09am

I have taken Ambiem for many years without side effects. Recently I switched to Lunesta with...

https://connect.mayoclinic.org/comment/98557/

The symptoms of both Lyme Disease and

Discussion: Chronic Pain members - Welcome, please introduce yourself

Support Group: Chronic Pain

Posted: Aug 1, 2019

HI @parus. No I haven't had any side effects at all. The only thing was being...

https://connect.mayoclinic.org/comment/173466/

I haven't had Lyme Disease.

Discussion: Gabapentin use for neuropathy

Support Group: Neuropathy

Posted: Dec 30, 2017

Your comments make so much sense. I had Lyme Disease in 2016 and get flare ups...

https://connect.mayoclinic.org/comment/1092818/

I had Lyme Disease in 2016 and get flare

Discussion: Long Covid and Doxycycline: Inflammation Theory

Support Group: Post-COVID Recovery & COVID-19

Posted: Jun 23 9:05pm

Oh, my. I totally understand as I'm going through something similar right now and it is...

https://connect.mayoclinic.org/comment/163168/

I finally found out I had Lyme Disease

Discussion: Anyone had serotonin syndrome? What causes it? How to prevent it?

Support Group: Depression & Anxiety

Posted: Aug 10, 2017