LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Anyone w Lyme struggle w Covid?

 - UBBFriend: Email this page to someone!    
Author Topic: Anyone w Lyme struggle w Covid?
LymeBitesCO
Junior Member
Member # 51838

Icon 1 posted      Profile for LymeBitesCO   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just wondering about other Lymie’s struggles getting over Covid?? Did anything help? I’ve been down for 11 days now.. gotta get back to work, but am so tired/woozy/intermittent low grade fevers, sore glands.. it’s got to be a Lyme reaction!? Any help is appreciated, thanks!

--------------------
LymeBitesCO

Posts: 3 | From CO | Registered: Feb 2019  |  IP: Logged | Report this post to a Moderator
hiker53
Frequent Contributor (5K+ posts)
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have friends who do not have Lyme who have been hit really hard by Omicron.

One gal, age 36, got it in June and had planned to go to grad school fulltime and work parttime as a nurse. She can only handle school parttime and no job.

Her mom, age 66, also got Covid in June and still sleeps most of the day.

Seems like Covid hits different people so differently just like Lyme does.

Sorry I can't give you a Lyme reference, though.

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 9167 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think taking lots of Vit C is good against viruses. Vit C offers electrons to free radicals and helps quench them and their damage. Take it to bowel tolerance.

Also taking Vit D is comprehensively good. I do 5000IU daily. Good to get our Vit D blood level up to at least 50 or 60, and that can be measured.

I also take Host Defense mushrooms - that's 17 dried mushrooms in a capsule - mushrooms are great for boosting WBC natural killer cell activity against viruses. I take 2 capsules in the am and pm 5 days a week. I've been very well. We can also just eat a lot of mushroom variety.

Posts: 13121 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
maryc
Member
Member # 4904

Icon 1 posted      Profile for maryc     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by LymeBitesCO:
Just wondering about other Lymie’s struggles getting over Covid?? Did anything help? I’ve been down for 11 days now.. gotta get back to work, but am so tired/woozy/intermittent low grade fevers, sore glands.. it’s got to be a Lyme reaction!? Any help is appreciated, thanks!

I tested positive twice in 2 weeks, I have finally tested negative. However, I have Lyme & EBV and I am going into my 4 week. I feel just like you? Any help
Posts: 61 | From Pembroke Pines, Florida | Registered: Nov 2003  |  IP: Logged | Report this post to a Moderator
LymeBitesCO
Junior Member
Member # 51838

Icon 1 posted      Profile for LymeBitesCO   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
On Monday I am getting a new procedure they’re offering (of course insurance doesn’t cover) now, intended for “Long Covid” symptoms.. but Long Covid is so similar to Lyme and “Post Viral syndrome”, I’m going to try it.. desperate times, eh? It’s called a “Stellar Ganglion Block”, where they give you an injection in your neck, supposed to help headaches, fatigue, brain fog, systemic inflammation type issues. We’ll see!!

--------------------
LymeBitesCO

Posts: 3 | From CO | Registered: Feb 2019  |  IP: Logged | Report this post to a Moderator
hiker53
Frequent Contributor (5K+ posts)
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
LymeBites—Please keep us updated on how the Stellate Ganglion Block works.

I wonder what is in the injection. A numbing anesthetic?

Best wishes for improvement.

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 9167 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
Frequent Contributor (1K+ posts)
Member # 49177

Icon 1 posted      Profile for Bartenderbonnie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Fascinating new treatment LymeBites CO!
Please provide sucess story when you finish as I heard this treatment could possible help chronic Lyme patients too. Good for you!

So many will robustly discuss the side-effects of the vaccines yet totally discredit the effects of the covid virus itself and the destruction it is causing to millions of the population still affected.

Long covid patients are unable to work and have a poor quality of life. We need answers. We need treatments.


Here is an interview with Dana Parish and Amy Proal (PhD Chief Officer of Long Covid Research Initiative) sponsored by Bay Area Lyme.

They discus the possibility of latent infections becoming activated and the covid virus being found in bodily tissues.

https://www.bayarealyme.org/blog/ticktective-with-dana-parish-from-long-covid-to-long-lyme-persistent-infections-drive-chronic-illness/

Dr S.P. and Dana Parish interview on Lyme and LongHaul COID

https://www.facebook.com/thechronicbook/videos/live-stream/769494304333982/

Covid and Lyme Disease Blog
https://danielcameronmd.com/covid-blog/

Posts: 3023 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hyperbaric Oxygen in Post-Vaccine and Long Haul Treatment: FLCCC Weekly Update (August 10, 2022)

https://odysee.com/@FrontlineCovid19CriticalCareAlliance:c/Weekly_Webinar_August10:7?eType=EmailBlastContent&eId=9bb0d2e8-7217-4452-865e-5c57d5326672

Posts: 1917 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
hiker53
Frequent Contributor (5K+ posts)
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
Makes sense that if Hyperbaric Oxygen can help chronic Lyme it can help Covid Long Haulers.

Phoiph, have you been able to avoid Covid? Not many have avoided Covid.

And how are you doing with your tick borne infections?

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 9167 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes...it is helpful for Covid19, Long-haul Covid, and Post-Vaccine Injury.
Posts: 1917 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I have avoided Covid, and remained healthy, gratefully.

I have been well for about 10 years.

Posts: 1917 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
hiker53
Frequent Contributor (5K+ posts)
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
My Eustachian tubes haven’t worked since I got Lyme. I bet the pressure of the chamber would make that an excruciating experience. 🙁

Glad to hear that you have avoided Covid, Phoiph. I have also.

Do you have your own chamber for treatment? Guess I am asking if you still use the Hyperbolic treatment upon occasion?

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 9167 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Many people with Lyme have (or had) eustachian tube issues (including myself), but by going very slowly they are almost always able to work through this.

There should be no pain in your ears when doing mHBOT.

Posts: 1917 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I still have my own chamber, and although I do not need to use it to stay well, I still elect to use it a couple of times a week.
Posts: 1917 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
hiker53
Frequent Contributor (5K+ posts)
Member # 6046

Icon 1 posted      Profile for hiker53     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks, Phoiph mHbot is the low pressure?

Guess I should ask these questions elsewhere as I have hijacked the thread. Sorry.

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 9167 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238

Icon 1 posted      Profile for Phoiph     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, mHBOT stands for mild hyperbaric oxygen treatment. Mild treatment is considered 1.5 ATA or lower. Home chambers go to 1.3 ATA max as per FDA.

Please feel free to join us on the Mild Hyperbaric thread.

Posts: 1917 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.