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 » Who has gotten the vaccine?

 - UBBFriend: Email this page to someone!    
Author Topic: Who has gotten the vaccine?
TxLymie
LymeNet Contributor
Member # 20847

Icon 1 posted      Profile for TxLymie     Send New Private Message       Edit/Delete Post   Reply With Quote 
Just curious about how the vaccine affects those of us with Lyme. Looking to hear the positive and negative experiences so I can make an informed decision

Which vaccine did you get?
What were your symptoms if any and how long did they last?
If you haven't gotten the vaccine, why not?

--------------------
TxLymie
IgG-Negative
IgM - Postive bands 23 and 41

Other dx: 2000: Endometriosis 2009: Chronic EBV, Mycoplasma infection, HHV6, H.pylori

Posts: 297 | From Houston | Registered: Jun 2009  |  IP: Logged | Report this post to a Moderator
Mountainsky
LymeNet Contributor
Member # 51857

Icon 1 posted      Profile for Mountainsky     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hello. Yes I got it.

I was very nervous of it. You can ask ask my friends and family all last year and up to a few months ago I was petrified of getting it or thinking I'd be forced to at my job. 2 years ago I was injured by a vaccine that throw my Lyme and Co's from 0-60.

There were nights I literally wouldn't sleep because of this. Would I be discriminated against for not like traveling, going to a concert, a ballpark etc.

I started a new job 6 months ago which I absolutely love after being out of the workforce for so long from Lyme. I was afraid my hesitancy on vaccines would interfere with my job. I work in a hospital. My boss and coworkers have been so understanding!


I did my own research and talked to other people in the Lyme community who received one ( all 3 kinds) and other non/Lyme acquaintances who had autoimmune issues and they were all fine. My LLMD even said it was a good idea.

At the end of the day however it was MY decision and mine only. It should be yours too. It's your body. I refuse to get bullied into getting it or shamed for taking it either way. I did say summer the earliest I would start thinking about it.

I got the Phizer. I was fine and even cried after with relief and prayed so much right before that it wouldn't trigger something and make me sicker, or worse. I got my 1st dose on May 14th and my 2nd on June 4th. Both times minimal side effects.

The 2nd dose the sore arm lingered a bit longer but it was certainly tolerable. I had a bruise and a rash that now has disappeared (I was told this is normal happened to some of my coworkers and their family members).

I don't regret it, nope. 💚

Posts: 440 | From Massachusetts | Registered: Mar 2019  |  IP: Logged | Report this post to a Moderator
Lonestartick
LymeNet Contributor
Member # 2151

Icon 1 posted      Profile for Lonestartick     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm an old-timer around here, but have been in remission for over a decade after a decades long battle with LD & co-infections. I was nervous about the vaccine, but got it because I lost a family member to Covid 19 last year and have elderly parents.

My husband (also in remission with LD) and I both got Moderna because it was the first we could find. I had what they call the Moderna Flu symptoms with immune activation. He did also to a lesser degree. It was astonishing how all the worrisome symptoms shut off 48 hours after they started, as if someone turned off a faucet.

I would have preferred to get Pfizer because typically it seems to have fewer side effects in autoimmune patients based on what medical professionals have told friends, including one with severe MS. She had both her Pfizer without setback.

It is so nice to get back to living normally. I still shop with a mask on and wear a mask when working with transport or the clinics that do vetting. With close friends who have been vaccinated, I don't worry about it unless they have symptoms of colds or flu.

Posts: 470 | From USA | Registered: Feb 2002  |  IP: Logged | Report this post to a Moderator
daisys
LymeNet Contributor
Member # 11802

Icon 1 posted      Profile for daisys     Send New Private Message       Edit/Delete Post   Reply With Quote 
I went with the Moderna vaccine because it was the first one available to me.

I checked with LLMDs, and the one thing that stood out is that there may be a set back with the vaccine, but that's nothing compared to getting Covid-19

A friend who works in our local hospital, and so is in the middle of treating the pandemic, told me that even surviving it, it's far worse than the vast majority of those who have reactions to the vaccine.

This friend and I had decided not to get the vaccine right away. But by the time it was available, we both got it without hesitation.

People are still dying every day from this virus. Some of my healthy friends who got covid-19, and weren't sick enough to go to the hospital, are still noticing problems.

I also was reminded that LD causes the immune system to go into overdrive. So, getting the vaccine may cause reactions because the vaccine is effective.

I felt a little worse for a few days--fatigue, body aches and headaches. It wasn't anything I'm not used to. I even wondered if it was just me, and not the vaccine causing it.

We don't know if problems will show up down the road with the vaccine. But, we do know that this virus has killed many.

I respect the decision that a person makes about getting the vaccine, or not, because they know their own situation the best. They also will be the one who lives with their decision.

I'm glad I got vaccinated.

Posts: 488 | From New Mexico, USA | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
lucecaboose
Member
Member # 13058

Icon 1 posted      Profile for lucecaboose     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got the Moderna. My LLMD said not to get it but I had to. I catch everything, like most everyone here, because my immune system is shot.

My IgM is very low and in 2019 I caught the flu twice, had four colds and mono. In 2020 nothing, because I stayed home and was extremely careful going out.

With the Moderna, after the first shot I had a sore arm. After the second, it was just like having a bad Lyme day. I hurt and was exhausted, it did not make my neuropathy act up.

It showed up after six hours and lasted about 12 and I just slept it off. It was no biggie.

Posts: 42 | From Grand Rapids, MI | Registered: Aug 2007  |  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 got the Pfizer vaccine.

First dose I had a sore arm. Second dose I had a headache which lasted less than 12 hours.

No other symptoms. Did not cause my Neuro symptoms to flare up at all.

I rarely get sick so I think my immune system is pretty good, but I am sure glad I got the vaccine.

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

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

Posts: 7049 | From Illinois | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
paleogal
LymeNet Contributor
Member # 45991

Icon 1 posted      Profile for paleogal     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got Pfizer. I had 12 days of severe fatigue (which honestly I only linked it to the vaccine because it disappeared on day 12) and migraines after the first dose, then about a month of fatigue and headaches (but only when exercising) after the second dose.

LLMD said they were here for me for Lyme flare, and would prefer that (the devil we know...) to me getting covid. At the time I was working in a high risk job.

Posts: 235 | From Southern Arizona | Registered: Jun 2015  |  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 
FYI: An informative review of people's personal experiences with Lyme and Covid "vaccine" reactions. Scroll down to blog section:

https://danielcameronmd.com/opinion-low-covid-19-vaccine-trust-among-lyme-disease-patients/

Also...people with Lyme can contribute to the information base by taking the survey on Dr. Cameron's website:

"You are invited to share your experience with Lyme disease if you are at least 12 years of age and if:

You have had COVID-19
You have had the COVID-19 vaccine
You have had neither COVID-19 nor the COVID-19 vaccine
Your experience will help others living with Lyme disease in a COVID-19 Pandemic."

Additional posts re personal experiences with Lyme and the "vaccine" can be found by scrolling down on the survey page.

https://danielcameronmd.com/lyme-disease-covid-survey/

Posts: 1652 | From Earth | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
dbpei
Frequent Contributor (1K+ posts)
Member # 33574

Icon 1 posted      Profile for dbpei     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know that it is a very difficult decision for those of us with a chronic illness like Lyme - especially when you have neurological symptoms, which I do. I was afraid initially, and after doing lots of research, I eventually decided to get vaccinated, because I was more fearful of catching Covid than the risks of being vaccinated.

I have had both the first two Pfizer vaccines and recently got the booster. I had a low grade fever, pain at the injection sight, and mild flu-like symptoms the day after the booster. But the day after that, I felt back to myself. It was similar with the first two shots.

I feel very fortunate that my body handled the vaccine the way it was supposed to. I had some Lyme symptoms that have not changed following the vaccine. I have entered my information in Dr. Daniel Cameron's survey.

There is another big data pool (MyLymeData) that you can enter your information in for those suffering from lyme and getting Covid or the vaccine. So far it appears to show that those with chronic lyme are at no more risk than others in the general population to be vaccinated. This is very encouraging!

https://www.lymedisease.org/covid-19-impact-on-lyme-disease-patients/

Posts: 2360 | From New England | Registered: Aug 2011  |  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.