VAERS reporting of symptoms after COVID-19 vaccine
I filed a VAERS report online describing my experience of contracting Polymyalgia Rheumatica after receiving the Pfizer vaccine.
Interested in more discussions like this? Go to the Post-COVID Recovery & COVID-19 Support Group.
Here is the Web Site for those who wish to look at it. https://www.hrsa.gov/cicp/
There are a number of Covid claims filed, but no record of resolution/payment I could find yet. You can see the table here: https://www.hrsa.gov/cicp/cicp-data#table-2
Here are the standards for payment under CICP: "The CICP is the payer of last resort and can only reimburse or pay for medical expenses or lost employment income that are not covered by other third-party payers. To date, the CICP has paid compensation for 29 CICP claims, totaling more than $6 million. An additional 10 CICP claims were eligible for compensation after a review of the required medical records and documentation; however, in these cases there were no eligible reported medical expenses or lost employment income for the CICP to compensate." So it would cover uninsured medical expenses and lost income for those who can prove that the vaccine caused their illness. It does not cover pain and suffering, sorry to say.
Does Mayo have a special program to help Long Haulers with their symptoms? The University of Utah Medical Center just started a program designed to help folks in your situation.
I am so sorry to hear you are still suffering symptoms for so long. I would lie to welcome you to Mayo Connect, a community of people living with a wide variety of diseases and conditions, who support each other along the way. We try to be informed medical consumers, and our own best advocates in our care. We are not medical professionals, so not able to provide medical advice. We can tell you what has worked for us (or not) and provide you with information and conversation about your questions.
If you want to read about how some people on Connect are dealing with "long haul" Covid, click this link: https://connect.mayoclinic.org/discussion/long-hauler/
Here is a link to a group called the Survivor Corps, which can help you find some help locally. Please do not be afraid because Covid is still active - it is important to get your own health under control: https://www.survivorcorps.com/
Here is some info from Mayo about long-term effects: https://www.mayoclinic.org/diseases-conditions/coronavirus/in-depth/coronavirus-long-term-effects/art-20490351
I think you need to find a doctor to address your ongoing symptoms. I know it is hard to look for a new doc, but it sounds like your son needs you, and you need to get help for you so you can help him. Do you have a friend or pastor who can help you to find a doctor?
Sue
@alanbruce here is a link to more information about Mayo Clinic's program.
- COVID Activity Rehabilitation Program (CARP) at Mayo Clinic:
https://connect.mayoclinic.org/blog/post-covid-recovery/newsfeed-post/covid-activity-rehabilitation-program-carp-at-mayo-clinic/
Are you considering such a program?
my comment was for one of the people who were hurting as a longhauler although my son in law is a long hauler
Ty. I will check it out
Thank you yes the pastor is the best bet. We here in missouri are in a hot spot of the delta variant of covid. Im staying home for now but i will telephone him. Thank you
“Jumpstart her immune system” with a Mrna gene therapy with zero long term studies as to the effects on healthy folks, let alone someone with PMR...
Sounds like a recipe for Russian roulette with a single shot rifle.
I would suggest she reads ALL The pros and cons for these vaccines before making this possibly life altering choice.
I’m in Kansas City. We’re definitely in trouble!
May I ask what your symptoms have been?