canceling is kindness keeping safe from covid 19 with fibromyalgia and fibromyalgia | MyFibroTeam

Connect with others who understand.

sign up Log in
Resources
About MyFibroTeam
Powered By
Real members of MyFibroTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Top 10 Search Results for "canceling is kindness keeping safe from covid 19 with fibromyalgia"

reset
Will My Fibromyalgia Put Me At High Risk For Covid-19?
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

Remember to immediately file an appeal if disability is denied. If you do not, you may forfeit back money. Good luck and perseverance.

Does Anyone Else Struggle With Auditory Sensitivity?
A MyFibroTeam Member asked a question 💭

Is it another symptom pf Fibro, to have painfully sensitive hearing, so much so it can be painful? I also get extremely overwhelmed, when there's too much noise, it can confuse and disorientate me, and do often have to leave the situation. A bit more of a description in my blog: https://thedorkdisorder.com/2023/05/07/auditory...
I don't know if this has anything to do with Fribo or if it's just something that's up with me? I have always disliked loud noises since I was a kid.

•
View reactions
A MyFibroTeam Member

Agree 100% Claire
Shopping centres and restaurants are the worst. I stopped eating out a long time ago for that reason.

Aware That COVID-19 Cases Are Rising? Masks Recommended?
A MyFibroTeam Member asked a question 💭

The CDC is recommending that people continue to wear masks even if they are fully vaccinated. They are also renewing their efforts to get unvaccinated people vaccinated.

The Delta variant is responsible for over 200% increase in hospitalizations in Missouri alone.

Regarding the unvaccinated, infectious disease physicians are describing them as incubators for new variants to develop and spread.

Please help keep yourselves and your communities safe.

Update: June 5, 2021; 147 million… read more

•
View reactions
A MyFibroTeam Member

I went to a hair stylist 3 weeks ago and I was reassuring her that I had taken every precaution by getting the double vaccine dose from Pfizer and I was wearing a surgical mask made in the United… read more

Has Anyone Had A Covid Vaccine, & Had An Adverse Reaction Because Of Our Fibromyalgia? And Which One Has Less Reactions? Physer Or Maderna?
A MyFibroTeam Member asked a question 💭
•
View reactions
A MyFibroTeam Member

I had Pfizer no problems. It’s safer to take it than get Covid as we are immune compromised.

How Easy Would It Be To Be Single And Dealing With Fibro
A MyFibroTeam Member asked a question 💭

Hi guys
This is very hard for me my partner and i have been together 8 years alot of mental abuse and him losing his head over numerous women. For the last 5 years we have had separate rooms. While on holiday he refused to share my bed and was on his phone all the time. Yep another female and he said he wants the house the car and said i cant press charges for abuse. So i started making plans with solicitor s. I said to him so you are going to throw everything away for this woman that you hardly… read more

•
View reactions
A MyFibroTeam Member

I was going to have my niece show me an apartment . But decided to begin a church near here Sunday and start counseling Tuesday. I don’t think I have the coping skills as yet.. but at least it’s… read more

Covid Longhaulers Mirror CFS
A MyFibroTeam Member asked a question 💭

This is no surprise to those of us who had been watching the news and that is that post viral fatigue is affecting more women in general, more female covid longhaulers than men, and mimics CFS.

Any reflections and experiences would be welcome to hear!

This is a very sad development and yet many of us on this site predicted this would happen, given our correlations with post viral fatigue and fibromyalgia and now with a viral based pandemic.

https://www.nbcnews.com/think/opinion/covid-lon..… read more

•
View reactions
A MyFibroTeam Member

Thank u for that informative info

Fibromyalgia Condition And Actual COVID-19 Illness Experience
A MyFibroTeam Member asked a question 💭

If you have suffered from an actual COVID-19 illness and you wouldn't mind sharing what is was like, please post here. Even if you didn't have an actual positive test result, if you are fairly sure it was COVID please post your experience. Also include what treatment you used while ill.

I am nervous about contracting COVID, but I have not had COVID or any virus or flu since being diagnosed with fibromyalgia. Since I am already in a constant painful flare, this adds to my concern.

•
View reactions
A MyFibroTeam Member

Thank you! I appreciate your response & prayers!!!

Why Do We Have Hot Flashes With Fibromyalgia?
A MyFibroTeam Member asked a question 💭

I have hot flashes and have no understanding of it. Also when the air is cold my pain will worsen, mind you when I get in my pool which is not heated the cold water gives me a pain free body.(my last swim was two weeks ago, now the pool is frozen)

•
View reactions
A MyFibroTeam Member

I assumed the hot flashes and cold flashes were from anxiety. Probably a combination. Ugh.

Does Anyone Experience Severe Pain From Blood Pressure Cuff Causes A Spike In The Reading
A MyFibroTeam Member asked a question 💭

I am becoming phobic about blood pressure readings. The cuff apparently causes a surge in Adrenalin from pain detection by our hyper vigilant nervous system. I have had readings of 220 / 120 routinely. Before Fibromyalgia my BP was always extremely low. It becomes extremely painful very quickly as the health carer keeps pumping up the pressure to get the last beat. This is a vicious cycle of increasing pain causing more Adrenaline which keeps increasing the blood pressure readings. Are there… read more

•
View reactions
Corona Virus! Is Fibromyalgia High Risk!?
A MyFibroTeam Member asked a question 💭

Hello

I cant seem to get the answers online can any one share if they have been told if fibro is high risk? I understand its not heart or lung related but is an auto immune disease

Thanks

•
View reactions
A MyFibroTeam Member

I have INCREDIBLE NEWS!! As part of my recovery from a Motorhome accident- when my beautiful M/H was wiped out, & I had whiplash & broken rib- I had some psychological therapy
Psychologist used the… read more