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Working With Fibro
A MyFibroTeam Member asked a question 💭

This question is for everyone. I want to know who has a job, who doesn't, and how Fibro affects you working personally.

posted January 26, 2017
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A MyFibroTeam Member

DanyPatino I ask because I am a part time waitress, and even being on my feet for 5 hours makes me insanely exhausted and in so much pain. My boyfriend doesn't really understand how bad Fibro is, so without telling you all that up front, I wanted to get an unbiased opinion so he could see how others truly are affected by their Fibro.

posted February 9, 2017
A MyFibroTeam Member

Hi! I do not have a job and I find it very difficult to have one.
I get really sick if I do too much or if I do something for too long.
It affects me for the next few days because I feel like I need to replenish or something.
And with fibro, you never know what day is going to be a bad flare day so it makes me anxious.
I did recently apply to three places in the mall but no one called me back sooooo.. Anyway I am a model and I create art and have an etsy shop so those are my main sources of income (which isn't very steady 😣) But the art is my way of working from home!

posted January 27, 2017
A MyFibroTeam Member

@by A MyFibroTeam User Around 12 yrs ago I worked at the USPS on the computer and other things. I began to hurt in my back and in the neck area. I felt so bad that when I came into work people would look at me and say, you don't feel good do you? I stood it as long as I could and the doctor took me out of work. I filed for SS Disabilty and the USPS also. I was turned down by SS the first time and with no money to put in my part of the budget I stressed even more. There were some precious people in the USPS who gave me some of the Leave and that helped so much because you get paid when you are absent. I finally got an Attorney that worked with disable people and tried to get their money for them. The second year I was approved by USPS and after that SS approved me. It would be impossible for me to work now. I have Chronic Fatigue also. I barely get anything done and do not go out very often! Hugs
John 3:16

posted January 26, 2017
A MyFibroTeam Member

I'm only able to work 6-9 hours a week for now. And I am 23. Trying it bit by bit. It's very rough, especially working with children. I love it! But it's really hard being around a lot of noise as it intensifies sensitivies and pain.

posted February 20, 2017
A MyFibroTeam Member

I work part time and if Fibro is cranky or I am stressed I can't think or concentrate.

posted February 7, 2017

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