I'm Confused On How To Keep Track Of Any Comments/replies Made To Me- If I Haven't Answered Anyone Back, My Full Apologies! | MyFibroTeam

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I'm Confused On How To Keep Track Of Any Comments/replies Made To Me- If I Haven't Answered Anyone Back, My Full Apologies!
A MyFibroTeam Member asked a question 💭

Confused about notifications on here

posted April 9
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A MyFibroTeam Member

Do you know how much money the government would lose by telling the CIA to do that lololol

posted April 10
A MyFibroTeam Member

Omg that is so much to go through!
I had a friend years ago with a similar kidney problem. Her kidneys were always loaded with stones and needing surgery often.
To go through something like that and have it's all in your head be said still 😡 gotta love that Dr ego 🙄
I was adopted, so my family medical history is kind of spotty. I did meet them during a flare up and was finally able to figure out I have psoriasis. Several types run in my family, plaque, pustular and guttate. Mine broke out like all of them and eventually started to look more like erythrotridermic, having seizures with it.
Endless food triggers. I finally have a short list of food that doesn't cause symptoms.
Chrons and Ms are in my family too. Have not tested for them so far. Stomach cancer too.
All my joints hurt too. Should get tested for Lyme after having a deer tick bite as a kid with no functional adults to help.
Every Dr I asked about it refuses to test.
Stepped on a rusty nail around the same time back then. Just about to get an X-ray of my foot now.
All the pain started after these 2 incidents.
Never had luck with any of the other nasal rinses, a lot of them made my sinuses worse. Navage is first to help.
No pressure, but I did post a link for 20$ off if you would like to try it out. I can send the link here 😁
I especially like how it just sucks all the water back out of your head lol I've been able to cut down on allergy meds with it.
It is hard to keep track of all the symptoms. I won't even domit unless I have a serious Dr to work with. It's amazing how much and how fast my fight or flight blocks a lot of it out. Pain is probably the worst symptom between joints, muscles and nerves.

posted April 10
A MyFibroTeam Member

Also, maybe the CIA could try figuring out how to mind control all our symptoms away. I know I'm not the only one to be told all of it is in our head

posted April 10
A MyFibroTeam Member

I get lots of insomnia too. Then I guess crash out from exhaustion. Stupid aliens. (That's what I call all my health problems since most have no known cause and/or very little help in controlling the symptoms.
I hope you get some rest soon!

posted April 10
A MyFibroTeam Member

The cia gathering info on mk ultra from a random pot head from a chronic illness support group is how I know lololol

posted April 13

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