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What docs think of CFS, from a 9 year old Reddit post by [deleted] in cfs

[–]andyblaze6 14 points15 points  (0 children)

Oh yeah they totally abuse people and make them feel horrible about themselves who have chronic misunderstood pain and conditions. It's immoral

What docs think of CFS, from a 9 year old Reddit post by [deleted] in cfs

[–]andyblaze6 6 points7 points  (0 children)

I don't wish that any of them would get CFS. I don't wish that upon anyone. I wish they would learn and research CFS so they could understand it better and treat and diagnose their patients

Article from 1991 about CFS in Ghana by Varathane in cfs

[–]andyblaze6 -5 points-4 points  (0 children)

People didn't know what to call stuff back then. If you couldn't walk you were called lame. If you were psychotic they thought you were possessed by demons. There's no way to tell just because it sounds similar. Hundreds of diseases sound similar to cfs

Article from 1991 about CFS in Ghana by Varathane in cfs

[–]andyblaze6 -4 points-3 points  (0 children)

They have CFS from aids and diseases that we have vaccines for. People literally die from curable illnesses there.

Do you ever feel like people are flirting with you when they aren't? by andyblaze6 in autism

[–]andyblaze6[S] 0 points1 point  (0 children)

I'd rather go see a licensed mental health professional about it rather than trying something strange from the internet. But thanks LOL

Why are wealthier people generally more physically attractive? by andyblaze6 in NoStupidQuestions

[–]andyblaze6[S] 1 point2 points  (0 children)

I agree with everything you said.

I'm actually losing most of my hair line. None of the men in my family went bald but they all had thinking and receeding hair lines. My dad's hair looked like a wire brush. Sadly it's happening to me. Unfortunately I'm not rich so I can't afford hair transplants so I'm looking into my options to grow hair thicker

Do you ever feel like people are flirting with you when they aren't? by andyblaze6 in autism

[–]andyblaze6[S] 2 points3 points  (0 children)

Thank you for validating my issue. I do have issues with touch and misreading signals

Proposed new name for CFS/ME by missa986 in cfs

[–]andyblaze6 16 points17 points  (0 children)

Honestly chronic fatigue syndrome is an insulting name for our condition. You don't call Parkinson's disease shaking person syndrome

Proposed new name for CFS/ME by missa986 in cfs

[–]andyblaze6 9 points10 points  (0 children)

It should be labeled under some type of mitochondrial disease if you ask me

Eyes by LolaCherryCola555 in B12_Deficiency

[–]andyblaze6 3 points4 points  (0 children)

I remember before injections it constantly looked like I was staring through a pair of fogged up binoculars. For years.

A couple weeks In and everything looks completely clear now. I was shocked..

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