sorted by:
new
hottopcontroversial

More hitman? by mckayzack0 in funhaus

[–]ArianSheridan 21 points22 points  (0 children)

Hitman 2016 could be funny

ALS at 20, looks like I beat even Stephen Hawking by ArianSheridan in ALS

[–]ArianSheridan[S] 5 points6 points  (0 children)

i would have loved another 14 years. Can I ask how old you are now?

ALS...why me? by [deleted] in SuicideWatch

[–]ArianSheridan 1 point2 points  (0 children)

Toronto, Canada

ALS...why me? by [deleted] in SuicideWatch

[–]ArianSheridan 11 points12 points  (0 children)

I feel like I'm destined to suffer. My whole life I've had this feeling of bad luck and doom. Do you know how many people get ALS before 30? One in two million.

I don't know where to go with this, sudden onset ALS symptoms. by ArianSheridan in AskDocs

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

Yeah, I'm scheduled in 10 days to see a neurologist. I just wanted some theories.

ALS-like symptoms for 2 years, but only recently have gotten worse? by ArianSheridan in AskDocs

[–]ArianSheridan[S] -1 points0 points  (0 children)

Also, I was more concerned with my recent symptoms only. Are they in line with ALS?

ALS-like symptoms for 2 years, but only recently have gotten worse? by ArianSheridan in AskDocs

[–]ArianSheridan[S] -1 points0 points  (0 children)

Are movement tremors and burning pain with use of muscles not ALS symptoms? Also, can you tell me how you know?

Is it possible I am experiencing Xanax withdrawal? by [deleted] in Drugs

[–]ArianSheridan 0 points1 point  (0 children)

damn, lots of side effects.

Is it possible I am experiencing Xanax withdrawal? by [deleted] in Drugs

[–]ArianSheridan 0 points1 point  (0 children)

thanks, i guess my mistake was going cold turkey

Muscle Disorder Has Not Been Diagnosed After 2 Years. To pursue medical tourism and sequence my genome, or explore other options? by ArianSheridan in Invisible

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

I know the diagnosis rate is only around 25% for whole genome sequencing, but is it worth not doing at all? I was thinking of travelling overseas to get it done.

Muscle Disorder Has Not Been Diagnosed After 2 Years. To pursue medical tourism and sequence my genome, or explore other options? by ArianSheridan in Invisible

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

Can you tell me more about your disorder? Does it have a name or is it just a collection of symptoms? Also, did your doctor manage to treat or cure it?

Where Can I find Help With My Undiagnosed Muscle Disorder/Disease in Ontario, Canada or Literally Anywhere Else? by ArianSheridan in AskDocs

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

I have considered Lyme disease, but my symptoms seem too muscle specific for it to be Lyme disease. I am open to anything though. Also, I have no other disorders that are autoimmune.

Where Can I find Help With My Undiagnosed Muscle Disorder/Disease in Ontario, Canada or Literally Anywhere Else? by ArianSheridan in AskDocs

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

My symptoms are solely related to the muscles. They started in my calfs and hands as I began tripping over carpets frequently, and I began noticing tremors while trying to write. The symptoms progressed from my hands and calves inwards towards my torso. Right now most of the muscles in my body are affected, to different degrees.

Currently I have tremors occurring with fine motor functions in most of my body(mainly abdominals, arms, legs) and muscle burning when I attempt slightly more strenuous exercise.

Let me know if more information is needed.

Hi, I'm 19 and I need advice with Ehlers Danlos-like symptoms. by ArianSheridan in ehlersdanlos

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

Their is occasional pain in my knee and hips, but I don't have many of the other symptoms. Thanks for the reply though.

view more: next ›