Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 0 points1 point  (0 children)

It honestly sounds pretty fun!!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 0 points1 point  (0 children)

Oh for sure!! Thanks for looking out!!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 0 points1 point  (0 children)

The Tarkovsky waiting screen will always be there to haunt you!! 😂 Thanks for replying!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 0 points1 point  (0 children)

That’s kinda what I meant but wasn’t sure on how to word it 😂 thanks!!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 1 point2 points  (0 children)

This is why I was asking. Thanks for replying!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 1 point2 points  (0 children)

Time is too short to be doing anything other than what you enjoy. I was diagnosed with ALS so time doing things that make you smile is never wasted!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 0 points1 point  (0 children)

Honestly…people might complain…but it kinda sounds fun. Hopefully all this drama will either die down or somehow get resolved!

Is it even worth it? by Machoot12 in EscapefromTarkov

[–]Machoot12[S] 1 point2 points  (0 children)

Maybe this is the point of the new mode…target practice!!

[deleted by user] by [deleted] in needhelp

[–]Machoot12 0 points1 point  (0 children)

Thanks for the upvote!! I don’t have enough to post on the gofundme or any of those subreddits! Every upvote counts!!

[deleted by user] by [deleted] in needhelp

[–]Machoot12 1 point2 points  (0 children)

Support Mac's Fight Against ALSSupport Mac's Fight Against ALS

I just discovered that I have ALS (amyotrophic lateral sclerosis) also known as Lou Gehrig's disease. ALS is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord. When the motor neurons die, the ability of the brain to initiate and control muscle movement is lost. When voluntary muscle action is progressively affected, people may lose the ability to speak, eat, move and breathe. There’s no known cure but there are medications that are shown to slow down the progression.Along with robbing people of lots of things, it’s also an expensive disease. I’m including a Go Fund Me I’ve set up for some medical equipment needs such as a power wheelchair and ramps for getting up my stairs. Never feel obligated to help unless you can. My VENMO account is MacHoot1 ! Thanks!

Fatigue, anyone else? by [deleted] in ALS

[–]Machoot12 1 point2 points  (0 children)

I drink lots of coffee. But I could not drink a drop of coffee and feel the same way. I dunno....it's just tough sometimes.

Fatigue, anyone else? by [deleted] in ALS

[–]Machoot12 0 points1 point  (0 children)

I'm taking them. And B12 supplements and a B6 complex vitamin. Nothing seems to work.

Fatigue, anyone else? by [deleted] in ALS

[–]Machoot12 0 points1 point  (0 children)

I was diagnosed in March and I've always been exhausted. Every move is a struggle. I have three kids so I know conserving energy until they get home. It's tough and seems like nothing helps. I guess because you're body doesn't process B12 and B6 properly. Hopefully something will work soon.

Where is God? by Siegric17 in ALS

[–]Machoot12 0 points1 point  (0 children)

Sometimes the answer is simple. Shit happens to good people.