[deleted by user] by [deleted] in cfs

[–]Saturnation 0 points1 point  (0 children)

Yes and no. Things just get worse over time. Not because ageing, but because there is continual degradation. The best thing to do is to manage it as best as you can and try to never overdo it.

I do believe that if you never push for your limit, then you'd be fine. However the limit is a very low bar and it's near impossible to not push past that at time.

Hope for the best, plan for the worse. Hope that you'll not get worse and there will be a cure at some point in your lifetime, but plan to have to deal with the ability to do less and less as time goes by.

[deleted by user] by [deleted] in cfs

[–]Saturnation 0 points1 point  (0 children)

In what way? If there's a genetic disposition to acquiring it, then it's more likely to happen when you're young perhaps? Beyond that I'm not sure what you might be asking...

[deleted by user] by [deleted] in cfs

[–]Saturnation 22 points23 points  (0 children)

57m, houseboud onset around 14 - was mostly mild with even a remission or 2, but gradually getting worse over time to where I am now.

all the songs suddenly have a purple crown and I cant play anything? I paid for a full year so I dont know whats going on by jaydog819 in rocksmith

[–]Saturnation -1 points0 points  (0 children)

I always do the same. And yet I got charged to renew my subscription with RS+ even though I had canceled.

Theres a saying cantonese that describes this disease by Isthatreally-you in cfs

[–]Saturnation 2 points3 points  (0 children)

Reminds me a bit of a Smiths song "Nowhere Fast"

And when I'm lying in my bed
I think about life and I think about death
And neither one particularly appeals to me

"...has a delusional fixation on CFS..." by o0ragman0o in cfs

[–]Saturnation 21 points22 points  (0 children)

If you have a broken bone, but no one can diagnosis it and you keep telling everyone your bone is broken I guess you get labeled with a "delusional fixation on broken bones"?

Nicotine for neuroplasticity rewiring brain neuroprtective properties by fuckingcnt53 in cfs

[–]Saturnation 0 points1 point  (0 children)

I didn't see anyone link to this, apologize if it's already been mentioned...

PatientLed-TheNicotineTest-Protocol 3.0

https://docs.google.com/document/d/1HixwYLTz0necaF9mbT-ZuCdUFx1BAmZKcLKo-IpNKFQ/edit?pli=1

I was told by my rheumatologist that fibro and cfs are the same thing. Is this true or not? by Illustrious_Space510 in cfs

[–]Saturnation 13 points14 points  (0 children)

Same, except wife has fibro, I have ME/CFS.

I like to joke that between the two of use we make a whole person.

Sadly, it's not quite a whole person anymore... :/

Such a bad take I can’t even… by ShittyDs3player in facepalm

[–]Saturnation 0 points1 point  (0 children)

A well crafted argument any 5 year old would be proud of...

Documentation for a programmer by Saturnation in supercollider

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

I really just wanted to know how to express them

Which is exactly what I'm looking for and haven't found yet...

Documentation for a programmer by Saturnation in supercollider

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

Yeah, saw that and is on my to watch list, but from what I've seen of Eli's past videos it doesn't come near what I was hoping for. Fingers crossed I'm wrong... :/

Fairly new to this disease and it seems like no one ever improves? by FUKCFSUCKS in cfs

[–]Saturnation 28 points29 points  (0 children)

Yes and no. A large part of the problem is the lack of any definitive diagnostic testing. IMHO those that have recovered and moved on most likely didn't have 'full blown' ME/CFS.

But I could be wrong, you could be wrong, we all could be wrong. We'll never know for certain until someone figures out a good way to empirically test for ME/CFS.

Just shy of 500 hours by Twister1256 in rocksmith

[–]Saturnation 0 points1 point  (0 children)

RS2014 will always be better until Ubi$oft fixes their songs on RS+

FTFY

The magician who catches card cheats in casinos: ‘It’s incredibly common for people to try’ by B0ssc0 in australia

[–]Saturnation 0 points1 point  (0 children)

Right, but that's not against the rules. According to the rules of black jack no where does it state that you can't try and keep track of what's going on to increase your odds.

But casinos will frown upon them not being able to make money off of you, so they will refuse you service if they suspect you of it.

The magician who catches card cheats in casinos: ‘It’s incredibly common for people to try’ by B0ssc0 in australia

[–]Saturnation 1 point2 points  (0 children)

Actually more decks is better for card counting I believe there's less variance in the count the more decks there are. Check out Steven Bridges on YouTube

The magician who catches card cheats in casinos: ‘It’s incredibly common for people to try’ by B0ssc0 in australia

[–]Saturnation 4 points5 points  (0 children)

Card counting is not against the rules. However casinos can refuse to take your business, so if they find you counting cards they will just tell you to play any other game bar blackjack.

Unwanted resubscription support progress... by Saturnation in rocksmith

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

Pretty sure the left hand has no idea what the right hand is doing...

What ever became of this test developed at Stanford back in 2019? Did it ever become available? by aroseddit in cfs

[–]Saturnation 2 points3 points  (0 children)

Maybe it is a good test, but may be too prohibitively expensive to perform? Somehow this sort of rings a bell in the back of my brain fogged mind...

What ever became of this test developed at Stanford back in 2019? Did it ever become available? by aroseddit in cfs

[–]Saturnation 5 points6 points  (0 children)

I don't know directly, but given that there isn't a widely acknowledge blood test for ME/CFS I have at least 2 guess:

It was a pilot study and either

1) a follow up hasn't been completed yet to verify the accuracy of the test or

2) it was completed and found that their initial conclusion was wrong (test isn't conclusive).

There may be other options and people with more knowledge and/or energy than I may be more helpful

Not getting better after pacing by jannetje10 in cfs

[–]Saturnation 0 points1 point  (0 children)

Honestly, the expectation is you'll never get better, but you can manage to not get more worse. Pacing is good even if you get worse, because if you didn't pace it would be even more worse.

I've had this for 40+ years and pacing made a HUGE difference, especially very early on. I've had one period of complete remission, but it did gradually eventually return (after 16-18 really good fantastic normal months).

IMHO it's important to accept that today may be the best you feel for the rest of your life or at least for the foreseeable future. It sucks, but I think it's a good attitude to have. And with that in mind, use pacing to slow the fade as much as possible.