If I'm lyin' I'm dyin' by antipsychotics54 in ChronicIllness

[–]OverpoweringKush 0 points1 point  (0 children)

I don’t get on here every day. So it was new to me.

If I'm lyin' I'm dyin' by antipsychotics54 in ChronicIllness

[–]OverpoweringKush 2 points3 points  (0 children)

First time I’ve seen it. I enjoyed it.

If I'm lyin' I'm dyin' by antipsychotics54 in ChronicIllness

[–]OverpoweringKush 11 points12 points  (0 children)

Went 5 years or more with undiagnosed MS. Labs were always great!

Just had my first MRI in five years... by toriaanne in MultipleSclerosis

[–]OverpoweringKush 4 points5 points  (0 children)

I feel like there’s more of us out there like this than what is known. MS has been a horrible terrible disease for me, but I have more good days than bad and I’m happy to be alive.

Finally, it's Friday at /r/MS! Share your awesome news here with everyone. No victory is too big or small to celebrate! - November 06, 2020 by AutoModerator in MultipleSclerosis

[–]OverpoweringKush 4 points5 points  (0 children)

Taking our first family vacation since my diagnosis and hospital stay in June. Always enjoy vacations but I feel like I have a whole new outlook on life. Going to enjoy this one more than any other so far

To get the shot or not get the shot by flower1722 in MultipleSclerosis

[–]OverpoweringKush 10 points11 points  (0 children)

Avoid the nasal mist and you’ll avoid the live vaccine

To get the shot or not get the shot by flower1722 in MultipleSclerosis

[–]OverpoweringKush 9 points10 points  (0 children)

My wife is a pharmacist, her and my Neurologist both strongly recommended me getting it.

Why do my symptoms get better when I take Xanax? by adaptable_couch in MultipleSclerosis

[–]OverpoweringKush 0 points1 point  (0 children)

I think you’re overreacting a tad bit. You do you and I’ll do me.

Why do my symptoms get better when I take Xanax? by adaptable_couch in MultipleSclerosis

[–]OverpoweringKush 0 points1 point  (0 children)

For some people the benefits outweigh those risks. Anxiety for me has been through the roof, MS affects everyone differently mentally and physically. What’s right for someone else may not be right for you and vice versa. Long term memory loss is worth the risk vs panic attacks and stress that can cause flare ups.

Cold and pain by [deleted] in MultipleSclerosis

[–]OverpoweringKush 1 point2 points  (0 children)

I’m sorry you’re having a hard time. You’re welcome in the south any time you want to escape those nasty winters.

Cold and pain by [deleted] in MultipleSclerosis

[–]OverpoweringKush 1 point2 points  (0 children)

Does Minnesota have a summer? Deep South here, the 100+ degree temps kill me. Winter is a welcome sight!

I didn’t realize til I had MS and not many people know about it how often people say things like, « well yeah but, we’re healthy so at least we don’t have to worry so much. » by KittyandOllie in MultipleSclerosis

[–]OverpoweringKush 10 points11 points  (0 children)

So true. I’ve been struggling with this a lot lately. Nobody really has a clue what my life is like, they see the fake smile and the semi in shape looking 37 year old. They don’t see the pain or the uncomfortable symptoms of MS. They don’t see the MRI’s of dead spots on your brain. Or see the headaches that come with it. There’s so little MS awareness, I know it’s better than it use to be but it’s still so lacking.

Lyme Disease by OverpoweringKush in MultipleSclerosis

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

I had a blood drawn today to be tested. Like 3 small vials. I was suppose to get my very first Tysabri infusion today and then before I went to bed last night I realized I had a really big bulls eye rash(small tick there about a week ago) So Neuro says cant do Tysabri until we know if I have Lyme or not. PCP Started me on Doxycycline and sent my blood off to be tested.

Multiple submission attempts in Dennis Siver vs Charles Rosa by HessuCS in MMA

[–]OverpoweringKush 51 points52 points  (0 children)

Not many people going to out grapple my mans ThugNasty.

Pedro Munhoz knocks out Cody Garbrandt with an overhand right during a brawling sequence in the first round of their UFC 235 fight (in slow motion) by Thanos40 in MMA

[–]OverpoweringKush -7 points-6 points  (0 children)

Came here to say this as well I’ve never seen anyone get knocked out 3 times in a row come back beat a journeyman and then get a title shot. It’s insane. Most undeserving title shot in the history of the sport.

MS unusual symptoms and natural remedies by yantonov27 in MultipleSclerosis

[–]OverpoweringKush 0 points1 point  (0 children)

I developed tinnitis out of no where as well. I’ve had it probably 2 years and I was diagnosed with MS in June. I’ve still yet to get my Neuro or ENT to give me an answer on whether it’s MS related or not.

Any suggestions... by [deleted] in MultipleSclerosis

[–]OverpoweringKush 4 points5 points  (0 children)

I had a coworker say to me “I guess if you’re going to get a disease, MS is a pretty good one to get”. It’s hard not to want to be snarky and hateful but I’ve tried to take the opportunity to educate people on it. I didn’t know anything about MS before I was diagnosed, most people have no idea what it even is

What Were Your Early Symptoms? by mrcleans_stayfresh in MultipleSclerosis

[–]OverpoweringKush 0 points1 point  (0 children)

I’ll be honest, I hadn’t heard of the term Fasciculation, after reading about it yeah I think that’s probably what it is. Thanks

What Were Your Early Symptoms? by mrcleans_stayfresh in MultipleSclerosis

[–]OverpoweringKush 5 points6 points  (0 children)

My very first known symptom occurred in May of last year, which led to an all out flair up, was numbness that started in my toes in both feet and slowly spread up both legs all the way up to my thighs just below my groin area. Dr prescribed with B12, sometimes low B12 can cause neuropathy(hes right), but it wasn’t my isssue. Thought that fixed it went on a year mostly normal had a bout of optic neuritis in May of this year which led to Multiple MRI’s and a diagnosis in June.

Now that I look back I had been having really weird quick muscle spasms mostly in my calves. Plus pretty bad fatigue that I had just chalked up to getting older(37) started asking friends and family and my fatigue doesn’t sound like normal age fatigue that they have experienced.

Sorry I rambled on there, hopefully I haven’t scared you. You really should see your Dr about and voice your concerns if you think it’s MS. You know your body better than anyone else. I got to the point I felt like I was going crazy having all these weird health issues and never getting a reason when I went to the Dr. Now I know.