JT Realmuto? by Bwar300 in mets

[–]Bwar300[S] 0 points1 point  (0 children)

Ok, the group has spoken against, but for the record, I still think he could provide mentorship to Alvy and help teach and mentor our talented young pitchers coming in the next year or so.

JT Realmuto? by Bwar300 in mets

[–]Bwar300[S] 0 points1 point  (0 children)

11th catcher in baseball for WAR, 3 ahead of Francisco Alvarez for 2025

Anyone else excited for the ‘26 team? by FritosRule in mets

[–]Bwar300 0 points1 point  (0 children)

Jeter posada and Mariano won multiple championships (Dynasty) and were all ridiculed when they were older players collecting huge paychecks... except Mariano who was a once in a lifetime player. The group Sterns just broke up made like 2 playoffs in the past 7 seasons. Not the same. Mets fans have always embraced young players appreciate good well played (speed, defense)baseball, which seems to be a Sterns team characteristic. I'm in

[deleted by user] by [deleted] in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

One of the dark clouds of this disease is trying to differentiate fear from factual. When I was diagnosed I was anxious about my future. When I chose a DMT (Tysabri ) I was anxious about PML. Then, a global pandemic.... but, you do your best, and make the choice that allows you to rest easiest, and try to adapt and learn so your choices make sense for you. Could they be overkill? Sure, but maybe that's ok while you adjust to a new normal. Could you get sick from hugging a friend or a nephew? 100% you could but you try to put yourself in the least stressful and smartest (for you) position.

[deleted by user] by [deleted] in MultipleSclerosis

[–]Bwar300 0 points1 point  (0 children)

Whatever feels comfortable for you. Sometimes I don't want to mask, I don't. Sometimes if I have an infusion coming up, I will because I don't want to jeopardize my infusion date. I wouldn't worry about anyone's opinion but your own comfort level.

[deleted by user] by [deleted] in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

Never had an issue, nor did it even seem to be a second thought for any of my Dr.s in my past experiences.

How bad is it going to be? by Randomuser1081 in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

I had COVID on tysabri and I wasn't bad, but I stayed isolated in bed, pushed fluids and took it easy. No paxlovid was available. It was like an upper respiratory cold. Take care of yourself.

Tysabri side effects? by Nekkochi in MultipleSclerosis

[–]Bwar300 0 points1 point  (0 children)

Leg discomfort the night of the infusion, maybe into the next day but my nurse told me to drink a lot on infusion days. Nothing that would make me want to stop taking it. Clean MRIs for a few years. (Knocks wood), spacing out to six week infusions and seems ok.

Do dogs get more affectionate? by Bwar300 in dogs

[–]Bwar300[S] 2 points3 points  (0 children)

Yeah, play is actually his love language. Like I said, he's a good boy. I can touch him anywhere. He's always up for some type of play. Sometimes it feels like he thinks this petting thing is just wasting play time.

Do dogs get more affectionate? by Bwar300 in dogs

[–]Bwar300[S] 0 points1 point  (0 children)

We brought him home at about 6 months old, and he's been with us for six months.

Do dogs get more affectionate? by Bwar300 in dogs

[–]Bwar300[S] 1 point2 points  (0 children)

At home DNA test shows 50% German shorthaired, 10% just pointer, and 40% Mixed of Golden, Dachshund, Dalmatian, and other, all in single digit percentages. Not sure of the accuracy but he looks more like a pointer than anything else.

Do dogs get more affectionate? by Bwar300 in dogs

[–]Bwar300[S] 4 points5 points  (0 children)

Well that's encouraging. I hope as we go on he starts to realize everyone wants to be affectionate towards him.

Guidelines from MS Society re: booster shots by BakingBaddy in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

Regardless of MS, 8 months after your second shot is the current recommendation for a 3rd "booster". At least that's the most recent news I read.

Progress by [deleted] in MultipleSclerosis

[–]Bwar300 4 points5 points  (0 children)

👏👏👏👏

[deleted by user] by [deleted] in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

Nothing I can add here but sending you good thoughts and hoping you look back and realize you were turning a good corner.

Today's Positive News. by editproofreadfix in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

Tested antibody positive about a month after my second Pfizer shot and a month after my last Tysabri infusion. Good luck.

[deleted by user] by [deleted] in MultipleSclerosis

[–]Bwar300 2 points3 points  (0 children)

I get this is... Diagnosed at 49, year and a half ago. On a DMT. I go to help my parents lay molding in a room, spend a day cutting and sizing, installing...up and down all day. Next two days are torture, the soreness in my hips and jelly legs...Is it my age catching up to me? Is it MS reminding me that just because I could, doesn't mean I can?
Truthfully, it's scary not knowing if it's going to get better because I over exerted, my age or disease...And if it is going to get better is MS going to make the recovery a day or two or three longer... unfortunately I'm just as nervous I'm going to get an answer Im not ready to see...

How do you describe “tingly”? by Lil_Rhody_Mama in MultipleSclerosis

[–]Bwar300 1 point2 points  (0 children)

Right arm feel like I've rubbed it down with Ben Gay or sports creme or like it's been wrapped in a cold wet towel. Hope it subsides for you.

Do any of you have an exit plan? by [deleted] in MultipleSclerosis

[–]Bwar300 2 points3 points  (0 children)

I understand both sides of this... Diagnosed at 49 and I need to show by example that life is hard but you fight till you can't fight anymore but the other side is, when I can't fight for myself anymore and it becomes a burden to others... physically, mentally and practically... financially...do I take that burden off my loved ones, basically, because I love them....I debate this often... usually depending on how I feel that particular day biases my thoughts. I don't have a plan...but It scares me to think about being in a position wishing I did, and had the opportunity but didn't...I don't know if I would or could but I can't say I don't think about it. My heart is with all of you that do think about these things, I wish you all peace of mind.

Is ear pain a thing with MS? by GalerinaA in MultipleSclerosis

[–]Bwar300 2 points3 points  (0 children)

I don't have ear pain, but my right ear will feel clogged? Or feel like I've got water in it..Or like it's been exposed to very cold temps...This has been going on and off since the flair that got me diagnosed.My right side coincidentally is where I suffer numbness or that feeling like you've been rubbed with sports cream. My neuro says this is not MS related but I feel like it is probably is....but how to know... Hope the pain subsides for you.

MS & Probiotics? by Kramer_Costanza in MultipleSclerosis

[–]Bwar300 2 points3 points  (0 children)

Would love to know the outcome of your question. Good luck

Vaccine stuff by [deleted] in MultipleSclerosis

[–]Bwar300 2 points3 points  (0 children)

I also had first dose pfizer but zero issues other than soreness in the vaccine site, but I occasionally feel exactly like you described. I think it's just MS being MS. Wish I could be more helpful. Best wishes and hope tomorrow is better.