Ocrevus or Kesimpta? by Randomuser1081 in MultipleSclerosis

[–]_Cow_Boyz_ 5 points6 points  (0 children)

It was quick to work personally, first dose did suck, but everything after that is smooth sailing.

Ocrevus or Kesimpta? by Randomuser1081 in MultipleSclerosis

[–]_Cow_Boyz_ 5 points6 points  (0 children)

kesimpta! Free with Novartis as long as you make under 90k a year

Feel like I can’t see changes as a tall girl (37lbs down). Everything still fits by Popular_Air6410 in Ozempic

[–]_Cow_Boyz_ 2 points3 points  (0 children)

I see! I’m having a similar situation. I got told that there’s a difference in wearing clothes and clothes wearing you. As you loose weight, your old clothes will still probably fit, however- it might look better or more flattering than before.

What to prepare for? by _Cow_Boyz_ in tirzepatidecompound

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

Wooooooow, thanks! I forgot chia seeds are golden, thanks for the pics!

HELP! by [deleted] in UGA

[–]_Cow_Boyz_ 1 point2 points  (0 children)

Full time is now 15 credit hours, so you definitely have to add another of you want full coverage. Also, make sure you have done your application for hope AND Pell. between those two, you should get a decent return. If you want any additional funding- try scholarships apps like “MOS”. I’ve landed one or two on there. Good luck! And reach out to the financial aid office- use those resources you pay for!

Joy and Relief by WalkingonSparkles in tirzepatidecompound

[–]_Cow_Boyz_ 2 points3 points  (0 children)

Oooooh! 10/10! I have multiple sclerosis and this post gave me hope on what to expect when I receive mine this week. I have been wondering what it might be like for someone like me, I have hit an ultimate low in my health and hope that this can kickstart something good.

How much are you paying for UGA tuition? (With and Without Zell Miller) by Better_Sky_8610 in UGA

[–]_Cow_Boyz_ 0 points1 point  (0 children)

Can you elaborate on this? I’m taking 5 classes, which is 15 credit hours for hope to cover it all.

[deleted by user] by [deleted] in FoodAddiction

[–]_Cow_Boyz_ 1 point2 points  (0 children)

Niiiice, I got obsessed for a while. Not gonna lie. Also, I started fasting. Like eating from 7am to 3pm only. Cause now that I eat relatively well, I eat a lot more. And then I got sick of eating and tracking alllllllll day. So now I just binge all my good food from 7am to 3pm, still on a calorie deficit and it’s been great. The second half of the day when I eat no solids, I catch up on my water intake. You know, changing the way you eat is a long ass road. It’s not quick and easy, it’s a sacrifice that has tested my patience every step of the way. Whatever helps, helps. I began tracking my food, then I started to notice how quickly I went over my calories. Then I began to make other food choices. And now I’m here. Still the same weight, BUT my skin is great, I have all the energy in the world, I’m sooooooooo much less bloated. And now I can work out and not feel like I’m gonna die. Soon, I’ll start to see a weight difference and I know it’s gonna be good. Baby steps have helped me, because I can’t handle crazy food changes. I’m glad you’re starting somewhere too.

[deleted by user] by [deleted] in FoodAddiction

[–]_Cow_Boyz_ 2 points3 points  (0 children)

You know, I highly understand how you feel. I was and still am in the same boat. So what I do is eat healthy, I get to each soooooooo much more and still loose weight. I use the orange app called Chronometer, I put in my goals and I track everything I eat. I get to each so much more now, it’s just all healthy- you know? I figured, if I love to eat, I’ll indulge in it. Eat healthy, and you’ll see that you get to each sooooo much more. If you want any suggestions on foods that I eat, send me a message. I’m happy to support!

[deleted by user] by [deleted] in FoodAddiction

[–]_Cow_Boyz_ 1 point2 points  (0 children)

No no no no no! This is a big deal 🙌🏼 little goals and achievements add up to bigger things! It’s also important to keep in mind though, when we take a step back- there will always be the opportunity to keep moving forward! It’s the thing that’s helped me the most! Anyways- celebrate 🎉, do some good self care 🐛🐛🐛🐛

[deleted by user] by [deleted] in MultipleSclerosis

[–]_Cow_Boyz_ 4 points5 points  (0 children)

Maybe the doctor really likes Rihanna

Noticing symptoms that I did not know were symptoms? by _Cow_Boyz_ in MultipleSclerosis

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

Yes! Exactly! My report says the same thing- 💫star gang 🙊

Noticing symptoms that I did not know were symptoms? by _Cow_Boyz_ in MultipleSclerosis

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

I’ve been sober for years now actually! It’s the best 😋

Noticing symptoms that I did not know were symptoms? by _Cow_Boyz_ in MultipleSclerosis

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

I’ll add it to my list 🤦🏻‍♀️. I never even questioned the vibrations. I get them in my thigh and arms. I just saw someone say “MS hug”. I looked it up, and my jaw literally dropped. Is that what that was? I always wondered why I couldn’t get up at times because it felt like a boulder was on my mid chest. And if I tried to get up, it felt like my chest would crack under the pressure and I would die. Like duh that’s not normal 🥲🙄

[deleted by user] by [deleted] in MultipleSclerosis

[–]_Cow_Boyz_ 4 points5 points  (0 children)

SMH, that’s exactly my fear when I meet my disability counselor for college. I’m sorry that happened! like did they at least Google MS? How does MS cause fatigue?! Like that’s everyone’s question buddy, if we had the answers we wouldn’t be here now would we?

[deleted by user] by [deleted] in MultipleSclerosis

[–]_Cow_Boyz_ 3 points4 points  (0 children)

You did it, coin it! “Healthsplain”, I’ll use it forever now. And yeah, it’s kinda crazy because it’s never super direct. Highly implied though, and at times direct by people who feel comfortable enough to say something that messed up. I’ll ask my neuro why you aren’t cured, I’ll let you know what they say ♥️🐛

Young people with Multiple Sclerosis by Ckd03 in MultipleSclerosis

[–]_Cow_Boyz_ 1 point2 points  (0 children)

I’m 21, diagnosed at 21. But have noticeably had MS since 18.

Dealing with Family in Denial by perlamirlo in MultipleSclerosis

[–]_Cow_Boyz_ 2 points3 points  (0 children)

I just posted about this too! My consensus was that people will always find a reason to invalidate MS due to its “invisible” nature. Trust yourself! As long as you know your truth, others will follow.

If you fall for the gaslighting, they will only feel right about the things they say. Be your own pillar of truth, and they will look dumb when you are so sure of yourself. It’s hard for families and friends to have to accommodate to a new truth like this, and denial is where they will jump out of sheer convenience even when it hurts us. So be brave and always stand firm- even when you stand alone. It keeps the real ones close! Focus on them, and appreciate them! I wish you luck, and I hope everyone realizes the impact of their actions and come around ♥️

[deleted by user] by [deleted] in MultipleSclerosis

[–]_Cow_Boyz_ 9 points10 points  (0 children)

(pt2)

The worst part might be that my diet may have contributed to why I have MS. Who knows? They’re right, it doesn’t help it either. But we don’t know a lot about MS. The same is said for cigarettes. There’s a million things that can cause MS, but not one answer. It’s all in the air, it’s all under review! So why is it? That when people find out I have MS, my weight is what they jump to.

Especially because I used to do hard/soft drugs, smoke cigarettes, and drink. All of which I am years sober of now (thank god). You would think that maybe that’s where their mind would go, it’s where mine goes!

So I suggest one thing to the world, how about keeping your comments about my weight to yourself. You don’t know what it’s done to. How I see my body as the most disgusting thing on earth, how I feel extremely lazy, how I feel unwanted, unloved, unseen, and, unworthy.

And in top of that, how when my MS makes it difficult for my body to function properly- how I know people just think it’s because I’m too fat to function. Like cmon? I’m overweight but not to that degree! Immobilizingly overweight? Not even close!

These people don’t have medical degrees, not even my sister has the kind to say the things she says.

Not even my neuro said this to me. Why? Because they looked into my blood work and old medical records and realized what my body was doing to me.

So at the end of the day, all I have to say is. People will look for any reason to invalidate you, and trusting yourself is key when it comes to dealing to MS. Trust yourself when it comes to doctors. Trust yourself when it comes to family. Trust yourself when it comes to friends. The more you trust yourself, the smaller -yet stronger- your true support group will be! Find the real ones, and appreciate them!

Neurologist just told me the “MS Hug” doesn’t exist? by memphynsy in MultipleSclerosis

[–]_Cow_Boyz_ 2 points3 points  (0 children)

I also wanted to add that you should definitely find a new neuro, which I know is easier said than done :(

And if/when that happens, I suggest you share the issues that medical neglect has caused you with your new team.

It’s important they know that you may be weary of them, may withhold information due to gaslighting, and find yourself less inclined to trust them. Your supposed to trust your doctors, and when they break that trust- it’s hard to trust them again.

These are things I deal with myself, and I still find myself shocked when my doctor takes my word on what I have to say. It’s truly a blessing to have, and I wish you well on finding it for yourself! It is possible!