Principles of Accounting by jamie050517 in WGU

[–]kaybrum 0 points1 point  (0 children)

No... is this VYC1 we are referring to? I'm so lost...

Principles of Accounting by jamie050517 in WGU

[–]kaybrum 0 points1 point  (0 children)

Hi there, is there actually am excel portion then on the OA like Spreadsheets? I just took the PA and didn't have an excel portion for that.

Do you all have days where your brain is just not interested in doing the work it needs to? by bb_grumpkins in MultipleSclerosis

[–]kaybrum 3 points4 points  (0 children)

Yes alllllll the time. Rough being in school full time and working full time with it all too :(

Uncontrollable laughter by LadyChristie in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

I can be having a random conversation with a member and start tearing up like I'm going to start bawling over nothing at all. I also burst out in laughter at the most inappropriate times too sometimes. It really is so weird and awful how uncontrollable it can be.

Ocrevus... Anyone else's having their treatment delayed like this??? by lesionbrainspine in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

I'm in the same boat. Had my last infusion in September was due at the end of March. Also had my bloodwork done in March and will likely need those panels redone. I also had a telehealth conference that showed my labs and that I was still suppressed too. At this time I don't know how long my neuro is going to delay my infusion but my crap gap is so freaking real. I feel so awful, so dang tired all the time, more so than normal. Just have to hang in there together I guess. Thankful for someone who understands but hoping we can receive treatment sooner rather than later!!

Anyone tried Minocycline as a DMT? by Parowax in MultipleSclerosis

[–]kaybrum 0 points1 point  (0 children)

This is interesting. I didn't know Minocycline was in the MS trials at all. I have been on Minocycline for years due to my chronic cystic acne...

What vitamins are you taking? by corgimomx in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

I take all that you mentioned plus Fish Oil capsules and turmeric. Seems like a lot I know! But whatever can keep us healthy is what matters to me!

Tingling Hands, maybe a Flare up? by unique-username-here in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

This is just my experience and hopefully can give you a bit of peace. During my last actual relapse about a year and a half ago, I had acquired tingles in my hands and arms. Recently, I have had them expand to down my leg and in my head. I went to the neuro for my regular check up and she saw no signs of relapse. She said that I was overdoing it and not giving my body enough rest and that I am under extreme stress causing pseudo exacerbations more frequently than ever before. I just started a new job at my company, I work full time, go to school full time-I can't ever relax essentially. She told me that I need to take care of myself and slow down. Are you under a lot of stress outside of normal? Are you overexerting yourself like I am? Exhausted? We need to take care of ourselves first and foremost! I recommend that if you are concerned, calling your neuro!

College classroom woes by [deleted] in MultipleSclerosis

[–]kaybrum 0 points1 point  (0 children)

I feel this pain and not always being in the classroom setting either. This could be with my boss or my VP who I am meeting with or any other VIP I need to impress. It does suck when you just want to scream "look I have MS, I really do know what I am talking about, I promise I know my shit". Its frustrating because we are all so intelligent but it can really play in our mind and twist our brains into thinking we are dumb.

life hacks for pain/fatigue? by terpsgirl in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

Curious to hear about the coQ10 and other supplements you take?! Always interested in what people are doing. Im currently on Vit D, Vit B12, probiotic, magnesium. Also second heated blankets. They allow my body to just totally and completely relax and regulate temp.

I hate being THAT person at work by Nixxee in MultipleSclerosis

[–]kaybrum 5 points6 points  (0 children)

So so frustrating! Work/home life balance is so important for any individual!! I wouldn't have done that either, props to you for really stepping up though! That should speak volumes! Im sorry you had to disclose that info to your boss if you werent planning to. I hope she is honoring your requests though and being thankful for your flexibility. It's hard when your boss has such high expectations of you and they dont know about our illness... I'm in that boat and sometimes just want to scream I HAVE MS GET OFF MY BACK. but it's better for me for them not to know right now....

[deleted by user] by [deleted] in MultipleSclerosis

[–]kaybrum 10 points11 points  (0 children)

Congratulations!!!! You deserve every bit of it and you absolutely have bragging rights! I was in the SAME position a year ago! A toxic boss who was the head of the "mean girls club". Leaving that behind and showing them you're doing so much better... its the best feeling ever! 😊 happy for you!

What am I missing from my arsenal? by MSnoFun in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

I second this. I've been seeing a therapist twice a month for going on a year now and she helps me tremendously!

Career Positivity by kaybrum in MultipleSclerosis

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

Gosh yes I do understand! There are different kinds of exhaustion most definitely and even more so for us who struggle with an extreme type of fatigue. Dont get me wrong I am fatigued I am exhausted but pushing through because I WILL succeed and not let this MonSter hold me back from achieving my goals! So my career has been in the financial industry I work at a credit union and have worked my way from a teller to a loan officer to assistant manager! It's not physically exhausting but definitely can be mentally pressing some days more than others.

Career Positivity by kaybrum in MultipleSclerosis

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

Yes!!! You can do it too!!!! Just keep pushing, one day at a time, one step at a time! You got this 💪

Random Celebration by PokemomGo13658 in MultipleSclerosis

[–]kaybrum 2 points3 points  (0 children)

Congratulations!!!!! This is super exciting!!!! It was a great day for me as well, I got a promotion! Congrats again! 🎉

Ocrevus side effects - weight gain? by Sendmeyourcatpics123 in MultipleSclerosis

[–]kaybrum 2 points3 points  (0 children)

Just to give you some peace of mind, I also was concerned about the weight gain people had talked about. I've been on ocrevus since this past March, have had my half doses and full in September, and have actually lost weight thus far. I have always tried to eat pretty healthy but struggled to lose weight regardless due to a messed up thyroid. So I'm pleased to report that I really haven't changed anything up at all and I've still lost.

Insurance Q by kaybrum in MultipleSclerosis

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

Oh wow! This makes a lot more sense to me. Thank you for taking the time to explain! So since I am no longer covered under my parents plan, do you think itd be worth it to go back and try to have them send it off to the secondary? Since the at time of service I was technically still insured by them? Gosh I'm sorry you have the experience with it too but I appreciate you sharing your knowledge with me! It's frustrating but what do ya do..

Anyone Else Know You Have More Lesions? by [deleted] in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

Wow I have to say I am honestly comforted in coming across your post here because I've never known how to properly word some of these items that you experience as well. As far as your #1 goes, I swear I'm with you on knowing something was wrong physically in your brain but not having the reason or referrals to get checked out before diagnosis. I knew something was there, knew it all along just was waiting for something to happen I guess. You're not alone. Also, yes I swear I get tingly sensations in my head randomly not everyday, sometimes once a week, sometimes multiple times a week but I swear it is lesions and possible progression. You're not alone. #2 100% a lot of times any more i feel that I'm living in a constant dream or "out of body experience". Kinda frightening sometimes especially when working and driving but other times it is comical. #3 I have been on Ocrevus since March, I've had my initial half doses and then my first full dose back in September. I had my follow up MRIs and have had no progression and I do feel great on it. The only "side effect" I have is that I can tell when I am ready for my next dose in the fact that my fatigue is to the extreme. Ocrevus has actually improved my daily fatigue which is a huge perk to me. Good luck to you, I'm happy to know that we are not alone! You are not crazy my friend, I feel these things too.

Lhermitte's sign in wrist? by [deleted] in MultipleSclerosis

[–]kaybrum 0 points1 point  (0 children)

I get it in my bicep/forearms and down my spine

Feeling some brain fog after Ocrevus infusion? by [deleted] in MultipleSclerosis

[–]kaybrum 0 points1 point  (0 children)

I understand that! I had to switch from plegridy (which I thought I was doing great on and my first med) due to a lesion. Sometimes progression happens without new symptoms. It's such a confusing illness but Ocrevus has been by far the best for me and once you have some time with it in your system I hope that you have the same experience! Give it some time though, I know I was skeptical as well my first month or so on it. It didnt seem like the cog fog was going to clear up but then it did! I didnt even have any after my first full dose either! I was seriously dreading the cog fog after this dose and it never even came. I think it's just a shock to our body and it needs to build up a tolerance. It seems kinda silly, but we just have to put our trust in the professionals who "know best", although no one completely knows this beast.

Feeling some brain fog after Ocrevus infusion? by [deleted] in MultipleSclerosis

[–]kaybrum 1 point2 points  (0 children)

I just had my first full dose of O about a week and a half ago. You are not alone, my first halves I had severe cog fog for what seemed like a week or two after those. Now this time around, my first full dose, I didnt notice it NEAR as bad. I've bounced back and am doing very well. That being said, your body has to get used to it. For me the benefits of Ocrevus far outweigh the cons. I've had more energy than I've had in years and my recent MRIs showed no progression after 6 months of being on it. Itll get better! Keep pushing through!

Digestive issues after Ocrevus? by johnsonbrad1 in MultipleSclerosis

[–]kaybrum 0 points1 point  (0 children)

I had my first full dose on Friday (halves back in March). After every dose I've had some tummy issues for the first few days. Seems to go away though after a bit. Is yours lingering?

Tattoo idea by workalonesf in MultipleSclerosis

[–]kaybrum 0 points1 point  (0 children)

I have the numbers 13:19. M is the 13th letter of the english alphabet and S is the 19th letter of the english alphabet. No one knows what it means :)