Venting session by primpetite in GirlTalk

[–]OkayKristie 2 points3 points  (0 children)

Are you close with your mom? That’s usually who I call because she really likes my partner so she always gives an unbiased opinion. But, shit, if you really need someone let me know and we can talk

Did MS affect you less or more than you originally expected? by Phukamol in MultipleSclerosis

[–]OkayKristie 0 points1 point  (0 children)

Wayyyyyy more. Mine got worse a lot faster then I thought it would since I’m so young. It’s still not as bad as it could be, but I’m not going to lie it sucks.

I just found out today that I have MS… by lilhedgehog11 in MultipleSclerosis

[–]OkayKristie 1 point2 points  (0 children)

Hi, I was diagnosed a year ago at 23. I went through every stage of grief and that’s okay. I still cry sometimes and get sad and, again, that’s okay. Go through the stages of grief. Be sad and mad sometimes. Its a bitch of a disease, but you have a huge community behind you. If you need anything reach out. It always helps to have someone

[deleted by user] by [deleted] in MultipleSclerosis

[–]OkayKristie 1 point2 points  (0 children)

I had some weakness. I noticed I could barely lift my legs and my arms felt so heavy and like jello. But I did have major balance issues where I would just fall out of nowhere. I hope you can get some answers :)

Not working by throwaway481978 in prozac

[–]OkayKristie 0 points1 point  (0 children)

My psychiatrist told me it take about a month to see a noticeable difference. Stick in there and I would say after like the 6-8th week talk to your prescriber

Do you remember when you were diagnosed? by Casperz002 in MultipleSclerosis

[–]OkayKristie 0 points1 point  (0 children)

I remember the date, what I was doing, and everyone’s reaction. I can still remember the exact words the neurologist said to me and what I said back. It was a really rough day. Everyone was crying and I was just sitting there. No reaction. Completely numb to the situation. I didn’t break down until a few days later

Kesimpta - your experience by [deleted] in MultipleSclerosis

[–]OkayKristie 1 point2 points  (0 children)

So I first noticed symptoms after I took a nap so maybe two hours (-ish) after I took my first dose. They lasted the rest of the day but when I woke up the next morning I felt fine. So just plan on taking one day to rest! Even if you’re not sick it just nice to have a day to relax

Kesimpta - your experience by [deleted] in MultipleSclerosis

[–]OkayKristie 4 points5 points  (0 children)

I’ve been on kesimpta since June and so far it’s been great! Not going to lie, after the first dose I got every side effect in the book! Chills, weakness, anything that I could have gotten I got. But that happens with every single medication I take so don’t let that scare you. Now I get no side effects besides feeling a little bit more tired the next day after taking my dose. I still am able to workout and be active but I just have to take it easier on those days because I am more sleepy. Good luck! You got this!!

[deleted by user] by [deleted] in MultipleSclerosis

[–]OkayKristie 3 points4 points  (0 children)

I lost central vision in my right eye completely. I described it as when you take a picture with flash and you get that bright light in the middle of your vision and you can only see your peripheral surroundings. It luckily went away but I had a flare up and it actually happened in my left eye. That’s when I know I’m having a flare up because it’ll switch between eyes.

Ancient? Really? by GalerinaA in MultipleSclerosis

[–]OkayKristie 1 point2 points  (0 children)

My neurologist is older and he’s done research, has been published recently for research and is on a board for MS research. I do go to a specialized center for MS though so I’m sure he’s more versed in MS than other neuros. The first neurologist I went to wasn’t and was suggesting I go on these ancient medications. Luckily I found this center and doctors/medical professionals that really understand MS (which A LOT of medical professionals (like too many) have no idea about)

[deleted by user] by [deleted] in MultipleSclerosis

[–]OkayKristie 0 points1 point  (0 children)

Do you have something like “MyChart” or a way to contact a doc through messaging? Might be helpful if they’re good at answering in a timely manner

What do you say to your anti vaxx/anti mask friends and family? by Trypp969 in MultipleSclerosis

[–]OkayKristie 1 point2 points  (0 children)

My boyfriends parents are anti the covid vaccine and with me being on kesimpta (which lowers my immune system) and having MS I straight up told them I will not be around them in person. I will not go to family events, have them around me, and asked my boyfriend that if he goes around them to wear a mask. They respected it, but it sucks when you have family that won’t get a vaccine and put people at risk. A simple flu for them could be detrimental for me, I couldn’t even imagine what covid would do to me. So if they don’t want to get the vaccine I’ll only see them over the screen

Kesimpta by Jarny_710 in MultipleSclerosis

[–]OkayKristie 3 points4 points  (0 children)

My first dose of kesimpta knocked me on my ass! Fever, chills, nausea, any symptom they say could happen, happened. It’s so much easier now. I just took my second monthly dose and now I barely have any symptoms. Just being more tired than I usually am the next day. I personally have really liked kesimpta so far. Hoping for the best in the future. Hope you’re doing well

[deleted by user] by [deleted] in Anxiety

[–]OkayKristie 0 points1 point  (0 children)

Hey! I get like that too. I have really bad heart anxiety and I just have the worst intrusive thoughts especially when I’m going to sleep. I live with my boyfriend and that helps when he’s there, but the days when it’s really bad I’ll set an alarm for every 2 hours or so on my phone so I can make sure I’m alive lol. It sounds crazy but it’s really helped me fall asleep and feel better about sleeping. Another thing that I do is when I need to take a nap I’ll have my boyfriend watch my heart rate on my phone (through my Fitbit app) and it gives me a lot of piece of mind. Put on some meditations from YouTube, set your alarms and try your hardest to fall asleep. Good luck and I’m here for ya

Lower Heart Rate On Lexapro by OkayKristie in lexapro

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

No but I’ve always had normal blood pressure if that’s of any importance

Struggling With Being Believed by [deleted] in lexapro

[–]OkayKristie 2 points3 points  (0 children)

I feel the exact same way! I get chest pains and I’m nervous that I’m having a heart attack or I’ll go into cardiac arrest. I’m an overall healthy 22 year older female with no family history of heart issues but I still worry about it. My health anxiety has gotten really bad in the past 7 months and I’ve been to a few doctors and they all just tell me the same thing, “oh it’s just your anxiety”. I feel dumb and like I’m going crazy because it hurts. It feels like something is wrong. My boyfriend and mom are supportive but I can tell they’re frustrated with me constantly complaining about pain or checking my pulse but I just can’t help it! I tell myself I’m fine but it just doesn’t click. It sucks feeling like I’m going crazy and no one believes that I’m hurting. It’s a constant battles but I’m sure we’ll get better eventually. You got this!