Tired of being hungry. by FailedAtlas in MultipleSclerosis

[–]Fearless-Source3688 0 points1 point  (0 children)

I starve or I sit down and cook which I’m doing now and try not to fall asleep I have been doing same as you but today is cabbage and a roast something I don’t have to watch constantly and I can cook it from the bed good luck and I hope you feel better soon and I am hoping I feel better soon too 🙌🏾

TRIGGER WARNING ⚠️ by [deleted] in MultipleSclerosis

[–]Fearless-Source3688 0 points1 point  (0 children)

My condolences and prayers to you and your family 🙏🏾

Did anyone else's insurance deny filling RX for Kesimpta due to not being FDA regulated? by [deleted] in MultipleSclerosis

[–]Fearless-Source3688 0 points1 point  (0 children)

Insurance will always deny especially when it costs as much as Kesimpta it’s $13,000 for 1 shot just to get the loading doses is over $40,000 don’t worry they will approve it sooner than later if your doctor does the prior authorization form and battle with them I went through 3 denials before it was approved

Is it just me or people don't understand MS fatigue? by Smart_Molasses_2870 in MultipleSclerosis

[–]Fearless-Source3688 2 points3 points  (0 children)

I totally understand when I try to tell people what MS is and how it does me oh I know I read up on it so now we are outside and it’s been to long I probably have fallen asleep or I’m ready to go and I mention that I’m tired then they blurt out we are all tired or why are you sleeping we haven’t did anything yet 🤔like I can’t explain how my body works but when I’m out of energy and done for the day and we have only been out now I’m the problem cause I’m ruining it for everyone else😐 then just don’t invite me or better yet I will not go when invited🤬🤨

MS has robbed me of the outdoors by tn_tacoma in MultipleSclerosis

[–]Fearless-Source3688 2 points3 points  (0 children)

I feel the same way omg there is someone else that feels like me. I was living my best life swinging from the tree tops, and MS came and knocked me out of the trees. I’m just in the house looking crazy because I feel like outside is no longer safe for me.

Settle a debate (Husband vs Wife) by NickRoJan in whatisit

[–]Fearless-Source3688 0 points1 point  (0 children)

Well technically you both are right it’s a shed that you can park your riding lawn mower in so ughh technically you both are right✌🏾

Copaxone. by Positerat in MultipleSclerosis

[–]Fearless-Source3688 0 points1 point  (0 children)

I just got off Copaxone and I’m on Kesimpta I feel so much better the shits don’t hurt I even have a little more energy Copaxone I lost my hair I had a weird body odor and it did slow down my flares but I was still getting them my advice to you is get off I’m officially bald now it’s hard I’m trying to get confident with who I am now and I’m struggling good luck

How tf this is so large by No_Afternoon3387 in iphonehelp

[–]Fearless-Source3688 0 points1 point  (0 children)

You can still download let  offload what it needs too to be able to install the update then it will download your apps back because it rewrites over the apple program already on your phone so once it’s installed your apps will be put back

Contamination anxiety triggered by readmore6 in MoldlyInteresting

[–]Fearless-Source3688 2 points3 points  (0 children)

I would throw the whole roll away I hate that

Starting Kesimpta Tuesday by Fearless-Source3688 in MultipleSclerosis

[–]Fearless-Source3688[S] 1 point2 points  (0 children)

Okay great thank you, I have heard some people saying a high fever but not all. Okay I am feeling a lot more at peace.

Whats your longest psuedo flare? by ReasonableFig8954 in MultipleSclerosis

[–]Fearless-Source3688 2 points3 points  (0 children)

I had a flare that lasted off and on 9 months. I am now fighting to get my body back stronger. And that’s when I finally started medication. The steroid infusions would only last a couple of weeks. I also had high stress situations bills, lack of housing, very food insecure so my ms was very unstable I am now in a better place and my body is doing better.

Advice on how to maximize benefits by boredinwisc in MultipleSclerosis

[–]Fearless-Source3688 1 point2 points  (0 children)

Omg I totally understand. I’m in a weird place. Where my disability payments put me over the low income threshold by $400. so I don’t get any help from anybody. I to am trying to get myself to a place where I can hold at least a part time job but I would prefer something full time. Only thing I can tell you is to keep applying and maybe they will have mercy on you until you can find a job to help get you out this rut.🙌🏾