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Getting over walking pneumonia. Im doing allot better. Went into A-Fib earlier today under allot of stress. Not good for my ms or my heart. How is everyone doing? Hopefully good. Missing my daughter. Long story. Still waiting for my new medicine to get started. Please pray.

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Then went back on Sunday the 13 went back by ambulance and was in the hospital till Thursday. I was in the hospital for 5 days. I was really sick. And I wasn't well. I missed you all. Nobody probably missed me and thats ok. I came back home Thursday. Good to be home. Missed everyone. How is everyone. I hope well. Me getting sick was ms related. . Had my infusion today. And im real weak. Onto of everything my caregiver is leaving today (Saturday) to go see his family all day. And leaving me alone so I'll have nobody to look after me. So if I have a emergency I will be all alone. So pray my ms or heart won't act up. I pray. Not much I can do about itill have no company. Im use to being alone. Take care you all.

Jurupa Valley, United States

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To everyone living with MS, I want you to remember this today: you are so much stronger than the days that make you feel weak. ❤️Some days, simply getting out of bed is a victory. Some days, your body may not cooperate, your energy may disappear, or symptoms may make you wonder how you will keep going. And that is okay. You don't have to be strong every second. You don't have to pretend that everything is fine.Give yourself permission to rest. Give yourself permission to have difficult days. But when tomorrow comes, remind yourself that your diagnosis does not define the beautiful person you are.MS may have changed some parts of your journey, but it does not get to decide the value of your life, the dreams in your heart, or the love you deserve.Take life one day at a time. Celebrate the small victories. Be gentle with yourself. Keep hope alive, even when the road feels uncertain.And on the days when you feel like giving up, remember: you have already survived every difficult day that brought you here. That means there is still strength within you, even when you cannot feel it.To every MS warrior reading this—keep going, keep believing, keep taking care of yourself, and never forget that your story is still being written. 🌷💙You are not your MS. You are a warrior, a survivor, and a person worthy of hope, love, and brighter days. 🙏❤️

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My knee hurts some tonight. Need a friend to talk too. My multiple sclerosis, in parkinson's and dementia. Is all acting up tonight? I wish I could say different, but it is what it is. I'm tough skinned how thick skin survivor of heart failure four times. I'm tough and i'm a soldier from the army, or at least I was in two thousand and one. I'll begin a new power wheelchair within the next 6 to 8 months. Hopefully, the one I have is starting to break down. Will you all say a prayer for me. I'd appreciate it. Nobody likes talk to me because I got so much going on..

Jurupa Valley, United States

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Edited

At heart Dr. Not doing good on may 16th my heart rate went to 153 not good. Plus I was diagnosed with dementia. My heart rate has been going up more frequently. Their probably going to do another ablation on my heart. Plus I was put on another infusion for my multiple sclerosis

Riverside, United States

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Heart related feeling and chest area feeling

For last week or so, i had a few mild single thuds in my chest (right side) different times of day, after beeing active or just resting, chest muscles have felt achy at points and some really mild cramp like feeling in between the ribs (not tied in with the Thuds they happen just at random) works be...

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My home away from home, if only in my head and heart.

One thing I do so love about my Video Games is they do not judge me for my MS and are always there, except during maintenance of course, and actually reward me for trying without ridicule or true expectations.

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Overdid it last week and had an elevated heart issue but also had my ocrevus infusion, since I am rubbish, shaking and cannot walk far, my existing symptoms are elevated, has anyone else experienced this

Swansea, United Kingdom

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Kaempferherzen - Fighting hearts

Anyone going to the Kaempferherzen meeting in Kassel Germany on 25th July? Seems like a privately organised full day. event for people with chronic illnesses including MS.

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Heat & High heart rate

Does anyone suffer from a high heart rate while in enclosed areas with heat and no ventilation? My heart rate usually goes up could reach up to 130/140 on my watch I feel nauseous and as if I will faint Is that only me or a common MS thing?

First posted on the Shift.ms app