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Getting older with MS
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Courtney_J
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Courtney_J
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Last activity on 08/08/2022 at 11:09 AM
Joined in 2020
1,340 comments posted | 96 in the Living with Multiple Sclerosis group
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Hi @MS_283, thank you for opening this discussion! Let me tag some other members who can possibly share with you.
Hi everyone, how are you today? Have any of you heard about how MS can change as we age? Have any of you noticed your MS evolving as you've gotten older? Has it gotten worse? Better?
@ArturK @vonstar28 @MSlupuswarrior @JuliePlave @tinawest9877 @JennaGreen @Karen9905 @Nicki21 @Dselle00 @HrlyBabe4 @paulakasson @Scotlind99 @Onlymwilliams @KylanP @Gotwle @Ldough @Ndinda @Masseryp
Feel free to share here!
Take care,
Courtney
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Courtney_J, Community Manager, Carenity US
paulakasson
paulakasson
Last activity on 06/14/2024 at 2:35 PM
Joined in 2021
7 comments posted | 2 in the Living with Multiple Sclerosis group
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Yes, it has gotten worse, especially my memory!
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Paula James
cmadsen99
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cmadsen99
Last activity on 09/06/2021 at 7:46 PM
Joined in 2020
20 comments posted | 2 in the Living with Multiple Sclerosis group
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Actually, at sixty-one I stopped taking my Betaseron because a seventy-year-old lady I met on a cruise told me after 60 the medicine didn't do much good anymore. I was glad to hear that because I was so sick of giving myself shots every day. I am now sixty-nine and I have had no relapses. I will admit a twinge or two but I also got the with the medicine, but I still keep to all the other things I was doing for my MS.
I had the two Covid shots and I was fine no reactions.
DebraBeyer
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DebraBeyer
Last activity on 10/31/2024 at 11:28 PM
Joined in 2020
19 comments posted | 6 in the Living with Multiple Sclerosis group
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Dx at 64,now 66 with PPMS. Miss all those great years I had bc this disease stinks. Ready for new challenge as I was bored being newly retired and can no longer golf,drive my car etc.
phyllis
phyllis
Last activity on 12/10/2021 at 1:41 AM
Joined in 2020
4 comments posted | 3 in the Living with Multiple Sclerosis group
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I am 83 and have been with this for over half my life. I was getting slower at things at first, but as I grew older I lost the use of my legs. I feel completely useless. I have lost all my good friends, volunteering, and keeping in touch and isolated myself from the rest of the world,
Twig57
Twig57
Last activity on 09/21/2022 at 11:58 AM
Joined in 2021
3 comments posted | 3 in the Living with Multiple Sclerosis group
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I’m 64, diagnosed over 30 years ago, and no longer taking disease modifying drugs. Unfortunately, the Secondary MS symptoms have continued to worsen. Scary and discouraging
MyMS55
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MyMS55
Last activity on 11/18/2024 at 1:12 AM
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60 comments posted | 21 in the Living with Multiple Sclerosis group
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I have had MS diagnosed 36 years but my first flare was 40 years ago. I'm 55 I'll be 56 in November. Started out with RMS have run the gamut on the medication. Now on my second biologic drug and I've been diagnosed now with active secondary progressive by my new neurologist. I'm slowing down unable to drive anymore. Still walk with a tall Walker and have an electric wheelchair for when I go out around town. I could look at all the things that I've lost and be sad but I look at all the things ahead the challenges are like an adventure to me. That in my relationship with the Lord keeps me going each and every day.
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Melissa Vemi
jannie45
jannie45
Last activity on 02/21/2022 at 6:06 AM
Joined in 2022
4 comments posted | 1 in the Living with Multiple Sclerosis group
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@MyMS55
Oh I am feeling sorry to hear about your health. May God bless you with health.
After surgery, I used [link removed for violation of community standards] tall walker. I was a bit hesitant. I decided to give it a try. It was not fit for me because of my height and weight. Always Stand with your shoulders relaxed and your arms hanging loosely at your sides. The walker height should be at the crease of your wrist when your arm is extended.
MyMS55
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MyMS55
Last activity on 11/18/2024 at 1:12 AM
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60 comments posted | 21 in the Living with Multiple Sclerosis group
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I'm finding the tall Walker is very useful for me. But right now I'm waiting for a custom built electric wheelchair to replace my jazzy which makes me look like I'm riding in a child's electric wheelchair. It only comes up to the bottom of my shoulder blades so my whole upper arms and shoulders have no support. This new Walker will be very supportive and a lot better alternative.
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Melissa Vemi
ColeenCoon
ColeenCoon
Last activity on 06/23/2022 at 12:35 AM
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2 comments posted | 2 in the Living with Multiple Sclerosis group
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@MS_283 I am 55 I have had Ms since my teens. My MS hasn't gotten better. It depends on your medication and your Neurologist staying on top of it. @MS_283 @MS_283
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MS_283
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MS_283
Last activity on 11/23/2022 at 9:27 AM
Joined in 2018
57 comments posted | 36 in the Living with Multiple Sclerosis group
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Hi,
I've had MS for 10 years now (diagnosed in my early 30s), and I'd heard that after 55-60 MS stops being as progressive... What does that mean exactly? Does that mean it'll get better at that age? If I know that it'll eventually get better I'll be glad to have something to look forward to!
Thanks for any replies!