Post 598 It is getting closer 12 ... - My MSAA Community

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Post 598 It is getting closer 12 Feb 2020

RoyceNewton profile image
4 Replies

Good Morning my ms Sisters and brothers. We or more correctly I am closing in on Post 600. Do I continue beyond this? What is your opinion, just PM me a yes or a no. I may pay attention I may not. It just depends upon the day.

I understand that not all of our family speak the Queens English as a first language so if “YOU” do not, please PM(Personal Message) me and feel free to ask for a longer explanation.. With that in mind a young lady asked about exercise I think we should talk about this. I understand that exercise to a lot of people is a dirty word. I would say make it your friend, do it learn to enjoy it. Move your body while you can. Keep joints limber muscles active. I get great enjoyment walking into the gym and staggering out after a workout. I have warned the staff and I have a bright red wrist band saying I have ms just in case something goes wrong. It also makes it a lot easier to ask for help or advice.

Working out is also good for social interaction. There are several older gentleman in my gym who always say hello and I am sure I could ask for help if I needed it. There are several younger women that have very well developed glutes (back ends) that are always willing to give advice on how to develop mine. Get your mind out of the gutter ms Sister. Glutes are an important part of the core (Your middle) and a strong middle is important to us. Get out of bed, stand up straight and “YOU” will realize how important your core is. I do not like running, nor can I do it anymore so that is easily avoided. If “YOU” can keep yourself cool, do itl. By now everyone should have gone to Amazon and bought body charts and have them on the walls around your house. “YOU” know that if “YOU” use a muscle group a lot, it will warm up. Warm blood in your Central Nervous System (CNS) causes ms difficulties, and we do not want that. Do not exercise alone, keep yourself cool. Stand under a fan, wear a cooling vest, ankle or wrist straps, a cooling scarf or if “YOU” are really trendy a cooling head scarf.

There is no need to give up everything, merely because “YOU” have ms, in some form. Think about what “YOU” want to achieve. Ways that “YOU” can approach that goal, then go for it. “YOU” and I have Relapsing-Remitting ms (RRms), That is no reason for us ever to give up on our dreams, modify them YES, give up NEVER. Ignore the naysayers make a GREAT RRms life your truth.

Royce (the ms writer)

I still want to go into space, how, I do not know YET

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RoyceNewton profile image
RoyceNewton
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4 Replies
DM0329 profile image
DM0329

You must continue! Your posts drew me out of the shadows as a lurker here (which is funny due to my long-standing MS dx) you'd think as an MS warrior I'd be less shy! MS=Mighty Strong! :)

FWIW, everyone here is great. Folks who responded to my Social Isolation post helped me, too. For once, I'm now "excited" about my Medicare status (getting my "Silver Sneakers" card mailed to me as I type LOL).

My treadmill at home is great, but as I'm now 52 (ouch!) I think I need more than just cardio. As MS progresses, I must get stronger! I'm using my Silver Sneakers card to get "FREE" workouts and strength training at my local gym! So, I kill both the "isolation" and "weakness" together!

For folks who are in the chilly Northeast with me, Spring is right around the corner, too! :)

gotcha401 profile image
gotcha401

I do not know how to p.m. (social media challenged LOL) so I'll just reply here.. YES please continue if you can. I'm the newbie that reached out to you earlier this week. I truly enjoy your posts and have learned so much from you already. You are so very inspiring and keep my hope up. Sincerely, Hope (my real name) a.k.a. gotcha401

twooldcrows profile image
twooldcrows

now this is truly up to you but i myself really enjoy reading your writings for the help with MS and other funnies that have happened so we all don't think it is just us ...you have inspired me to much that yes we have a disease but we can and will still have a life that is our own personal journey that we go at our own pace....yes we can and i will not let it stop me until there isn't anything left in my mind and body to move ...thank you very much for all of the helpful to go on that we can with working with what we have ....find a way ,another way if can't the way before.....well i don't know what else to say but you have been very helpful ...love and much happiness ...if you want to go on to do more for your self and special lady to have some more fun do it....

carolek572 profile image
carolek572CommunityAmbassador

Well said, Royce. Just move because it makes you feel better afterwards! And keep on posting, my friend because you inspire me to just do it (whatever 'it' is) in spite of 'ms' :-D

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