I have RRMS

[Jesmcd2]

Have had it since 2015! 😯 March to be exact! Since then l have learned soooo much! And i sure didnt run out and buy depends! 🙂 I have learned to get knocked over and over again.. Get back up and know lm still good! 🙂

I learned that everyones MS is different! And no one should tell another how to live there best lives... Because sometimes if you listen, they are giving their best.... 🙂

Now, l might not have had this for oh idk? 780yrs?

But.. RRMS? Its not always bad! 🤣😂🤣 geeze

🤗💕🌠

[jimeka]

Well said Jes ,I think what you say also applies to PPMS, ms is what you make it, and there are no set rules. Just because one person declines quickly, it doesn’t mean we all do. Ms is a very individual disorder, no two people are the same. 👍

[Jesmcd2 CommunityAmbassador in reply to jimeka]

Very very true! Everyones MS is different! 🤗💕🌠

[falalalala]

Thanks for posting this.

I like your attitude very much and while I understand that having MS is not easy and people might want to talk to others about their struggles, I can't live in a state of dread and doom and gloom 24/7.

There is more to my life than MS.

[carolek572 CommunityAmbassador in reply to falalalala]

Yes, indeed there is, falalalala !

[Sandydemop]

Hey there Jes, live your best life no matter what, right?

[kycmary]

Any person who deals with a chronic disease is on an adventure that's the way I get through my life.

[Graip76]

I have PPMS and it is amazing how many people have crystal balls and know your future or feel compelled to tell you horror stories about someone they know. Thank you for your post. Everyone is different! My doctors have told me the same and for PPMS there is now a treatment that wasn’t available 6 years ago. The future should be encouraging not dreaded. Take care! Thank you again for a positive post 😊

[leking1]

Good Morning, Jes! I like your post! I used to have RRMS but I outgrew it and I now have SPMS. As you said, everybody is different, some people will do this, a lot will not. I don't know that is better or worse than the OTHER MS, it's just different. I like Falalala's attitude and I can identify with it. I've lived with this disease for 40+ years, and I can't start worrying about it now...it is something I deal with, it s Not who I am, and I have too much I want to do to waste my time ! So, do what you want to do, live your life the way YOU want to, and BE HAPPY! Linda

[twooldcrows]

well said ...we do will do what we can and can try harder on somethings if we think some things will help it ...i just keep pushing on and on thru thick and thin good and bad ...yes there are times after words i will have to stop and take some breathers but that is me for i will not stop till it takes me away for good ...i feel better after i have pushed myself but that is me ...all take care and be safe ....love and much happiness to all ...we live with it for nothing is there yet to stop it ...we just slow it down...

[kdali]

I'm here for the knock downs and the get back ups. There's all kinds of ways to do those!

[Cutefreckles72]

Thank you, Jes. I have PPMS and everyone is different. MS is painful mentally and physically. Keep pushing and Hang in there. Love my MS family. 🙏🏽👍

[BlanketTime1]

i'm glad you're so positive. we need that🤗.

[Jesmcd2 CommunityAmbassador in reply to BlanketTime1]

Dont get me wrong, we all know its not easy... And their are days l positivly hate it! 😡 but hate is a wasted energy... l have better things to do! 🤗💕🌠

[BlanketTime1 in reply to Jesmcd2]

🤗❤️

[carolek572 CommunityAmbassador]

C’est la vie, Jesmcd2 ! 🥰