I have be dx in1986 w/ RRMS, I had be misdiagnosed approximately 5 times, one of the Dr.s telling me to quit my job in a jail because I was a woman.
Long story short I went completely paralyzed and in a rehab for approximately 6 weeks. I learned to walk, talk, adl, etc until my
release when I went to outpatient Pt, and finally back to work on light duty.
Zoom to 2023, I have a loving genius of a Neurologist for 32 yrs. I am on Tysabri going on 13 years and am doing very well physically right now. I have some Cognitive Quirks. But am lucky that all I have no problem with physical mobility.
I retired from 13 years on my job quite awhile ago, and had to fight for my SSDI, but finally got it.
I am here to offer support for any questions you may have.
Please be wonderful and happy!
Marci
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BlondiePink
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Welcome to this forum, BlondiePink . You have a lot of life experience and you are willing to share this with others. That’s wonderful because we all have shared and unique experiences. We can all benefit from these and this forum is a great place for that. I look forward to hearing more from you. You can go to mymsaa.org for everything ‘ms’ related. Keep Smiling!
Welcome Marcilew, glad you're doing better and the victory with your SS benefits. We are here for you as well! A community of kindness and support. Peace and Blessings. NeeC
Hi BlondiePink Welcome to the family! We are all here to help eachother get through MS together! The good the bad the happy and the sad! Take a look around and jump in anywhere! (Using your email isnt recommended) 🤗💕🌠
Thanks so much! This seems to be a very warm place and I have been jumping around all over for a few nights now. I really like it here. Everyone is very welcoming and kind.
I hope you find being part of this forum worthwhile. However, a word of warning - places like this one have lots of nice people on them, but they are also are just another trawling ground for various scammers and other not-so-nice people so if you can edit your post to remove your e-mail address it would be a very wise move to do so. E-mail addresses can be hacked and hijacked and used for devious purposes so it's a really bad idea to share your personal e-mail address with thousands of people you don't know - and while many people join a forum like this and rarely visit it, you have disclosed your private e-mail address to more than 8,500 people you don't know.
If people on the forum want to contact you they can always do so through the private messages function which is part of this website's software program, and you can interact with other members that way as well. Sorry to sound like an old stick-in-the-mud-party-pooper, but in these days of hackers and scammers you have to be super careful about giving out any private information.
In the second last line of your post you wrote "Do not hesitate to email me at ......@xyz.com."
There will be a "button" under the post which says "More" and has little down arrow next to it - if you click the arrow it should give you the option to "Edit" your post. When you click on "Edit" you will be able to amend your post. When you have made the changes you want use the blue button down in the right hand corner which says "Post", and when you click on this the post will be saved with your changes made.
I worked for another 18 years, retired, then worked another 7 with my husband. 😳 I have annoying symptoms, fatigue issues, some cognitive issues. Still strength training, walking and gardening. I am very fortunate. Glad you are doing well too!
I am walking unassisted, but can’t run. I go for Balance Therapy weekly and love my PT as well. I’m so lucky to have a great care team!
I definitely have cognitive issues, especially my memory. But Neuro swears that it’s stress and not MS. I’m having multiple issues with my elderly parents and am having a hard time dealing with it!
You too! BTW, I can't run either. My legs would get super heavy very quickly. Stress definitely affects my brain in crazy ways. I have had some really, in hindsight, hilarious things happen when my brain "locks up". Best of luck with your parent's situation. It can be so darn hard.
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Best way to get disability 
Been a while!
Living & Loving Life the best I can
Life after MS is definitely possible!
