Tricia's Story of Multiple Sclerosis
Uploader Comments (MSPacific)
Top Comments
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I got ms and i got 30 lesions, am 20 and they say its miracle i even walk, i say fuck em fuck all doctors coz they dont know shit, they tell u all the worst stuff ms can do to u and then they say there is no cure and u cant fight it, well blow me am not giving up on this shit
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All Comments (126)
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Dear Beloved Tricia,
you are such a beautiful mom~warrior and soul. I look to you for inspiration.... I v'e had MS since the early 80's but it didn't stop me but for short periods . too busy ! Now I'm 48, married with 3 teens going in 40 directions
.3 different schools & I couldn't be prouder of them. meanwhile, mama is in bed with trigeminal neuralgia! FUN FUN! half- blind with shingles in left cornea (all ms related) when I am better, must volunteer -
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I am 48 and have had MS for 15 years.
MS 'behaves' in many ways
I began with optic neuritis, but this has never recurred & my sight is good.
I can still do most things with adaptations!! I can walk, not very far and sometimes with a stick, but I can! I wobble sometimes, but focus on something ahead & stay straight! I have to rush to the loo, but now take medication which helps. I get tired, but pace myself and rest.
I worry about my kids and the future, but I
stay positive most of the time .
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Thank Tricia, your video is helping me to know more about MS. My fiancee just diagnosed having MS and I need all the input for us to go through our life with MS...
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I have recently been diagnosed. I am also a single mom..my first attack was optic neuritis of the left eye as well. Thank you for being brave enough to make a video. You have helped me today. Love and Light to everyone who suffers from this disease, their families, and their friends.
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"i'd walk forever for you mom" - what an incredible gift God has given you in your son... keep the faith
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I've had MS for 4 years. I was 30 at the time, 34 now. I realize how many things there are that I can't do now, that I could do even 2 years ago. And there are still things that I can do now that may become impossible by next year.
I won't say that I'm "happy" to see other people with the same problems (or worse), but I am comforted to know that I am not alone.
Alastair Farrugia
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It amazes me how unselfish people become when you are hit with this disease,
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Thanks for sharing Tricia. MSPracif posted the vid so I assume also has MS. I think that science will some day find an answer for us. For now, all we can do is our best to live a fulfilling life and take the therapies that are available. I bought a 400 cc scooter myself and it was very therapeutic. Take your B vitamins to help with the energy, and don't overstretch yourself.
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hola tricia mi nombre es Noelle soy española, y me detectaron EM a los 26 años a los dos meses de casarme con el hombre que me haria la mas feliz del mundo, y quiero decirte que tu video me da fuerza, soy feliz tengo muchas ganas de vivir, y tu me has regalado una sonrisa en mi cara, no te conozco pero me alegro de haberte encontrado, te mando besos y decirte que me has ayudado. besos y gracias.
9/25/08
Thanks for the kind and encouraging words!
Jake will be 15 this year. He is a high school freshman and still loves playing baseball. He raises money and awareness for Walk MS and this year he's riding in Bike MS. He is my inspiration!
I have good and bad days, but am blessed with supportive family, friends and doctors. I fight for a cure through volunteerism and fundraising. I know I speak for many when I say I want to live in a world free of MS.
With Hope & Love,
Tricia Chandler
MSPacific 3 years ago 16