im sorry for your condition. i have no idea the suffering you are going thru. i think your a smart girl and this is a shitty thing to happen to such a beautiful girl. i wish you and your family the best. merry christmas.
hola soy javi desde españa y tengo mielitis espinal, me kede con 22 años en una cama ahora tengo 27 y hago casi una vida normal pero amo el deporte y la competicion quiero recuperar mis marcas, pero los medicos me dicen que no puedo ni si quierea se preocupan por mi El problema es que me siento culpable por lo que me paso y aun no me he perdonado, cada vez que hago pruebas fisicas lloro, por peder todo mi potencial, que hago? me rindo ? donde puedo encontrar ayuda? siento mucho tu dolor lo compa
I am 15 years older than you, but i know what pain you are in, I broke my neck in 1987 and still cant get ppl to get close to me. I wish you better luck than I had. I know what you want and what you are missing. being close to your loved ones is as much I can hope for.
Ba, I know what your going thought for I suffer from TM myself I was struck in 2005 and not knowing what it was my Doctors had no control over it .This year I lost my Nero. Dr. and was sent to another one I thought I was screwed and it was a blessing for he Knew just what it was I had he ran more test and it was confermed TM but not knowing all these years took a toll and all most killed me twice with the last time causing my lungs to stop. It Sucks I know !!!
CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Hi...How are you doing tonight? I am so sorry for you!! How are you doing these days? After your Ketamine Infusion. I am here to listen, if you care to talk! It is sites like this that makes people that are inflicted with the same disease, we can go to our computers and a couple of clicks and there we are connected to the world. I really do hope that you are doing much better. Keep Smilin' Lynn
I been through this myself it took me close to a year to become 100% better. I had a bunch of MRIsto check for any brain lesions and spinal taps to check the fluid for rings and plaque. so far my brain looks good and healthy. TM has the same symptoms as MS. but you only have 1 spot on the cord with no progression. Best of luck i hope you get better.
i was diagnosed july 2006 and i was depressed at first but then a little girl in the room next to me in ICU died. then i relized he it could be worse. yeah i know its sucky but you cant live life sad and depressed. dont dwell on what you dont have. look at what you do have and ask your self do i really have it that bad? because you dont your alive and here on this earth.
I feel your pain and I so wish I could do something to help! I don't have TM, I have MS and while it's different, it's also quite similar and I can understand what you are saying. During my relapses, I wanted to be alone too and I prefered to be alone. Now that I feel better, I am almost back to the person that I was.
I do go to Hopkins to get my care and I know about Dr. Kerr and yes, he is a wonderful person.
i know what your going through, i have it too. I got it when i was in 4th grade and im still dealing with it right now. I just have to pray tho it is frustrating at most times for me
I have had 2 attacks of transverse myelitis and i am here to bring EVERYONE OF YOU INCLUDING THE GIRL IN THE VIDEO MOSTLY hope! I made a full recovery but not til after 2 years of intense therapy there is a gentleman at John's Hopkins Hospital in Baltimore named Douglas Kerr. He is the director wordwide for the transverse myelitis center. I guarantee he can help you guys he did me and he did thousands of others. Keep the positivity, when you think down you feel down.
My name is Sue Dingle I was diagnosed in July 2008 I have a lesion across my spinal cord at T6-T7. You are welcome to contact me on facebook my e-mail address is on there as well. I wish I could say everything is going to be okay but I can't, but things have got better with time. I don't think I could be as physically and mentally well as I am now without swimming, kids and staying in Uni, mentally I find strenght in being busy. I hope you find your way to.
im sorry for your condition. i have no idea the suffering you are going thru. i think your a smart girl and this is a shitty thing to happen to such a beautiful girl. i wish you and your family the best. merry christmas.
SCARBAND 3 months ago
hola soy javi desde españa y tengo mielitis espinal, me kede con 22 años en una cama ahora tengo 27 y hago casi una vida normal pero amo el deporte y la competicion quiero recuperar mis marcas, pero los medicos me dicen que no puedo ni si quierea se preocupan por mi El problema es que me siento culpable por lo que me paso y aun no me he perdonado, cada vez que hago pruebas fisicas lloro, por peder todo mi potencial, que hago? me rindo ? donde puedo encontrar ayuda? siento mucho tu dolor lo compa
librehidalgo33 4 months ago
I am 15 years older than you, but i know what pain you are in, I broke my neck in 1987 and still cant get ppl to get close to me. I wish you better luck than I had. I know what you want and what you are missing. being close to your loved ones is as much I can hope for.
Shrpdrt 7 months ago
Ba, I know what your going thought for I suffer from TM myself I was struck in 2005 and not knowing what it was my Doctors had no control over it .This year I lost my Nero. Dr. and was sent to another one I thought I was screwed and it was a blessing for he Knew just what it was I had he ran more test and it was confermed TM but not knowing all these years took a toll and all most killed me twice with the last time causing my lungs to stop. It Sucks I know !!!
ke5glb 7 months ago
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CCSVI Clinic Receives Joint IRB Approval for Aftercare Protocol Study.
The joint application between Noble Hospital and CCSVI Clinic has been approved through the IEC Institutional Review Board (IRB) that will allow researchers to use patient data to study their new extended and enhanced aftercare treatment protocol. Please Call 888-419-6855 to know more about participating in the study. Log on to ccsviclinic. ca for more information. Email apply -at- ccsviclinic. ca
Gregmills007 1 year ago
Hi...How are you doing tonight? I am so sorry for you!! How are you doing these days? After your Ketamine Infusion. I am here to listen, if you care to talk! It is sites like this that makes people that are inflicted with the same disease, we can go to our computers and a couple of clicks and there we are connected to the world. I really do hope that you are doing much better. Keep Smilin' Lynn
RSDvlog 1 year ago
I was diagnosed with TM last year and I know how it feels. Be strong...
Tnkr90 1 year ago 3
try cannabis its great for neurological pain and depression, my brother is in a wheelchair and swears by it.
newworldodour 2 years ago 4
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I been through this myself it took me close to a year to become 100% better. I had a bunch of MRIsto check for any brain lesions and spinal taps to check the fluid for rings and plaque. so far my brain looks good and healthy. TM has the same symptoms as MS. but you only have 1 spot on the cord with no progression. Best of luck i hope you get better.
umlqqknatu 2 years ago
i was diagnosed july 2006 and i was depressed at first but then a little girl in the room next to me in ICU died. then i relized he it could be worse. yeah i know its sucky but you cant live life sad and depressed. dont dwell on what you dont have. look at what you do have and ask your self do i really have it that bad? because you dont your alive and here on this earth.
93MNP 2 years ago
Oh, sweet Melanie,
I feel your pain and I so wish I could do something to help! I don't have TM, I have MS and while it's different, it's also quite similar and I can understand what you are saying. During my relapses, I wanted to be alone too and I prefered to be alone. Now that I feel better, I am almost back to the person that I was.
I do go to Hopkins to get my care and I know about Dr. Kerr and yes, he is a wonderful person.
I hope you are feeling better now.
Many hugs,
Angela
angelusa73 2 years ago 4
I was just diagnosed in the April 09. I'm completely paralyzed. I know what are you are going through.
paule720 2 years ago
How are you doing now, NeuroDetour?
CarramelApple 2 years ago
i know what your going through, i have it too. I got it when i was in 4th grade and im still dealing with it right now. I just have to pray tho it is frustrating at most times for me
Andrea1046 2 years ago
I have had 2 attacks of transverse myelitis and i am here to bring EVERYONE OF YOU INCLUDING THE GIRL IN THE VIDEO MOSTLY hope! I made a full recovery but not til after 2 years of intense therapy there is a gentleman at John's Hopkins Hospital in Baltimore named Douglas Kerr. He is the director wordwide for the transverse myelitis center. I guarantee he can help you guys he did me and he did thousands of others. Keep the positivity, when you think down you feel down.
myrical1 2 years ago 2
I'm so sorry to hear about what you're all going through, my thoughts and prayers will be with you.
WhiteLionness 3 years ago 4
Hi,
My name is Sue Dingle I was diagnosed in July 2008 I have a lesion across my spinal cord at T6-T7. You are welcome to contact me on facebook my e-mail address is on there as well. I wish I could say everything is going to be okay but I can't, but things have got better with time. I don't think I could be as physically and mentally well as I am now without swimming, kids and staying in Uni, mentally I find strenght in being busy. I hope you find your way to.
Many regards
Sue
duchessjewell 3 years ago