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![]() A newly-tested treatment for multiple sclerosis reduces relapse and deterioration in patients, without many of the negative side effects associated with other treatments, says a study. |
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Posted by:
limboland
Posted on: 09/03/2011 I am currently in limbo being tested for MS. I had a brain MRI in April that showed multiple [non-specific]white matter lesions in the sub cortical areas. I have a spinal MRI booked in October.
A bit of history:
In 2001, I woke up in the middle of the night tried to roll over and couldn't because my right side was numb. By morning I had some feeling and movement back but the side was still week and tingly. Dr ordered a CT scan and said there were no signs of stroke but definitly something neurological. It was left at that.
In 2006, I started getting a burning/ tingling feeling in the back of my legs. I had moved so I had a different dr he figured it was sciatica. This would come and go lasting anywhere from a few hours to a week at a time.
In 2009, I started having numbness in my toes. It went downhill from there. While camping one day I had a reaction to heat from the sun. My hands and feet started to feel like they were burning. We were at a lake and I had to go sit in the shade. Over the course of the day it got more intense and I started getting weird sensations in my arms electic type pains and even the feeling as if someone was flicking water on my arms. The pain continued to intensify and by the end of the day I could hardly bend my fingers. This lasted 3 days it hurt so bad I even slept on the floor with my hands over the air conditioner.
For the next four months I felt aweful. Weak, tired, could hardly walk up the stairs. Pain in my legs especially at night. Pain in my jaw/throaght, headaches, ears ringing,dizzy spells, numbness and tingling. the dr tested me for lupus twice, diabetes twice, porphiria and did like a hundred blood tests all came up negative.
I moved back to the town I lived in before a short while later. I felt great for about a year and a half then all of a sudden I started getting the leg pain again. I also started getting tingling and numbness and twitching in my face and eye. My feet and wrists started hurting and going numb, blurry vision in my eye never lasting more then a minute, chest pains, weakness, bladder issues and the scariest was when my legs went numb from the knees to my toes (lasted about 5 hours). It is to the point I had to stop working until they figure out whats going on and treat it.
My doc is unsure as to what further testing should be done. Any suggestions or advice is welcomed.
Posted by:
Adriana
Posted on: 10/08/2010 Hi Fisher, that is right, the warm or hot weather is affecting and worsening the disease. You have to protect yourself agains it. There are many other things what you ca do. My friend is a doctor, so if you want I can give you in details the informations you need.
Posted by:
Dale_Hormuth
Posted on: 08/19/2010 hi my name is dale hormuth i am 22 years old and was diegnosed with MS on may 29 of 2010 i have no clue how to deal with this so plz e mail me at acecoolcat@yahoo.com plz i would like to talk to someone about it |
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Posted by:
fisher(Guest)
Posted on: 06/01/2009 i am a suffer of m.s. when i am in the sun i start to dizzy and feel lighthead, i wat to know if the sun could make the disease worse or is it in my imagination.could anybody give me some advice thanks
Posted by:
guest
Posted on: 11/11/2009 My mom has ms and is very affected when she overheats. When outside she trys to stay cool by staying out of the sun. My understanding of ms is that the central nervous system is compromised, when we overheat and become dehydrated our central nervous system is affected. She exercises by swimming in a pool so she can stay cool. Hope this helps
Posted by:
wheelchairgranny
Posted on: 07/01/2010 HELLO, THERE ARE COOLING VESTS THAT WILL HELP BUT YOU NEED D3 - RIGHT NOW I AM ON 50,000 UNIT EACH WEEK. GET YOUR LWEVEL CHECKED AND STAY COOL ALSO ENTER RECIPES IN MY COOKBOOK I AM DOING WWW.TYPENSAVE.COM I CAN SEND YOU MORE INFO, SEND ME ADDY I HAVE PROGRESSIVE RELAPSING MS. |
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It is a disease for the whole life, but the treatments are not available, until you search in the right direction for it. It can be cured, as I know a few from them.