This Is MS Multiple Sclerosis Community: Knowledge & Support
Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
Hi everyone. I guess it's customary to post a short introduction so I'll try keep this brief.
My symptoms started in March 2010 with numbness and loss of coordination on the left side of my torso, the symptoms lasted only a couple weeks. An MRI showed information that pointed to MS however a lumbar puncture came back negative on all tests.
I had another brief flareup in July which I kept to myself but then things began to go rapidly downhill in November.
In late November I experienced severe numbness and loss of coordination in most of my body so underwent a further two MRI's which revealed several further lesions.
On Christmas Eve I experienced my first crippling flareup which rendered the right side of my body numb and my right leg almost useless. This flareup had almost receded when last Friday evening I experienced the scariest and most damaging attack so far.
The attack left me severely crippled and unable to walk, it also attacked my vision leaving me with a "vertigo" type inability to focus on anything. I have just spent four days in hospital where an intravenous drip of some hard-core steroid has corrected my vision and enabled me to get out of the wheelchair and stumble about like a marionette instead.
I am now back at home and waiting for my mobility to return slowly but surely. I have a consultation with my neurologist on Tuesday where we will discuss the best long-term treatment for multiple sclerosis. My neurologist had originally prescribed Copaxone but the hospital neurologist has suggested I need a stronger treatment due to the rapid evolution of my condition.
I've noticed that none of these introductions are particularly cheery and mine is no exception but I suppose like most newcomers I'm still pretty shook up, scared and looking for advice.
Without inadvertently breaking rules with product placement the only advice I can currently offer anyone suffering MS who needs to type as part of their job is to get a good speech recognition program (like the one I have used to compose this post).
Sorry to hear about your troubles. It's a really difficult time I'm sure. My advice would be to take a look at the CCSVI forum. It has worked very well for some people and it appears to work best with the newly diagnosed. http://www.thisisms.com/ftopict-12172.html Many people would disagree with me (your neurologist being one of them, more than likely.)
This site does not offer, or claim to offer, medical, legal, or professional advice.
All treatment decisions should always be made with the full knowledge of your physicians.
This is MS does not create, endorse, or republish any content.
All postings are the responsibility of the poster. All logos and trademarks in this site are property of their respective owners. All users must respect our rules for intellectual property rights.