This Is MS Multiple Sclerosis Community: Knowledge & Support

I suppose that I have graduated from this sub-forum.

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Every year without knowing it I have passed the day
When the last fires will wave to me
And the silence will set out
Tireless traveler
Like the beam of a lightless star

Then I will no longer
Find myself in life as in a strange garment
Surprised at the earth
And the love of one woman
And the shamelessness of men
As today writing ...

I was diagnosed a year ago after having a seizure in my dorm room and waking up blind at age 18. Since then, I've had botched spinal taps, bad drug reactions and little hope. Luckily, I changed doctors and am now feeling better than ever. I've taken my experiences and started a blog, especially for women with MS, in which I discuss medications, healthy recipes, MS friendly exercise and more. Here's the link for anyone ...

Diagnosed less than a month ago. Since then I have tried taking to "intensive nutrition" and Vitamin D supplements. Working on improving that regimen all the time.
Anyway, a little about my sitch: I'm a full time college student from the PNW about to turn 22. First symptom, some tingling and numbness in right foot, stiff knees. Leading to diagnosis-nystagmus.
Right now I am in the middle of an exacerbation. Steroids got rid of the ...

Lately, I've noticed my legs have been jumpy and twitchy. I googled it out of boredom, and when ms came up, I was drawn to it because my aunt has it. I've experienced blurred vision. I used to have phenomenal vision. Now I can't read things I used to be able to. It comes and goes. I'm always exhausted. Even if I get twelve hours of sleep, I'll come home from school and fall asleep ...

Since being diagnosed with ms a lot of things have changed for me. my habits, exercise, diet, everything.

There's only one thing that hasn't changed at all.

I like girls. Iv'e always liked them, always will. Im 21 so im trying to meet and talk to as many women as i can.

So when do i tell them about my little problem? I think im good looking, cool and funny. I have no problem meeting ...

Finally found a forum which won't get closed. I had been on other forum of ms, thought that i'll stay permanent on that site, but the domain was one day put on sale.
I'am male 21 yrs. Got ms diagnosed when i was 18, specifically 17th July, 2009. I had several symptoms of MS at that time, ranging from numbness, tingling sensation, severe optic neuritis, balance problem, heat intolerance, vertigo, swallowing prob. and an unusual ...

So in mid October I was at work and started feeling off, as the day went on I noticed my handwriting was off, by the next morning I felt like my leg was super heavy so I took the day off from work. The day after when I woke up my gait was off and my hip down was numb, was referred to a neurologist who got me a ct scan. That came back clear, ...

Hi,
My name is Amber.
I was recently hospitalized due to my body from the neck down going numb, and since this was not the first time I'd had numbness they did alot of tests.

They are fairly sure I have MS, but I cannot be officially diagnosed until I get into the MS clinic, and my appointment there isn't until late October.

I've been experiencing a myriad of symptoms and each one scares me ...

So I am curious, how many people out there have got into a relationship after their diagnosis that has been so far successful? I wonder because my first exacerbation was somewhat responsible for the ending of my last relationship and now I find myself wondering every now and then if I will ever meet someone who will accept me with my disease and I wonder if anyone should even have to deal with this but ...

sorry to type a topic so blue
but im 19 years old, had life ahead of me, now ill be lucky to be 50.
don't see the point in dating, school, anything really

im sure some of you had these thoughts when you first got diagnosed
but i really would like to hear how you got through these times

this is terrible, my initial symptom was optic nueritis making my eyes hurt and colors wierd ...