Hiya, I had an account here before, but have completely forgotten my old username (it's been a while), so I thought I'd rejoin.

I'm an active, dog lovin' Canadian girl. Been diagnosed 9 years. Love my life and all the fur that comes with it (I'm a dog trainer). I moderate a number of subreddits, including a small, relatively quiet one for MS (under this username). I'm on Avonex and am up for annual insurance ...

Hi All lovely MS people,

Thanks for letting me join, and i hope that you dont mind me spilling my problems out here! :) I also hope that some people searching for answers, like me too, might get help relating to some of my frustrations, and know you're not alone!!

Cant believe its been a year in March since the tingles started. Ive had 2 MRI's (one ...

Hi everyone this is my first post.
I have read a good deal on this site and others.

I have had a long hard go at this sudden change in everything and feel like an over washed shirt.
I turn to your experiences as a community.

After having a very sudden case of paralysis of the entire left side except torso I was told i had a sudden stroke and I would need to be ...

Firstly, let me have a chance to explain why i decided to join TIMS forum in the beginning. My main purpose was to contact dr. Sclafani and discussed about CCSVI with him. That’s it, i stated it in my earlier post in Introduction and my question was only about CCSVI.

Then someone replied, but not the answer i was expecting to get. I was excited though to have any kind of respond from someone else. ...

I've not yet been given a dx of MS, but I've sadly heard it from a handful of doctors over the past year, and am returning to the Neurologist to pursue further testing.

I'm completely overwhelmed, and not sure what to do at this point. The possibility of MS makes me so sad - I don't think I have it in me to fight this.

The suspicions started a year ago when I experienced a ...

Hello from Australia :)

OK, i'll try and make it quick. My mother got in contact with me recently to tell me that she had been told by neurologists that she most likely has MS. This is as the result of an MRI which showed lesions and an episode of numbness lasting 3 months, fatigue, an incident of feeling like she was walking on ice, plus noticeable ...

I am new to this forum also. I am a 35 YOA son to my mother who has very progressive MS for longer than I have been alive. I have posted a little something in the Friends and Family section about my mom too. I joined because I have quit a bit of knowledge of MS stages and pretty much the worst case scenarios as my mother has had pretty much everything. I don't know ...

Hello everyone

I decided to introduce myself here in this topic, please correct me if wrong.
My name is Leandro Silva Rogerio, I live in the southern region of Brazil, married with no children and am 34 years old. I have no motor problems.
Be discovered with multiple sclerosis after losing the palate, flavors not felt anything, sweet or salty, or bitter or pepper. Lived in search of something that could awaken my taste, not ...

I'm Leila and my beloved big sister has been diagnosed for 3 years now and it has been a roller coaster. She has a very aggressive progressive form and it has been the hardest thing I have ever had to deal with in my life. I always imagined we would remain close as adults, vacationing together, hiking together, running 5ks together, she would watch my babies while I worked since she stayed at home. I ...