well, at first I was over reacting to any word I get by my family. When I was first diagnosed they didnt even tell me I have MS I was so young even my doctor didnt tell me I was diagnosed in Saudi Arabia. But I was a wee detective I wrote my symptoms online and sussed it out and faced them and they hardly admited after getting my secong symptom. I asked is that cortisone again in my vien? they said no I said just admit it then they did. I lived kinda angry most of the time specially that I started interferon. then I went to University graduated in 2011. then in 2012 I hated my whole existance and I moved to the uk Scotland. I even met a guy hehe. shh ._. but I was kinda feeble lol and I was losing weight like crazy 38 kilos 155cm age 26 I volunteered part time job uk gov requirement to be allowed to study English. I did but it was lil bit stressful. but I assume changing the environment for a lil while helped me now I'm back to saudi everyone is understanding but yh they nag on me to find a job sometimes because I'm quiet well. or at least thats how I seem. meh my hand shakes a lil bit when I try to poor me a drink or milk out of a jar or something stairs stresses me I walk very careful and slow on them.

If you had RRMS when you were younger and now have progressive MS that means you have Secondary Progressive not primary. PPMS starts as PPMS. Keep strong and March on.

not quite sure what i have what im sure about is that i have atrophy in my brain by age 25 lol but suffer no disability at all. no symptoms but scary mri results that r getting worse

btw im now 28

+Nutshell AIC You are lucky if you have no symptoms, what a miracle. It is my symptoms that led to my diagnosis. I also have degenerative disk disease. Both are slowly taking my mobility away but it is the daily pain I struggle with the most. Keep strong.

I hope we all find a cure one day before its too late.