Hi julie,
i am a 25 yr old female. I have probably had mild symptoms of mulitple sclerosis all of my life. Mine has probably started since I was born. I was always told all of these different things by my neurologist like: traumatic brain injury, seizure disorder, vastibular bilateral integration disorder. I was always so confused as to what I had. I never knew I had the mild symptoms of ms. Right now I don't have full on ms, just mild symptoms. With me I have always had trouble with learning, some seizures;
i have problems remembering things, understanding, stuff like that. About a year ago I started going to a new neurologist, he did a consultation appointment. At my appt. My Dr. Asked me some questions. I had a hard time remembering, my coordination a little off. He had some idea about the mild ms; due to what he noticed at the Dr. Appointment, then he did an mri. The mri showed some stuff on my brain. So then my neurologist told me I have mild symptoms of ms.
For me I think as of right now I am about the only person I know of who has had mild ms all of my life.
With me sometimes I do really good, sometimes I can get worse, it all depends on if I am really relaxed & everything.
My neurologist told me if my symptoms get worse he wants to do a comparison mri to see if I have multiple sclerosis. But for now it's just mild symptoms of ms.
I am also pretty healthy as well: when I was in high school & junior college I ran track & cross country. I was extremely surprised & happy at how well I did. I did the best I could, I wasn't always the fastest one on my team. Everybody else was also happy & really surprised at how I did.
I am so sorry about your friend. What sort of things has he had to go through with his ms?
I'm not sure what to say to you really. I know that it can be really hard & sometimes really scary.
With me sometimes I get a little scared, because with me sometimes I am really great, then other times i'm not that great.
For me i've had to live with mine all my life, so I wasn't really surprised about it, just relieved to know what I have.
I can do everything I need to do, sometimes it can take a little bit longer for me, & I need a little more help.
Bonnie