It all started when I was a sophmore in high school. It begain with numbness and tingling all down my right side. It became so bad that my right side of my face was drooping, I had problems with numbness off and on for 5 years. Then when i decided to move away to college and I worked a full time job, the numbness, headaches, and brain fog became worse. I was finally put in the hospital after 5 months of that. I had to drop out of school once I was let out of the hospital, they would not let me make up my finals. So I moved back home and the confusion and tingling are not any better.

Please do not wait on going to a doctor, if you are like me, and think it will just get better, IT WON'T!  If anything, your disease will get worse.  As of right now, I am really not sure if the Beta Seron is making the disease better, I'm afraid there that activity in the my brain is increasing with all of the numbness and excruciating headaches that I have been experiencing lately.  I must say that I am still estatic to be alive and just knowing that people out there in the world have it ALOT worse than I do, it keeps me going and gives me tons of hope that one day I might be normal again!

I must say that since I have been on ProKarin that my symptoms have gotten a lot better.  Even though I still have the headaches they are simply stress headaches because I do not do well with stress.  I have to recommend to read Elaine DeLack's book "They Said It Didn't Make 'Cents'".  It really has a lot of facts why MS is NOT auto-immune and I truly believe that!  Just for the record.......lol.