My name is Lindsay and I was diagnosed in October 2014. Little did I know I had been dealing with MS issues for at least 13 years. What I put off to bad genetics was much more. At least I lived my fairytale for 30 years. I was super successful in my career, have 2 beautiful children, and an awesome, loving husband who has done his research because he knows more about the disease than I do. Lol I must say despite the constant shakiness, the fatigue, and pain... My life is pretty okay. I think I will write on here though. Sometimes I need to vent and I feel like a burden to my family so I'll vent on here. Have a fantabulous day everyone!
Do you have a fear of needles and take medication that requires injection?