new on the site....

[yeb4432]

hello everyone, i am new here. i have hadms for nearly fifteen years and have been on every approved ms med, save novantrone. ironically enough i am also a physician's assisstant in a neurology office. i rarely share with my patients that i too have ms, but have started to more recently, especially when it is relevant. i still stuggle with when to share and when not to share this information. i would love and appreciate other's feedback on this.

i am also very interested in medications in the pipeline. currently i am on tysabri, almost two years now. by far the best med i have been on. as interested as i am in the pipeline meds as a patient with a fairly advanced ms, i would never risk additional progression on untested meds, especially with meds that are currently so effective. imho

i would love other people's feedback on the patient provider ms thing though...