So, I suppose I'm officially not a Limbolander anymore. I saw my neuro yesterday, and due to there being a single lesion on my spine (none on the brain) and my having had two attacks, he diagnosed me with RRMS. This sucks, obviously, but I am hopeful. He said that due to the relative mildness of my symptoms, and the nature of them (On and loss of temperature sensation in left leg, two and a half years apart) chances are good that I'll experience a milder case, especially on medication.
I'm still switching some between freaking out and being relatively calm about it. I suppose I just have to live my life as if I have mild MS, and then if things change, I'll adjust then.
Neuro also said that it is rare for people to get ON in both eyes, and that many people do not get recurrent ON. This, along with the hope that I can continue to move a pen is important to me, as I work as an illustrator. Either way, here I am, on team MS. A little sad about it, but I can't change my DX. I just hope to get to live a somewhat normal life.
I'm still switching some between freaking out and being relatively calm about it. I suppose I just have to live my life as if I have mild MS, and then if things change, I'll adjust then.
Neuro also said that it is rare for people to get ON in both eyes, and that many people do not get recurrent ON. This, along with the hope that I can continue to move a pen is important to me, as I work as an illustrator. Either way, here I am, on team MS. A little sad about it, but I can't change my DX. I just hope to get to live a somewhat normal life.
Comment