New to shift..
But I’ve had my MS diagnosis for quite some time. Could use some support or just cool people to talk with. Right now my life is overtaken with MS this and MS that and I’m sick of it. If you don’t have it, you don’t understand it; so I’m hoping to find normal ms people surviving this encapsulating disease. Ones who know what it feels like to wake up and live with MS.
Hello and great you are here because that is exactly what made me want to check out Shift. My former boss told me it’s not MS it’s menopause before giving me the sack. My close family thinks I have Lyme disease or just want attention. I have been trying to figure it out for a long time but MS it is and it helps a lot to be part of this online community. So- hello! I have avoided normalness in many parts of my life but it’s normal to want friends, normal to want to be understood. MS can be incredibly isolating- so, at least here you may feel less alone in it.
Trust me with only being diagnosed a year and a year ago this the place to help me with all the support that is provided to us all