@loulou 

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loulou

Feeling so alone with PPMS

Please tell me if there are any other PPMS'ers on Shift, I feel so alone sometimes as alot of posts seem to be for RRMS and DMD's, I am sure there are many others on here, I know our symtoms are all the same but alot of our drugs are not, I cant think of anyone else on here with PPMS, alot of the personal details just say "I have MS" including mine Pleeeeeese say hello if you can so we don't feel so alone and can talk to each other it would be so very helpful to us all xxx
@markms

hi how you i have ppms as well hope your ok x

@markms

hi sorry for the short reply at work and busy for a change lol yes i to have ppms how does it effect you you must be the first i have met with it hope your well? for ppms that is lol x