@gemstemple 

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gemstemple

MS buddy

Hi all Hope you all are having a day. I’m Gemma (34) I began have sympsons in spring 2013 but the doctor never seemed to put them all together so my offical diagnois of relapsing/remitting didn’t come till 2016. Im December 2017 a MS consultant said I was that the diseases had progressed to secondary. I don’t know anyone else with MS so I signed up to be matched as a buddy. I’ve had no response as of yet. I’m hoping someone on here will contact me and we can help and support each other. Thanks Gemma (Ps sorry for the ramble lol)
@miller

Hi i got diagnosed with ppms last year after a lot of tests iv had symptoms for many years just pleased i now know whats been going on lol

@Stumbler

Correct, @gemstemple , I think we're all "having a day"! :wink: It is beneficial to chat with other MSers, to share experiences, tips and tricks. The Buddy initiative is fairly new, so is still slowly getting going. But there are other options to prove that you're not alone. There is the Shift.MS Map, https://shift.ms/map , which plots member's locations worldwide (if they've divulged their locality). There are five members located in Basingstoke. There are also these couple of local gatherings :- MS Therapy Centre, Farnborough - http://www.mssupport.org.uk/ MS Society Basingstoke Branch - https://www.mssociety.org.uk/care-and-support/local-support/local-groups/basingstoke-district-group Although, you'll never be alone when posting on the forum..........