shift.ms

Hiya everyone! Last weekend I had the opportunity to guest host the Twitter account for Shift.ms & it was a fantastic experience! I strongly urge others to look into it & give it a go sometime… #TwitterTakeover weekends are a great way to explore new topics, engage in conversation &a…

I am off balance a lot is there any chance of this slowing down

Hi ladies , I had cladribine in May and since September my periods are very irregular coming early 15 , 21 days ! I had a tummy scan and everything is normal, iron levels normal, thyroid is normal, confirmed i am not in menopause ……could it be due to cladribine ? Anybody experiencing th…

Hi I know its the worst memory in your lives probably I wanted to ask this question before but i didnt want to hurt your feelings and i still dont want that if cours But zi hope people with spms Tell me this year of daignose ehat age date of first physical permanent distinction You dont have to ans…

I have had nausea for months. I have lost so much weight and spend many days in bed. I have been to multiple dr. appts for this and have received no help at all. Dr. Google. I hate to admit it but what else can you do when you are desperate……….. So, I guess some people with…

I would like to reach out to others who have chosen not to take DMT. have you regretted this? And how long have you been diagnoised? I was diagnosed in 2007, chose not to start dmt and have been ok with this decision. After joining this group, i am realizing that i have had more ms issues then i th…

Hello I’m just new to this site hope to keep incontact with you all x

Hello Everyone, I live now in Co. Mayo. Was diagnosed with MS on my 40th Birthday 2006. My then neurologist & I discussed medication, decided on 20mg Copaxone daily injection. At that time I was crawling physically, suffering symptoms for six years previous I had no idea of what they were conne…

Hi everyone We have a local meet for anyone and everyone who wants to come. It is in the Showroom Cafe on 3rd Feb at 12.30 and we have the whole venue booked for ourselves. At the moment there is about 20 of us going, some people who are new to Shift, some who are new to MS and some old familiars.…

I’m new here. I was diagnosed in Feb 2018 and still trying to understand what my body is going through.