Be A Detective For A Night & Raise Funds For MS
Go back to the Roaring 20s. You're the Gumshoe racing to figure out whodunnit! May 30 at 3 pm PDT.
Match wits with other virtual investigators & raise funds for an important cause.
Benefits @mssociety ๐งก
https://t.co/lwEa3TpPqW
Living with Multiple Sclerosis means it's really important to remember self care and to set boundaries. Pamper yourself. Your body will thank you. ๐งก๐งก๐งก
@CarlaKCoach On Ocrevus since October 2017.
The Good: Completely stable. No new lesions since I began.๐๐พ
The Bad: Increased fatigue for months. Skin hurt on my whole body for 2-4 days. No hugs.๐ฅ
The Ugly: My hair fell out & broke off. Ran my fingers through and ๐ณ
Would I do it all again? ๐ฏ
Join Prof Maria Pia Sormani, Dr Susana Otero @cemcat_em and @PavanBhargavaMD on August 23 at 4:00 pm EST, 10:00 pm CET for the next @IntNatlWiMS Global Conference on #MSCOVID19. More info and Zoom link at: https://t.co/MQdhhZf5R9
For World MS Day we had fun on Virtual Murder Mystery Night For MS ๐งก
Chef thought he would get away with it if it wasn't for those meddling MS Warriors & Allies!
Next year will be even better. Proceeds benefit @mssociety#MSConnections#WorldMSDay#MSDiva#FightForACureForMS
Costs of living are growing, but wages are stagnant. No one should have to choose between paying for health care or rent & other necessities. @AdamGrayCA we need an Office of Health Care Affordability to address rising costs. Please vote #YesonAB1130 by @JimWoodAD2 #MSActivist
@TheDianeKramer @mssociety How exciting. I'm so happy for you. You will indubitably be an asset to the Board and the Society as a whole. Hopefully I'll see you on some of the Leadership Volunteer Calls. So awesome!!! ๐งก๐งก๐งก
If you or a family member are living with MS, please complete the Economic Impact of MS Survey. The results will be used in discussions with policymakers to advocate for policies to improve the lives of people with MS. https://t.co/E3YwpE4NGT #MSWarrior#MSActivist#MSDiva