Two best friends whose mothers both have MS. Together we have created a Walk MS Team with the National MS Society to raise funds, awareness & help find a cure!
ALT 🧡 Check out our story! https://www.instagram.com/p/CY33Jo0Nx26/
👣 Follow us on Instagram:
http://instagram.com/usvsms
👍🏽 Like/Follow us on Facebook:
http://facebook.com/usvsms
🔗 Donate to our WalkMS team:
https://mssociety.donordrive.com/participant/teamusvsms
✍🏽 Share your story and experiences with us:
https://forms.gle/FGWeKoEJ6ofrcCdd7
Join Dr. Jacqueline Rosenthal and Victoria Marie Reese for part one of MSAA's New Directions 2022 Webinar Series: Living with MS as a Black Person Participating in Clinical Trials: Your Opportunity to Make a Difference.
To register, visit: us02web.zoom.us/webinar/regi…
🚨 Attention all #beachlovers, we had added 22 NEW locations! ☀️🏖️🩱🩳♿
🗺️ This is a map listing various #beaches with wheelchair-accessible pathways.
🔗 To access the Accessible Beach Pathways Map use this link: google.com/maps/d/u/2/edit?m… or, click the link in the bio!
ALT https://www.google.com/maps/d/u/2/edit?mid=1IuZjpH903x7WDdnoUct1IHn-fxZwWFGX&usp=sharing
Hey teammates 👋🏽, did you know we are on Facebook and Instagram? Are you connected with us? Look us up and check us out @usvsms, see you all there we’ll be waiting❗🧡😊
Facebook: facebook.com/usvsms
Instagram: instagram.com/usvsms#usvsms#curems
Many family members and friends of someone with #MS may find that they are taking on some aspect of #care.
This may include personal care, help with day to day tasks or helping someone get around.
Find out about #caring and some of the support available:
mstrust.org.uk/life-ms/famil…
Disparities in healthcare — diagnosis, treatment & access — are among the top issues that affect people of color. Antoinette, Robin and Lawaunda, three Black women with multiple sclerosis, offer their personal insights about healthcare. #BlackMSExperiencentlms.org/BlackWomanWithMSSp…
The Black MS Experience Summit is coming up in just a couple of weeks! Join us June 15-16, for a safe space to share in the challenges of living with MS, from diagnosis and treatment to long-term outcomes.
🔗ntlms.org/BlackMSExperience#BlackMSExperience
ALT Past participant quote that says, "Love that the experience was relatable and felt comfortable. Our resources feel small and this outlet allows for us to feel included in the conversation and hopeful."
Today is #WorldM0Day - May 30, 2022 🧡
Today we celebrate our mothers, an aunt, a cousin, an old friend, those we have lost, those living with #MS, and everyone affected by MS‼️ Get Involved. Take Action. Donate.
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#USvsMS#May30#WorldMSDay2022#MultipleSclerosis
The Black MS Experience Summit is focused on Empowerment in Healthcare, featuring dynamic stories and speakers who will address navigating and overcoming challenges in the healthcare system. Join us June 15-16: ntlms.org/BlackMSExperience. #BlackMSExperience
Sleep is a cherished commodity in most households, but those with MS especially understand its benefits when battling MS fatigue, stress, or pain.
Read this week's article to glimpse Digmann's perspective on his relationship with rest: msfocus.us/sleep.