Last month, we asked you to reach out to your U.S. House of Representatives to support "Dear Colleague" letters to support #MSresearch funding – now it’s the U.S. Senate’s turn! Urge your U.S. Senators to support MS research priorities: https://t.co/On7uJA6gJJ. #MSactivist
The connection between #chronicillness and well-being is not just medical. @ims_foundation uses #technology 2 improve quality of life 4 those that are immobile or isolated due to the symptoms of #MultipleSclerosis. Connect to the outside world. Apply now: https://t.co/T2iQaZjT1D
Multiple sclerosis is a chronic disease of the brain and spinal cord, also referred to as the central nervous system. It can be treated, but there is no cure. Symptoms vary , but motor and cognitive problems are the most common.
Read more: https://t.co/kFkAfWL2o5
The moment we will all be talking about tomorrow is the courageous #SelmaBlair, making her first appearance since announcing her MS diagnosis, at the VF Oscar party. She needs a cane to help walk, but she came to prove that no matter how tough this disease, she is a fighter. 🙌
BREAKING NEWS: New National MS Society-led study says nearly 1 million people are living with MS in the United States. That’s more than twice the previously reported number. Learn more: https://t.co/FfJisREpnN #TwiceAsMany#ThisisMS
For many of us, the mental and emotional elements of MS don't get discussed as much as they should, but with 50% of MSers experiencing symptoms of depression, it's #TimeToTalk
With thousands of active MSers online, start a meaningful conversation today on https://t.co/I5FkPY1C7Y
So amazing to see the uplifting stories today as we all #ReclaimSocial - we thought we would share Bonnie's story, whose quality of life improved drastically after receiving an ipad thanks to #iMSConnect https://t.co/4Y5LHQVTPw #MultipleSclerosis#Tech4Good