Top Tweets for #MSAA50
“People living with multiple sclerosis (which includes people with the disease as well as the people who have tied their wagons to them) go through a rather stereotyped course of adjusting to life under altered circumstances..." - Dr. Adam Kaplin for #MSAA50 (1/3)
"I am thankful for the hard work & advocacy of everyone at MSAA, raising awareness on behalf of those of us with MS. If not for them, I'd be forced to personally come to your home -- which I will if necessary..." - MS advocate @myoddsock, MS class of 1996, for #MSAA50 (1/2)
“Being diagnosed with multiple sclerosis 30 years I find strength in paying it forward anytime and anywhere. I truly believe that together we are stronger than MS...” - MS advocate, Rosemarie Collopy for #MSAA50 (1/2)
“Knowing what they [people with MS] are going through makes me want to do everything in my power to help. I believe that as independent content creators, we have to be willing to use our voices to help those in need.” - MS fundraising streamer, @bonks_nordic for #MSAA50
![MSassociation's tweet photo. “Knowing what they [people with MS] are going through makes me want to do everything in my power to help. I believe that as independent content creators, we have to be willing to use our voices to help those in need.” - MS fundraising streamer, @bonks_nordic for #MSAA50 https://t.co/UvuDUvF6RP](https://pbs.twimg.com/media/Eng3BX8WMAIlL4S.jpg)
“You must be the change that you wish to see in the world” - Gandhi
“This is why I support MSAA, diagnosed in 2013 I have seen the change that they make in the world of individuals living with MS..." - Art Showcase participant, Jennifer Reida for #MSAA50 (1/2)
“I’ve been living with MS since 2002. My husband has been living with MS since 2009. We both support MSAA because they spread amazing information, community love, and..." - MSAA Art Showcase participant, Leslie Pino Durant for #MSAA50 (1/2)
“People with MS and their caregivers hope to know that it is going to be okay. MSAA provides that hope. It is such a privilege to be a part of this amazing organization that improves lives every day.” - MS advocate, Michael Hoffman for #MSAA50
“My quote is from Confucius... ‘It does not matter how slowly you go, as long as you do not stop.’” - MSAA Art Showcase participant, Kim Standard for #MSAA50. Kim also shared an additional quote, “Never give up, it could be worse.”
“Don’t ever let MS overtake you. It is nothing more than a blip on your life’s radar. The glorious blue sky ahead is meant for you to fly. And fly, you shall.” - Art Showcase participant, Susan Russo for #MSAA50
RT @MSassociation: "Having MS can be an isolating experience in a time when social distancing is the norm! Now is a time when people with MS need support..." – Amanda “Iris” Vercoe RN, MSCN, BSN, CNRN for #MSAA50
"Having MS can be an isolating experience in a time when social distancing is the norm! Now is a time when people with MS need support..." – Amanda “Iris” Vercoe RN, MSCN, BSN, CNRN for #MSAA50
"Soon after my diagnosis, my old clinical instructor inspired me to reach out to others in this amazing community. I remember the exact words that I needed to hear: 'The way that you’ve changed; the way you’ve gotten things under control..." - Dara S. Gill, PT, DPT for #MSAA50
“Working on behalf of MS patients has been my best work experience and certainly the most rewarding one. It is them who teach us to live our Foundation’s motto…. "Embracing Life...” - Executive Director, Lourdes Fernandez of @femabrazando for #MSAA50 (1/2)
"Caring for someone with MS daily is a journey that most won't understand until you've lived it...MSAA created a strong Black community to support Care Partners with resources and a platform to be heard..." - MS advocate and Care Partner, Karen Foster for #MSAA50
"As a person with MS, I find it comforting to meet others who have the same diagnosis as me. When I was first diagnosed, connecting with other people who had MS gave me hope for the future. I've come to terms with the reality of..." - Amanda Bastien, PT, DPT for #MSAA50
“I have battled with MS since 2010. Since then without medication, I've worked harder at keeping my health and nutrition intact to deal with it better. Know this -- You Can Do Anything & Nothing is Impossible." – Musician, Poet, & Dancer, Candace Giles for #MSAA50
“No one should have to navigate such a complicated and unpredictable chronic illness like MS alone. They say knowledge is power and if I have the knowledge, I am more than happy to empower my fellow MS'r because..." - Cathy F. for #MSAA50
“As someone who has been dealing with this for about 15 years now and nine medications, don’t give up and use your voice. Your story is important. As someone who was trained as an MRI physicist, I can talk your ear off about science..." - MS Advocate, Michael Olex for #MSAA50
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