Your Questions Answered – Hear Directly From Dr. Cramer on What This Change Means for You
With a deep sense of gratitude for her years of dedicated service to the Multiple Sclerosis community, the MS Alliance of Virginia presents this candid and informative farewell interview with Dr. Jill Cramer. As she embarks on a new chapter, Dr. Cramer graciously shares the personal reasons behind her transition, offers crucial guidance for her patients navigating this change, and reflects on her impactful journey. We extend our sincerest thanks to Dr. Cramer for her unwavering commitment and wish her the very best in all her future endeavors.
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Katie Meyer to Speak to VTCSOM Students.
The Virginia Tech Carilion School of Medicine (VTCSOM) is employing an innovative educational method known as Problem-Based Learning (PBL) to prepare its students for future careers. Through this approach, students interact directly with individuals living with conditions like Multiple Sclerosis (MS), gaining real-world perspectives on the diseases they will one day treat.
MS patient and advocate, Katie Meyer, will soon be sharing her experience with students in the program for the third year in a row. Katie, who was diagnosed with MS in 2013, has been a dedicated volunteer with the MS Alliance of VA (MSAV) since its founding and currently serves as a co-facilitator for our online MS Support Group Meetings. Katie hopes students will understand the individuality of this disease, “MS manifests differently in each person, and symptoms can change rapidly. Despite these challenges, those of us with MS must constantly advocate for ourselves – with insurance and pharmaceutical companies, employers, and sometimes even our own families who may not fully grasp the nature of this invisible illness. If our doctors can understand all of the moving parts that make up the MS patient, they can then give us better care.” Read full story HERE.
Meet Marion Thomas MSN, NP-C
We are thrilled to introduce you to Marion Thomas MSN, NP-C! Marion has worked with our beloved Dr. Carlos Mora since 2023, and she is eager to continue the exceptional care he has provided to our MS community. Marion brings a wealth of experience and a deep passion...
With MS, Always Remember to Leave a ‘GOTWA’ Contingency Plan
A friend of mine went hiking alone during the warmer months of early autumn. Before he left, he contacted several of his friends via a group chat and let us know when and where he intended to start and the location where he planned to camp for the night. He then...
Federal Court Issues Landmark Civil Rights Decision Enabling Thousands of District Residents with Disabilities to Transition Out of Nursing Facilities to the Community
WASHINGTON, D.C. – On December 31, 2024, the U.S. District Court for the District of Columbia issued a resounding judgment in the class action case Brown, et al v. District of Columbia, finding that the District of Columbia has violated the rights of D.C. residents...
Join the MS Alliance of Virginia Team for the 2025 National MS Society Walk in Roanoke
We are excited to announce that the Multiple Sclerosis Alliance of Virginia has formed a team for the National MS Society Walk, taking place on Saturday April 12, 2025 at Rivers Edge in Roanoke. We warmly invite you to join our MSAV team and be part of this meaningful...
Reasons to Date Someone With a Chronic Illness
Dating someone with a chronic illness, like MS, is a scary proposition to most people. Fear of the unknown, concern over declining health, fear over their abilities, etc. The list goes on and on. When it comes to dating, it’s easy to find reasons to give up on...
The Virginia Energy Assistance Program (EAP) assists low-income households in meeting their immediate home energy needs. The EAP consists of four components: Fuel Assistance, Crisis Assistance, Cooling Assistance and Weatherization Assistance. Click on the flyer for more information.
Our Mission Statement
Provide programs, events, activities and services for people living with MS in Southwest Virginia and the surrounding areas, including veterans.
Educate and empower people with MS, their care partners, friends and family. We will guide people to organizations that may be able to assist with their needs.
Contribute to awareness in the community, including educational programs to young people, first responders and community organizations.
Encourage and expand support groups to include assisted-living facilities, homebound people and help others start upbeat groups like ours.