Working at the Multiple Sclerosis Association of America (MSAA), I am often asked if I have a diagnosis of multiple sclerosis (MS). While MS is not part of my personal journey, speaking with people living with MS has given me a unique perspective on the importance of listening deeply, respecting each person’s experiences, and recognizing the power of self-advocacy. Their courage in navigating uncertainty and speaking up for their needs has helped me see how vital advocacy is in every health journey. Every conversation reminds me that every voice matters and that advocacy, whether for oneself or on behalf of others, plays a powerful role in navigating life’s challenges.
Continue readingTag Archives: MS Awareness Month 2026
Autoabogacía en acción: Aprendiendo de quienes viven con EM
Al trabajar en la Asociación de Esclerosis Múltiple de América (MSAA, por sus siglas en inglés), a menudo me preguntan si tengo un diagnóstico de esclerosis múltiple (EM). Aun cuando la EM no forma parte de mi historia personal, convivir con personas que viven con EM me ha dado una perspectiva única sobre la importancia de escuchar atentamente, respetar las experiencias de cada persona y reconocer el poder de la autoabogacía. Su valentía para afrontar la incertidumbre y expresar sus necesidades me ha ayudado a comprender lo importante que es la abogacía en cualquier proceso relacionado con la salud. Cada conversación me recuerda que todas las voces importan y que la abogacía, ya sea por uno mismo o en nombre de otros, desempeña un papel fundamental a la hora de afrontar los retos de la vida.
He escuchado historias de personas que abogan por sí mismas en citas médicas, en el trabajo y ante sus familias. Algunas personas descubrieron que hacer las preguntas adecuadas durante las consultas médicas facilitó hacer ajustes en el tratamiento y mejoraron su calidad de vida. Otros describieron el valor que requirió hablar abiertamente sobre sus limitaciones o necesidades, a pesar de sentir miedo o vergüenza, asegurándose de recibir el apoyo que merecían. Estas historias demuestran que la autoabogacía no se trata solo de expresarse; se trata de tomar el control de su vida y de sus decisiones.
La autoabogacía puede darse de muchas maneras y no siempre implica algo drástico. Algunas personas han negociado adaptaciones en su trabajo, como horarios flexibles o equipo ergonómico. Otras personas se han unido a grupos de apoyo o comunidades en línea para compartir experiencias y obtener consejos prácticos. Incluso acciones pequeñas, como preparar preguntas antes de una cita médica o llamar con anticipación para verificar la accesibilidad y el cumplimiento con la Ley para Estadounidenses con Discapacidades (ADA, por sus siglas en inglés), pueden ayudarle a tomar el control de su salud. Abogar por uno mismo es una práctica continua que consiste en valorar sus necesidades y expresarlas de manera constante.
Convivir con personas con esclerosis múltiple me ha demostrado que la autoabogacía es valiosa y profundamente personal. Expresarse, hacer preguntas y confiar en sus instintos no es solo manejar un diagnóstico; es tomar el control de su vida y sus decisiones. He visto el gran valor que se necesita para pedir ayuda, establecer límites y expresar las propias necesidades. Lo más importante es que he aprendido que todas las voces son valiosas. Cada historia y cada ejemplo de abogacía me recuerdan que todos tenemos la capacidad de moldear nuestro camino, y que escucharnos y aprender unos de otros fortalece ese recorrido.
Using Your Voice
By Angel Blair
It can be a truly powerful thing. Yes, sometimes it’s not easy. It can make you feel uncomfortable, unsure, and anxious. But eventually you find that it is absolutely necessary in order to take care of yourself and to put your needs first. It’s finding your voice and using it when situations call for it. It’s self-advocacy, and it is a crucial part of life. Advocating for yourself is a monumental task and one that elicits various outcomes and feelings. An admirable trait that when executed effectively, can evoke feelings of pride and content.
For individuals living with MS or another chronic illness, self-advocacy becomes a vital part of the disease journey. From diagnosis to treatment and care, speaking up for your needs, expressing concerns, and asking questions are necessary components to ensure quality care. There may come a time where you have to question a provider, seek another opinion, or say no in response to something regarding your health. These aren’t always easy to accomplish. But you’ll find that because you know yourself and your body best, it’s essential to make others understand what your needs are.
To do this you have to use your voice, even when others try to shut you down. Sometimes this can feel like a fight, and saying speak up is easier said than done. But if you don’t, you may end up questioning more things than you’d like and wondering how things could have looked differently. The MS disease course can be so unique to those affected that it requires individual accounts, personal perspective, and self-assertion when needed.
It’s hard not to question or doubt yourself if others protest or show doubt in you. It takes belief and faith and proves to be a job in itself. Having trust in the self-advocacy process is difficult. And though it proves to be a struggle sometimes, it’s worth the fight if it leads to what’s best for you and your care. Ensuring you’re being cared for in the best way possible is the ultimate goal and what you rightfully deserve.
It’s National MS Awareness Month!
By Samuel Fitch
The idea of self-advocacy is something that becomes incredibly important when you live with multiple sclerosis or care for someone who does. There are many ways to advocate for yourself, in medical decisions, in treatment conversations, and in daily life. One area that often gets overlooked, however, is how we advocate for our time.
Continue readingThe Power of Self-Advocacy: Finding Your Voice and Owning Your MS Journey
Self-advocacy is more than just a buzzword; it is the act of speaking up for yourself, clearly communicating your needs, and taking action to get what you want in life. At its core, it is about recognizing your own worth and ensuring your perspective is heard and respected.
When you learn to advocate for yourself, you transition from being a passive observer to an active participant in your own MS journey.
Here are a few tips to start being your own best advocate:
Continue readingThe Ongoing Practice of Self-Advocacy
“Self-advocacy” sounds so empowering and clean when you say it out loud. A neat, controlled, confident phrase. It makes you feel like the kind of person who knows exactly what they need and is not afraid to ask for it.
Living with MS and working in the MS space has taught me it is rarely that simple.
Continue readingUnderstanding the “Invisible” Side of MS: When Looking Good Doesn’t Mean Feeling Good
If you are living with MS, you have likely heard those five dreaded words: “But you look so good!” While usually meant as a compliment, for many in the MS community, those words can feel like a slap in the face.
Multiple sclerosis is often called an “invisible illness.” Because many of the most difficult symptoms happen deep inside the body or brain, friends, family, and even doctors might not see the battle you are fighting. This can make describing those invisible symptoms quite challenging.
Continue readingLargest Art Showcase Ever Debuts, plus MSAA’s March 2026 Artist of the Month

For more than 15 years, MSAA has celebrated the artistic talents of the MS community in our digital Art Showcase. This year – for the second year in a row – we are excited to launch MSAA’s largest Showcase to date!
Featuring 94 artists and more than 250 wonderful pieces of artwork, MSAA’s 2026-2027 Art Showcase highlights the inspiring stories of individuals with multiple sclerosis from across the country. We highly encourage you to view this one-of-a-kind Showcase by visiting MSAA’s 2026-2027 Art Showcase webpage.
March 2026 MS Artist of the Month
MSAA features the work of many talented artists affected by multiple sclerosis as part of our annual MSAA Art Showcase. Each month we share these artists’ inspiring stories and beautiful artwork with you as our Artist of the Month. This month, we celebrate Leidy Burgos of Philadelphia, PA as March’s Artist of the Month.
Continue readingYour MS, Your Voice: The Power of Self-Advocacy — MS Awareness Month Highlights & Resources
MSAA proudly recognizes March as Multiple Sclerosis Awareness Month and is pleased to present the MS community with helpful and encouraging resources and programs throughout the month.
Our MS Awareness Month theme in 2026 – Your MS, Your Voice: The Power of Self-Advocacy – focuses on what advocating for oneself really looks like in everyday life. Throughout March, explore self-advocacy from both the clinician and lived-experience perspective as we share practical tools to help the MS community. Please join us for the following free MS Awareness Month activities:
Continue readingAsk the Expert: Visual Disorders
Featuring Barry A. Hendin, MD
MSAA’s Chief Medical Officer
Question: What types of visual disorders may be caused by MS, and are any types of visual issues not typically associated with MS?
Answer: Visual signs and symptoms are common in multiple sclerosis and ultimately affect the majority of people with MS at some time in their lives. Problems occur when there is demyelination of the optic nerve or the brain stem centers that control eye movements.
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