Multiple Sclerosis Information Center
Living with Multiple Sclerosis can feel overwhelming, especially when we are looking for clear answers and real support. That is why I created this Multiple Sclerosis Information Center, a space where I gather the resources that have helped me understand my diagnosis, my symptoms, and the advances that have transformed the way we live with MS.
Here you will find reliable, up-to-date information explained from a human perspective: what you need to know. Remember that you are not alone; this is a place to learn, explore, and feel supported.
Below you will find all the resources organized so that you can quickly and easily access everything you need today. You can also read my blog.
I share everyday reflections, emotions, practical tips, and educational content about multiple sclerosis. A supportive community where you can feel accompanied and understood.
Here you will find a selection of specialists, research centers, and official websites that have accompanied me on this journey. These resources have been validated, updated, and created by experts in multiple sclerosis information, so that you never feel alone and always have reliable, clear, evidence-based guidance at your fingertips. You will find valuable information and peace of mind on this journey.
Dr. Aaron Boster, specialists on MS. His clear explanations and human approach have accompanied me for years. His medical center offers information on MS based on evidence and a comprehensive approach to patient care.
One of the world’s most comprehensive sources for understanding the global impact of multiple sclerosis. Here you will find up-to-date statistics, international studies, and data that help to gauge how this condition affects millions of people.
One of the most important organizations supporting patients and families. It offers practical guides, emotional resources, self-care tools, medical updates, and support programs for different stages of life with MS.
The leading organization in Europe dedicated to research and education on multiple sclerosis. ECTRIMS shares recent studies, conferences, advances in treatments, and essential scientific insights to help you stay up to date.
The North American counterpart that promotes research, publications, and specialized events. If you are looking for information on sclerosis based on the latest scientific findings, this resource will help you understand where treatment and research are headed.
My space for in-depth conversations with specialists: neurologists, physiatrists, psychologists, therapists, and healthcare professionals who have been key figures in my journey. Clear, humane interviews full of answers that I needed at the beginning. Subscribe to our channel! And follow the conversations with Victoria too!
When I was diagnosed, finding answers was difficult. There wasn’t much information available about multiple sclerosis, and I didn’t know where to start. It took me years to discover reliable resources, recognized experts, and communities that truly understood me. Today, I want to make it easier for you.
Here is everything that has helped me the most, gathered in one place.
I want this space to be a hand on your shoulder when you feel lost, a map when you have doubts, and a friendly voice when you need to understand what is happening with your body or your emotions.
I am not a Healthcare Professional, I do not have a Medical Training.
In my project, Living with Multiple Sclerosis, I share my personal experience and the tools or habits that have been useful to me. Nothing published here should be considered medical advice or a medical diagnosis. You should always consult with your healthcare professional before making any decisions about your treatment.
Join us in this project, comment, and
if you have any topics of interest you would like us to cover, write to us. Share our project with everyone you think might find this information useful.
You can write to me at this email address:
victoria@viviendoconesclerosismultiple.com
Hugs!
Victoria