Getting diagnosed with and living with MS every day can be overwhelming. When I was first diagnosed, I didn’t know where to turn for accurate information.
That’s one of the reasons why I wanted to get involved and raise awareness—so that people would be as informed as possible and have access to useful tools and resources.
That’s also why this section is now updated with tools for healthcare providers (HCPs) as well. The doctor-patient relationship is one of the most important tools a patient
has during this MS journey. This is a true partnership, where everyone in a patient’s life is a part of an amazing team of people,
all playing incredibly important roles. I am so lucky to have a doctor who is a true partner, and that is my wish for every MS patient. I hope that both patients and doctors
will find these new tools and resources helpful—and thank you for being a part of this community.
My story webisodes
This online documentary series highlights Jack’s inspiring journey with relapsing-remitting MS — and how he doesn’t let it control his life!
Jack and others share personal reflections on life with RMS in the You Don’t Know Jack About MS® blog.
The resources on this page can help you prepare for visits with your doctor and better understand multiple sclerosis.