The MS Mobility Foundation is a non-profit organization that is dedicated to making people disabled by MS mobile outside their home.  There is currently very little to no funding for this.  There is a desperate need for this kind of help.  The Foundation is new, and we are in the process of submitting grants to be able to start making people mobile!  But we need YOUR help!  Visit this website, and visit it often.  Sign up for our monthly newsletter, and most importantly share this cause with your friends.  The ONLY way the Foundation can get funds is by letting donors know that there is a need.  Even if you are mobile, there are so, so many who are not, and they need your help.  Please do what you can, and be a voice for those who have lost mobility.  For more information please click here.

We are not medical professionals, nor do we intend to provide any medical advice to anyone. Please see your family doctor or neurologist if you have any health care concerns.

Our intention is to provide accurate information from the perspective of informed patients, and caregivers. We have found a need for a community of people battling the infinite hurdles of living with, or loving someone with MS.  It is our hope that you find the resources and support you need to live your life with MS to the fullest.  We have made every effort to provide an honest and accurate setting in which this can be possible.

We are very concerned that what you find here is factually correct to the best of medical science's knowledge. If you find anything here that is factually incorrect, please e-mail us at contact@mssupportnetwork.com. We, of course, cannot answer personal or specific health questions.  These need to be discussed with your GP or neurologist.

It is my belief that knowledge is power and that people with MS, or any other disease for that matter, should have the option to be actively involved in their own healthcare. They should not to be dictated to by an "expert" who may, for a number of reasons, not fully involve the patient in the decision making process.

In order to take part in these decisions, it is vital that we are well-informed. We see things differently to doctors, we actually have the disease and its fickle whims directly affect our lives. We have the right to dictate our own health care choices using medical professionals purely as advisors and effectors.