“I was thrilled to have found this podcast created by two women I love and admire as actresses now sharing their experiences with MS. I was diagnosed with RRMS 27 years ago and was fortunate my first neurologist (UCLA) encouraged me to begin a disease modifying medication (prior to FDA approval). The stars were aligned as the disease progression was nearly halted because of the disease modifying medication. Other than lasting effects of optic neuritis, I have continued with exercise (running, hiking, and more), working, and raising two sons who have brought joy even with challenges from MS (and challenges from parents dying, marriages ending, etc.!). Finally, volunteering for National MS Society (SF) has brought hope that an MS cure will be found while fighting for access to medications in the interim so critical to MS patients. Brava for hosting this wonderful new podcast so desperately needed! Christina”
Marin Open Ears via Apple Podcasts ·
United States of America ·
03/15/24