by Meg | Nov 21, 2016 | CAM, Finding a doctor, MS, MS doctor, Multiple Sclerosis, Neurologist, Uncategorized
Finding a doctor that you trust, someone that instills a sense of support and validation while imparting knowledge in a way you can understand can be difficult in the best of times. But finding that special someone while feeling like shit and scared as hell can be...
by Meg | Nov 3, 2016 | B12, dealing with disease, MS, MS and Vitamins, MS doctor, MS Support Groups, Multiple Sclerosis, Multiple Sclerosis & B12, Multiple Sclerosis & Vitamins and Supplements, Uncategorized
Yesterday, on my way in to see my doctor I shared this pic on social media along with the caption “Heading in to dr appointment to have B-12 levels checked again. Was super low at last appointment and dr wanted me to come in weekly for shot BUT I...
by Meg | Jun 11, 2013 | Biogen, dealing with disease, disease modidying drug, DMD, living with a disease, living with MS, means of mobility, MS, MS doctor, MS drugs, Multiple Sclerosis, Neurologist, positive attitude, segway, Tecfidera, using a cane
I have said that I will keep you updated on what is happening with my latest and greatest med – Biogen’s Tecfidera, and I will, but first wanted to share my story about “OH FUCK.” I was diagnosed with MS in December of 2007, Merry Christmas to...
