by Meg | Apr 9, 2018 | disabled, living with MS, means of mobility, MMJ & Multiple Sclerosis, MS, MS Awareness, Multiple Sclerosis, Multiple Sclerosis & Cannabis, Multiple Sclerosis & Positive Attitude, Multiple Sclerosis & Traveling, positive attitude, Traveling with an Invisible Disease, Traveling with MS, Uncategorized, using a cane
Smiles and laughter are infectious! People are drawn to other people that seem genuinely happy, who seem to be loving life. Because ultimately ALL of us want that, to be happy and to love life. This past week we traveled to Syracuse New York, which REALLY is...
by Meg | Feb 5, 2018 | Chronic Illness & Cannabis, Living with Chronic Illness, Medical Marijuana & MS, MS & Traveling, Multiple Sclerosis & Cannabis, Multiple Sclerosis & Traveling, Multiple Sclerosis & vision problems, Traveling with a chronic illness, Uncategorized, using a cane
“You should come to the Expo in Denver this weekend.” That one simple message I received from an IG user would have a much larger impact on me than he could ever know. What he was proposing was bigger than anything I have done since shooting babies out for my...
by Meg | Jul 17, 2017 | Being Strong with a disease, Chronic pain, Chronic Pain & Cannabis, divorce, Exercise and MS, living with MS, Multiple Sclerosis & Exercise, single parent, using a cane
Exercise and keeping your body moving can help counter the effects of Multiple Sclerosis, increase energy and balance, ease symptoms and even help with cognitive issues. I think we can all agree that this is known and accepted information? No false news in that...
by Meg | Jan 12, 2016 | Avonex, Book, Books about MS, dealing with disease, Falling down with MS, living with a disease, living with MS, Motivational Speaking, MRI, MS and spinal tap, MS doctor, MS Resources, Multiple Sclerosis, Neurologist, Problems with Sex and MS, sex, sex and ms, Uncategorized, using a cane
As you may know, I recently found the time to put together the list of all of the Multiple Sclerosis Resources that I have found over the past few years. One of the sections that I was most excited about putting out there for the world to see and use was the list of...
by Meg | Aug 30, 2013 | dealing with disease, divorce, living with a disease, living with MS, MS, Multiple Sclerosis, Uncategorized, using a cane
When I was given the FINAL diagnosis of having MS and my response was an immediate “oh fuck” my neurologist at the time argued with me that it was an “oh damn” moment, and now, years later, I agree, but at the time, I thought he was a nut job. ...
by Meg | Jul 12, 2013 | disease modidying drug, disease modifying drug, divorce, DMD, living with MS, MS drugs, Multiple Sclerosis, New BETTER, parenting, single parent, Tecfidera, Uncategorized, using a cane
I am going to start off with a quick up-date on the Tecfidera, as I don’t have a whole lot to say. I figure for those that are visiting here because you have googled the drug and found this blog, I don’t want to “force” you to read a whole...