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 | Mar 16, 2016 | Being Strong with a disease, confidence, disabled, Exercise and MS, Falling down with MS, I have fallen and can't get up, living with a disease, living with MS, means of mobility, MS, Multiple Sclerosis, Pain, positive attitude
Hey all…back from my “winter break with the kids/parents visiting from out of town visit” hiatus. I have good news and bad news. The BAD NEWS is that I had a pretty bad fall. Knees and palms were pretty shredded up, I may have a fucked up wrist...
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 | Jun 28, 2013 | Biogen, dealing with disease, disease modidying drug, disease modifying drug, DMD, living with a disease, living with MS, MS drugs, reasons to laugh and smile, Tysabri, using a cane
This story is from quite a few years ago, shortly after I was diagnosed. We had spent our month back East with my family and begrudgingly had returned to the life and chaos that hits every September, with the kids going back to school. It was about 7:30 in the...
