by Meg | Oct 25, 2018 | Books about MS, CBD & Multiple Sclerosis, dealing with disease, living with a disease, Living with Chronic Illness, living with MS, MS, MS Awareness, Multiple Sclerosis, Multiple Sclerosis & the Future, Uncategorized
HOLY SHIT!!! I am a published author – or maybe I have to wait for someone to actually buy a copy to officially call myself a writer?!?!?!? CLICK HERE TO VIEW AND PURCHASE MY BOOK ON AMAZON I am freaking out and feeling proud all at the same time –...
by Meg | Oct 18, 2018 | Chronic Pain & Cannabis, dealing with disease, Disease & Depression, Living with Chronic Illness, MS & Depression, MS & Mental Health, MS Flair, Multiple Sclerosis, Multiple Sclerosis & Cannabis, Multiple Sclerosis & Positive Attitude, Multiple Sclerosis & the Future, Multiple Sclerosis and Smoking, Uncategorized
One year ago today I was at what I would consider to be my rock bottom. I had been off of any and all pharmaceutical drugs and using cannabis and cbd for over a year. I had found a man that loved and cared about me, my kids were happy and healthy and I had even...
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 | Nov 8, 2017 | Chronic Pain & Cannabis, Living with Chronic Illness, Medical Marijuana & MS, MMJ & Multiple Sclerosis, MS & Terpenes, MS Flair, Multiple Sclerosis & Cannabis, Multiple Sclerosis & Terpenes, Multiple Sclerosis exacerbation, Multiple Sclerosis Flair, Uncategorized
Before getting to today’s post about terpenes I wanted to share what I wrote in middle of the night last night. “It is really hard to not feel like a loser when I have to lie down and take a nap after being awake for less than two hours and have only...
by Meg | Oct 31, 2017 | dealing with disease, living with a disease, Living with Chronic Illness, living with MS, MS & Emotions, MS & friends, Multiple Sclerosis, reasons to laugh and smile, Uncategorized
A few weeks ago, BEFORE the flair up, BEFORE the flu, BEFORE the fear and panic set in, I was on the phone with someone. Someone that I know very well and someone that I know has read anything and everything that I have written about living with this disease. When I...
by Meg | Jun 26, 2017 | Being Strong with a disease, Chronic Illness, dealing with disease, living with a disease, Living with Chronic Illness, living with MS, MS, Multiple Sclerosis, Uncategorized
From day one of my diagnosis, I have heard and repeated the mantra “I may have MS, but MS doesn’t have me!” But, I think I need to amend this a bit… because I am pretty sure that bitch owns me! And I am pretty certain divorce is not an option. We are married for...
