by Meg | Mar 18, 2019 | living with a disease, living with MS, MS, Multiple Sclerosis, Multiple Sclerosis & Cannabis, Uncategorized
(photo: circa 2009 – location: some campground in the PNW – photographer: Piper S. age 9) The truth is that this is a 10-year-old photo of me…in a bikini, on my Segway… The shameful truth is that I am using it to try and grab your...
by Meg | Nov 19, 2018 | Book, Books about MS, Cannabis Resources, CBD, CBD & Chronic Illness, CBD & MS, CBD & Multiple Sclerosis, Chronic Illness & Cannabis, Chronic pain, Chronic Pain & Cannabis, dealing with disease, living with a disease, living with MS, Medical Marijuana & Pain, MMJ & Multiple Sclerosis, MS, Multiple Sclerosis, Multiple Sclerosis & Cannabis
Really, it should not come as a shock to anyone that lives with MS to hear that the week my book, Segway Into My New Life: A Story of Diagnosis, finally came out on Amazon – my MS decided to throw a temper tantrum and go into a flare. BUT – thanks to my...
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 | 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 | Jul 10, 2017 | Blogger friends, Living with Chronic Illness, living with MS, MS, MS Awareness, MS Blogs, MS Charities, MS Research, MS Resources, MS Support Groups, Multiple Sclerosis, Time management, Uncategorized
I have a confession to make to any and all other people that are living with Multiple Sclerosis (and other chronic illnesses) that I have connected with; either here on my blog, via various different social media platforms or through the many websites that gather...
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...
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