Sativex Clinical Trial- Medical Marijuana for Multiple Sclerosis Spasticity

These are my own experiences and not medical recommendations, for informational purposes. Please discuss any treatment plans with your medical professional, doctor, neurologist, or MS Specialist. Click any Link in Red Ink to be taken to links, such as the clinical trial. 🙏🏼🧡 I didn’t really understand spasticity when I was diagnosed with MS. I... Continue Reading →

My Birthday; the Invisible Moment between Rare Disease Day and MS Awareness Month

My disease, Multiple Sclerosis , isn’t so rare anymore; with an estimated 1 million in the US, and 2.8 million in the world diagnosed. I was two weeks away from my birthday in the above photo. My boyfriend had just sent me flowers for Valentine’s Day and a strange tingling is spreading on my left... Continue Reading →

Where is the Wheelchair Kamikaze???

There weren’t so many MS blogs 15 years ago, when I was looking for companionship, comrade, anyone else with MS! I was 25, dealing with the disease for five years and I had met like two other people with it. I was a voracious reader, and I was searching for something, someone. I found the... Continue Reading →

Create a website or blog at

Up ↑

%d bloggers like this: