
Sharing my musings while living with Primary Progressive Multiple Sclerosis (PPMS)! Come on this journey with me…

Covid Came to My Home
Covid came to my home for the first time almost 2.5 years after the start of the pandemic. It was May of 2022. Some might ask how did we go so long without getting Covid? I'd like to say OCD-type precautions from all 3 of us: the hubs, our daughter, and Moi! [And yes,...

PPMS Research
There appears to be a paucity of primary progressive multiple sclerosis PPMS research. So I have decided to compile a list of what I have, so that anyone like me who is interested can hop on board with whichever one fits. So far since my diagnosis, I've been part of...

The Disc Herniation Saga
We need to have a convo about the disc herniation saga that occurred very recently. Grab a drink, will ya? Not that drink! 🤣 [Full disclosure, I wrote this last year and never posted it. Then I actually had another episode this year. As in, the last 2 months. That...

MS Research Opportunity!
The Research How would you like to participate in MS research? Look no further. Here is an important IG live with Dr. Terry Wahls on a remitting relapsing MS research opportunity. And I thought warranted its own blog post. Wouldn't you agree that research is that...

What’s Going On In MS Land? Are You Utilizing Support?
What's Going On in Ms Land with Dad's Visit? What's going on in MS land these days? Well, what had happened was, my father came into town. And for almost 2 weeks, I did not record a single lesson in MS Masteryâ„¢. Welp! Prior to that, I was doing great on knocking out...

Mental Wellness and MS
Let's talk about mental wellness and MS. Now, before we dive into the deets, kudos to this sentiment that we're now pushing, that mental health is simply health. I am completely here for it. I hope you are too! I choose to use the term mental wellness as opposed to...

A Little About Me
I am Dr. Folake Taylor, and I live with Primary Progressive Multiple Sclerosis PPMS. After 15 years in internal medicine primary care, while battling disability/ PPMS for the last 7 of the 15, I found myself diving deeper into holistic health for answers. Now I’m turning my lemons into lemonade. I refuse to allow physical and cognitive disability to stop me, from fulfilling my destiny of using my voice to benefit the world with my knowledge, which I did prior to my illness. Sharing what I have learned and am still learning about the body’s ability to heal itself, which is quite different from what I learned in medical school, is now my mission. I created an online program for MS recovery called MS Mastery™, and I will continue to take you along with me as the daily journey continues.
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DISCLAIMER!!!
Lastly, check with your doctor before implementing anything new. I am NOT your doctor, though I am a doctor.
This is purely educational, not giving you medical advice, and it is certainly not tailored specifically to you because I don’t have enough information on you to do that.