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You are invited to Letters to the MonSter

https://www.youtube.com/watch?v=serV18MirGg

Well, the sun is shining at last and it appears that spring is sincerely here and hinting at summer weather.    That means I need a summer project; hopefully one that I can complete. With two young adult books   in various levels of completion, you will surely tells me how ridiculous I am to start yet another writing project. but, inspiration has no rules, right?
           The entire month of March MS Awareness Month led to so many
awesomeavenues of expressions, fueling my need to share and learn with 
fellow MS Warriors. So, let's hare. Let's learn. In Letters to the MonSter, 
my goal is to allow fellow Warriors to vent, scream, rant, and exorcise the  MonSter out of our lives. Let's unite in this project to erase multiple sclerosis from our lives. As Leslie Hillburn stated in the preface to my last tome to this disease, "...the ONLY place you will get any support and understanding in dealing with me (MS) is with Other People wi…

Dental care and MS

Having an autoimmune disease makes every aspect of living a healthy life magnified in comparison to that of a healthy individual. Multiple sclerosis magnifies the effects of every little nuance life tosses our way. The common cold is n longer a little sniffle fest. Stress headaches evolve quickly into migraines. Solving the soduko in the morning newspaper turns into a major college exam.

In my case, I have experienced ridiculous dental issues. At the age of thirty-two I elected to pursue the dream of having perfect teeth. Getting braces sounded a bit odd to my friends, but I could now afford the financial burden and I believed I was mature enough to truly be responsible for the process. 

Call me weird; but I totally enjoyed the process (I don't care). My students even got a kick out of it, especially when they taught me how to "fling" my rubber bands with my tongue. (Such a cool weapon.)

Upon braces removal day, I swore to be religious about wearing the retainers. And I did…

A Sea of Orange Hope

With a forecast for rain and cool temperatures, many felt the 2018 Walk for MS might be a sloppy mess; but when I arrives in Morgantown, West Virginia, I found an optimistic, celebratory atmosphere that no storm could dampen. Clouds dispersed and skies cleared, knowing that the heavens  could not compete with the storm happening on the ground at the  Waterfront.







The true champions had arrived and their name was Warrior.



Tents were erected, tables arranged, team shirt distributed, books stacked, (I got to share I Have MS. What's Your super Power? !!!!)






acknowledgements made, participants in place, and the walk began,






















with Team Tiffany in the lead. My new MS friend, Tiffany Albright, is an inspiration. she single-handedly recruited an amazing team of walkers that outnumbered any other congregation in attendance. Her numbers were amazing in monetary contributions and the enthusiasm of her teammates was more than inspiring. 

Event though I did not personally join the walkers, my day was fu…