When the Fire Dies

I'm really blessed to still be able to live life to the fullest! My book "Another face of multiple myeloma" is in the works of being promoted, my company Spitfir Productions is nicely being upstarted, Mae's Breath Foundation is making great leigh-way in lung cancer awareness, etc, etc...

I don't know what would happen if my fires goes out; as it's the thread that is truly keeping me alive.
I have a weekly meeting that takes place every Tuesday, and I don't know what it is that gets me so uptight and not nervous but annoyed by presenting at this meeting- but today I wrote the letters-
UCDI- You Can Do It...
to remind me of the light that is in me, and no matter my anticipation weekly tested that I'm doing despite my fears, anxiousness, or what have you.

I may not be perfect with this task, but God only knows and shows me everyday I'm truly a living Spitfire because I'm doing, learning, and achieving in so many other factors of my life.
Who can ask for more....

Screw Myeloma- how dear it tells me how to live!
Cheers to life!

Comments

Plugging Multiple Myeloma

I had a wonderful conversation with a new friend on the trials of myeloma, and it was interesting that we’ve both experienced to some degree the nonchalant reactions when faced with our disease. The saying to walk a mile in one's own moccasins could never be far from the truth, sometimes you get the feeling that no one cares or your cause and or experience is not of interest...., or better yet taken seriously.... I'm reviewing various sources to promote Another Face of Multiple Myeloma , and after extensive research I found there a not many books on patient related experiences, which I find odd, with the exception of popular myeloma blogger Pat Killingsley, I found just two other personal stories from author's penned memoirs on myeloma, and one unfortunately passed away and the other I'm desperately trying to gather contact information. I was in the process of working with a top myeloma foundation to present my book to readers that could possbly relate to my experi

Mud Girl Obstacle 2023

This was my first race that was a thrill to take part in. Multiple Myeloma has been a crutch that I've been able to keep at the back end of my shoulder. It is essential to keep living and doing which I tend to do at the 10th degree. Despite the labels, the Mudrun race was a new thing to do and crush. I live by breaking the rules and breaking those assumptions that life stalls. We do know life is short and I find it my kryptonite to not allow the powers that be which sometimes are out of my control to limit what I want to do; perhaps Im fortunate in being able to do things with some limits of course with a different mindset than most. Crushing this feat of a 3-mile race with 17 obstacles in the mud, and making it through my fear of heights has now allowed me to consider other bucket list possibilities within reason to take a stab at. Cheers to living your best, even when the "You" has been tested at all degrees. Courtesy: Spitfir Production Courtesy: Spitfir Production

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Another Face..... Of Multiple Myeloma

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