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Showing posts from 2020

Better Luck...

  2020 has been such an eye-opener in so many ways. The idea that life can be snatched right from under us has and is a reality that many try to avoid. COVID-19 showed us who was boss along with so many lessons. First Looks Can Be Deceiving- I think some in the myeloma community can agree that this virus has allowed many people to truly understand the importance and what happens when our immune system is compromised. The look of healthy, fit, never sick was not the case for many this year. I know for the many years living with multiple myeloma, many people didn't get it. Many didn't understand what a compromised immune system means, and how dire an infection could turn our situation from bad to turmoil in a quickness. The face of "got it together" has opened up the dialogue that the look of being ill has different faces, situations, and timelines. Second Family and Grounded If you've been the jet setter, or spend days seeing your family at night while being away a

New Way of Movement

It’s been a while to post but this hasn’t slowed me down to handling the things I have on my plate. When COVID 19 hit like so many there was a huge concern, and still is in regard to what this virus means. It was also a concern in what It means for people with underlying issues such as myself. When we hit into the second month of quarantine did I move my concern to action by reaching out to my team to get my blood work tested. My greatest fear was would my present remission state change due to this virus? As I’m sure there are many people worried about similar thoughts. We were at a point where for many we could not reach our doctors for a one to one appointment, and that is scary and frustrating for anyone with cancer. What do you do when you’re totally alone in this or feel like you’re in it alone? Questions I’ve been active on the circuit talking with other cancer survivors during this time, and I tell you it’s been quite scary listening to others express their fee

Multiple Myeloma Podcast

Hi There, I'll be teaming up with my buddy Kenny Capps for a cool podcast on everything thing myeloma. We hope to give a different outlook on topics and what is on the mind of many young adults affected by the disease multiple myeloma. More details to follow soon. Email me for more information- madaboutmyeloma9@gmail.com