Ongoing struggles recovering from my second stem cell transplant in six months make it easy to write compelling posts. But enough already! I was admitted to our local Baptist hospital last night after an emergency room visit that revealed I had pneumonia that was getting worse by the hour.
One of my pet peeves: when celebrities don’t disclose the type of cancer that they’re battling. They could at least devulge it in their obituary. Most of the rest of us disclose it. Obviously I’ve done so much more. I’m not implying everyone needs to be as open as I am. But come on: inquiring […]
Rough weekend. As I explained in a post last week, I’m not used to backsliding–post transplant–once I start improving.
A lot has happened since I ran two of the final installments about the importance of controlling blood glucose by Danny Parker:
Blood Glucose, MGUS, Myeloma & Metformin (Part Seven and Eight)
It’s official. We didn’t win the Powerball jackpot. One of our tickets did match three numbers, so I should get most of my $20 back. Turns out there were three winners, so there “only” would have been 300 million available to donate for myeloma research. It would have been fun to see what kind of […]
These are the posts I dread writing. One of my closest myeloma friends, Sara Lathan, from Charlotte, North Carolina, lost her extended fight with multiple myeloma earlier this week.
Monday morning my email inbox lit up. A Wall Street Journal article–both online and in the hard copy edition–about the FDA’s unprecedented approval of three anti-myeloma drugs in less than a month was featured front and center.
I understand that all of my reader’s don’t celebrate Christmas. After all, myeloma doesn’t respect religious or political boundries; it’s an equal opportunity dose of misery. Even so, I thought that Christmas Eve might be the perfect time to catch up on how some of our friends we’ve been following this past year are doing.
I experience countless emotional moments as I hear from myeloma patients and caregivers from around the country and sometimes, around the world. I wanted to share an exceptionally personal one with you here today.
I’m feeling a much better today. I was in such a dark place. Feverish and saddled with abdominal pain and now nine days of diarrhea, To be wheeled from ICU up to the BMT unit was discouraging beyond words. But as so many of reminded me with love and certainty, “It will get better!”
Thanksgiving is all about family and friendships. I have made some amazing friends during my myeloma journey. Some I’ve never met. We’ve simply emailed regularly for years.
Having undergone yet another stem cell transplant, I’ve learned one thing you can count on: expect complications.
This is Michele. I had met several of you at last year’s Pat’s Myeloma Beach Party. Pat is still pretty weak. He is definitely looking forward to feeling like himself again.
A number of you have already contributed to help CrowdCare Foundation fund a pair of cutting edge T cell trials in Germany and John Hopkins in Baltimore. THANK YOU! For those of you on-the-fence, I wanted to share some good news.
More pictures from last weekend? Why not? Tomorrow is another college football Saturday. I’ll share more then. But first I wanted to follow up on a very serious subject: reader responses to Tuesday’s post, pleading for emotional help and support for me and my fellow myeloma patients and caregivers:
Myeloma patients need emotional support
I’m so proud of myself! I finally figured out how to download pictures from my Android smart phone to my laptop. It’s no secret that I’m tech challenged. And it isn’t about age: old timer, good friend and fellow myeloma survivor, Gary Petersen, gave me a tutorial at a patient dinner meeting on Tuesday.
I’ve had to make some pretty tough therapy decisions lately. It got me thinking. Where do patients like us go for emotional support?
I’m sorry that I haven’t been more responsive to reader’s comments on the blog, Facebook and Email. Pattie and I just completed another “never a dull moment” series of flight delays on our way to Madison, Wisconsin to see the University of Wisconsin play the Iowa Hawkeyes Saturday.
I’m a fighter–and I’m stubborn. I’m focused and willing to do just about anything to help extend my life.
Last week we caught up with allogeneic stem cell transplant recipient, David from Tampa. He’s doing well, but the allo did not wipe out his myeloma–and his new immune system still may not recognize it as an invader. Today let’s hear from Tom. Like David, Tom’s doctors tried an allo as a way to hit […]