It has been a very long time since I last posted, but now is a great time to share some info for those of us on the MM journey and how to protect ourselves and stay up on the COVID-19 threat.
Please follow the link and stay safe out there everyone.
The coronavirus is on the minds of global citizens and all myeloma patients. Dr. Joshua Richter shares an incredible amount of information for myeloma patients to navigate their care in these uncertain times. He shares drugs patients may want to ask their doctors about, considerations for stem cell transplant, the status of some myeloma clinical trials, tradeoffs of using IVIG, and potential therapies being used to treat the coronavirus. This is a must-read show to learn how the coronavirus is affecting myeloma patients and how they can be prepared.
READ IT ALL HERE >>
The search for new drugs that control the continuous relapses of multiple myeloma is still required. Here, we report for the first time the potent antimyeloma activity of amiloride, an old potassium-sparing diuretic approved for the treatment of hypertension and edema due to heart failure.
Read the Full Report
Is Sleep Apnea a way to a cure or treatment for MM?
“Sleep apnea can drive the development of aggressive multiple myeloma in mice resistant to the cancer, a study found, suggesting that the sleep disorder is a modifiable risk factor for this disease.”
Read it all here >
As another year comes and goes, having a diagnosis of Smoldering Multiple Myeloma makes it a bit challenging as you don’t know whether to be happy that you are a year older or that your cancer has not started acting up.
Wow, that is a depressing sentence.
To be true, after almost three years since my doctor told me what was up, I have settled into the routine of “life as normal” since my cancer has remained in the same state… active but not aggressive.
I can say that I don’t think about it day in and day out unless I read something about Myeloma or my three month blood work notice comes up in iCal. I have learned to live with it and am not letting it dominate my thought process.
That’s not to say that sometimes I get hit with a wave of “Oh my God, I have cancer”, cuz I do, but not very often.
At the end of the day, I know what I have so that is power, I have support of doctors and family who are cheering me on every day, and I have done all that I can do to be a healthy person with or without cancer. Really, that is all any of us can do.
So, there it is. Another year living with a cancer diagnosis. Another year of maybe this year, but also another year of live as normal or as normal as can be. That is pretty good and if 59 comes the same way, I will consider that a win and just copy and paste this post then.
Hugs to all,
The expansion part of a Phase 1/2 clinical trial testing tinostamustine in relapsed or refractory blood cancers has begun treating the first patient.
READ THE ARTICLE HERE
Venclexta trial deaths force AbbVie, Roche to stop recruiting myeloma patients
Deaths Halt Drug Trials – READ MORE