Good morning, @ntsimpson. That’s incredible news about the funding and waving protocol for your husband to be able to proceed with CAR-T Stem cell therapy for his CLL. There are new breakthroughs with CAR-T all the time as this field continues to be applied to more forms of cancer through constant research and development.
I agree with you that the word ‘caregiver’ doesn’t reflect the enormity of the challenges faced, sometimes equal or greater than that of the patient, sans the direct medical aspect. My husband and I went through similar with my AML/Bone marrow transplant odyssey! Nothing in our married life of 45 years at that time could have prepared us for the adventure that lay ahead! It’s a challenging roll, to be sure. If you find better term for Labor of love servitude I’d love to hear it! LOL. My husband was rock solid through that really rough year and I watched him age, even though he says ‘he was just fine’.
You and your husband have an equally challenging adventure ahead. He’s on the cutting edge of science with the application of CAR-T for his CLL. It sounds as though you both have a wonderfully positive attitude and know how to find balance in your life. Going through this it’s key to keep that positivity, have a sense of humor and sense of adventure and also being adaptive. We found those 4 traits to be the most beneficial to get us through the worst of times. It all paid off with 5 years being cancer free and feeling as though nothing ever happened.
I know your husband isn’t having his procedure at Mayo, but I do have a helpful guide I received with my bone marrow transplant that might be helpful for both of you. You’ll notice on the first page is a menu. Scroll down to the 3rd section on CAR-T for information about your husband’s upcoming procedure. There are also great tips on caregiving, post transplant care, etc.. https://connect.mayoclinic.org/blog/caregivers-for-bmt-car-t-and-hematology/tab/transplant-journey/#CAR-T
Will you have to relocat temporarily while your husband undergoes his treatment or are you near the clinic where this will be taking place?
No, we are lucky and do not have to relocate. While we have a CLL dr at the Mayo, this was always a second opinion. My husband is a resident of Canada. Thankful that his Mayo dr told us to get on a plane fast in March and go back to Canada. He knew if we stayed in the US we’d go bankrupt, as we pay the Mayo out of pocket. In the US if you have no insurance with any of these severe illnesses you are out of luck, and even with insurance, these companies are often unwilling to fund state-of-the-art treatment. Long live the Canadian healthcare system.