I began this blog as a way to release the fear that seemed to seep from every part of my body after I learned that my honey had Multiple Myeloma. It has often become my way to lighten the read, and the journey, by retelling the sometimes humorous antics that can occur with us. I often add medical data, notes and photos, as they've applied to my honey, whenever I feel that other MM patients, or their caregivers, may benefit from the information. Very seldom, if ever, do I delve deep into the medical field. I leave that to those who have been around this cancer longer than I, and are more knowledgeable bloggers like Margaret's Corner or Pat Killingsworth, or the MM Specialist like Dr. James Berenson, and so many others.
Often, when things aren't going well, when the pain feels as if it's ripping at my heart and tearing at my soul, I allow my feelings to pour onto the paper like water poured from a pitcher. As I wrote, in one of my first posts, it's okay to cry ......and it's okay for others to know that you cry. I have laid open my heart, and my soul, for all to read and understand how this terrible disease has affected me, and our family.
We who live with Multiple Myeloma live for each day and for a cure, but we also exist in reality. We know that life can change in a second. We are excited and can experience joy in the smallest of things - like an M-Spike (monoclonal protein) that has dropped even a tenth of a degree (it should be zero). On days when our loved one awakens, with a smile, and says "I feel good", it's as if a blessing has been bestowed on us. We love those days when things go so well that we can "almost" forget they have cancer. Those are the days when we turn our eyes heavenward and say "Thank you, Lord".
There are also those days when their pain is so unbearable that each step takes their breath away. Those days when we want to question and say "Why him, Lord?" Those days when the pain doesn't allow them to move, once they are settled and comfortable. Those days when you hear them whisper, "I don't think I can take this anymore." Those are the days that bring tears to your eyes, and a lump to your throat, and the days when I beg "Lord, please let me have him for just one more day."
Even though our numbers are spread across this United States and many countries of this world, we don't fight our battles alone. We have forged friendships through the many avenues made available to us on The Myeloma Beacon , and the Multiple Myeloma Support List at Acor, the responses in the forums on these websites are remarkable. The Multiple Myeloma Research Foundation , founded by Kathy Giusti, herself a victim of Multiple Myeloma, is a non-profit organization which is not only leading the race in donations to find a cure for MM, but is educating the public about this terrible, incurable disease. And, of course, Facebook has forged friendships worldwide........strangers who have become friends, because of MM.
Two years ago, I knew nothing about Multiple Myeloma and the devastation and heartbreak it brings to families. I had no knowledge of Velcade or Revlimid or Dexamethasone. What were bone lesions? And, how painful could a compression fracture be? I didn't realize that pneumonia, or kidney failure; or something simple, like a sinus infection, could bring almost instant death.
This holiday season seemed to be hard on those with Myeloma, and for that reason I chose to write this blog. We become friends and soulmates because of the lot we've been given, and four of those friends did not make it through this holiday. There are those, with MM, that have lived for years.....and then, there are those, that God chose sooner. Each patient, each treatment is different. Why one lives longer than another, is yet unknown. We are only happy for the days we've been given, but we constantly pray for many more.
Gene Autry wrote the first version of this old western song, and over the years even though the lyrics have been changed by other vocalists, the meaning remains the same.
Have I told you lately that I love you?
Have I told you lately that I care?
Have I told you lately that I need you?
Well, darling I'm telling you now.
It doesn't matter if you have Myeloma, or if you're fit as a fiddle.....it just never hurts to say........"Have I told you lately that I love you?"
And, most important, "Thank you, Lord, for another day."
Oh my, you've said, so eloquently, everyithing I feel on a daily basis. Thank you...
ReplyDeleteAngie: When you write.....I know exactly how you feel. Remember, we are in each other's heart!!
ReplyDeleteHugs.....
Thank you Sarah! Jeff and I had one of those evenings tonight when we almost forgot he was sick. We enjoyed dinner and Christmas shopping :) You're absolutely right, every day is a precious gift.
ReplyDeleteRene: Those are the days that I absolutely love....when I can push MM to the back of my mind.
ReplyDeleteSo happy you were able to enjoy this day....and others!!
Hugs
A wonderful post, Sarah. And such an important message ... treasure the gift of another day ... each one is so very, very precious.
ReplyDeleteDianne: Thanks.....it really is important, and MM made me understand that I should take nothing for granted!
ReplyDeleteHugs.....
That's a lovely post.
ReplyDeleteNow I am singing along!
Roo: Thank you....have a great holiday with all your creative talents!!
ReplyDelete