Acute Myelogenous Leukemia (AML) Support Group
Acute myelogenous leukemia (AML), also known as acute myeloid leukemia, is a cancer of the myeloid line of blood cells. Patients with AML usually present with symptoms such as fatigue, bleeding, infection, prompting medical attention. An abnormal blood test reading will then result in further testing in a hospital with a hematologist to determine AML.
I will keep you and Tony in my prayers in the coming weeks and that this can be sorted out without any complications.
A friend of mine had a very poor prognosis before her SCT. After transplant, she had a bone marrow test that showed a mutation, but no leukemia cells otherwise. She took some chemo for the mutation and is now mutation free. She is coming up on 2 years post transplant soon.
There is hope in this. I want this so bad for your family.
Andy
That is the kind of story we all need to hear right now. I do not feel crushed about Tony, because, if I were a betting person, I would bet that the same thing will happen to him. The course of treatment seems to be very appropriate and he will get through it with ease.''
I hope that you continue to feel well. I am very happy for your progress.
Cliff
But, there was a miracle change in there for us and I am expecting a miracle in there for you too.
Your family is in our prayers...constantly.
With love,
John
As you may know, some of us also frequent the LLS boards for AML and SCT. One of the frequent contributors, a man named Kelly, relapsed after four years, an absolutely crushing blow. They gave him Vidaza, I think. It's similar to Dacogen. It prompted a GVL effect which cleared up the residual disease and he has been clean for the last 5 years,
I can tell you're scared and worried, and understandably so. Now is the time to dig deep into your souls for whatever strength you have left, focus on the task at hand and never stop fighting. You have a whole life to live. Never give up. Don't ever, ever give up. Good luck and Godspeed.
Lou
Although this news is not what any of us want to hear, i am so glad you decided to share. This is a support group not a share stories of rainbows and unicorns. AML is one of the worst dx anyone can have for many reasons. The suddenness of onset, the length of treatment, the survival stats (because they are skewed by mean age at dx), just to list a few things. And yet we live, we lift each other up in prayer, we sometimes we thrive.
You know I'm praying, my church is praying and my small group is praying for your family-for Tony and new precious baby P.
You recently asked me how can this be Gods plan. All I know is He has a plan and it is perfect. If we really believe in eternity and heaven then we believe this life is a vapor. PSALM 144:4 & James 44:4. Then this life is a very small piece of our whole. None of us can fathom what this really means but we have faith in something we can not see or feel. This world is full of sorrow and suffering. Our hope is not here. I do not pretend to have the answers but I know who does. I certainly do not know what tomorrow holds but I know who holds tomorrow.
It is easy to be cavalier when I am not in the eye of the storm so please do not take any of this as judgmental. I have no idea of what you are going through. But the truth of the Good News that Jesus brought to all sinners is irrefutable. ALL my faith, trust and hope is in Him. May He give you peace in the storm. Please know you are in my prayers.
Blessings
Julie
I am so sorry to read this. I haven't been on here for months, but recently posted about Julian. I have been praying for Tony daily for a very long time now. I have quite a list of people. I follow a couple of AML boards on Facebook, and there have been many success stories with DLI's and second transplants. God has given you such an amazing blessing with the baby, and I am confident that He has good things in store for Tony too. I will continue to pray for your family.
Jacki
Hugs --- and tears,
Twilight
You've been a huge source of strength for me, Tony's biggest asset right now is you. Please know that if there is anything at all I can do to help that I'm here. I'm praying for your family's strength and the cure for Tony.
Debbie
I too am sorry to read this about Tony, but have faith that the treatments will work.
Congrats on the baby.
Hugs
Katen
They ran a new genome sequencing test (something that just came available to this field last year) and found one additional mutation, a PHF6 point mutation on chromosome X. It's not highly prognostic in AML (actually occurs in T-ALL a lot) so this doesn't really help or harm or current treatment plan. His Dr mentioned another drug to possibly add in called Desatinib (oral pill) which has good results w core binding leukemia like ing 16 or 8/21. She's going to see if we can get it approved.
Mostly we discussed the possibility of a second transplant. That scares us incredibly.
We laid in bed w Izzy last night after reading her books and Tony said that if he goes into a transplant again he would like to start recording videos for Izzy, stuff that he wants to teach her, in her lifetime, in case he's not here for it.
NEVER once during this have I heard him say something like this, like he wasn't going to be here, until last night. It destroyed me!!!
I did not sleep again, and I am not really sure I ever will again.
Right now, I wish we could give each other a huge hug. Our journeys have paralleled for two years and I think of you often.
Let Tony record those stories. I am an archivist and genealogist. These would be treasures regardless. Maybe you can two will listen to them one day in your old age, sitting in a rocking chair while holding hands and babysitting your first grandchild. We all have to dream.
At best, they will bring smiles; at worse, they will be priceless treasures.
You are all in my prayers in a special way. If you happened to be Catholic, pm me. I will tell you about someone I have begun to pray to.
Love
We have labs tomorrow and then a pulmonary function test and Muga scan next week (just in case we move to transplant) His doc doesn't want any hold ups in case we do.
I still lie awake in disbelief that this is our reality, my mind cannot fathom our lives without him! if this doesn't work, what happens when "the cure" for so many is not the cure for him?
Who will give her shoulder rides, and teach her to ride a bike, or help her with math and science?