As you know my father was diagnosed with Mantel Cell Lymphoma in late December of 2010. He underwent chemotherapy which put him into remission until December of 2013. It didn't look like the cancer had returned full blown but there were scans taken and it show a small increase in growth of the lymph nodes in the groin area. 15 rounds of radiation therapy were prescribed and undertaken.
And it did in fact shrink the areas that they were concerned about. But the cancer was active and so a new chemo drug was prescribed and my father began to take it. Unfortunately my father's platelet count also did a nose dive so more tests were ordered and a bone marrow test showed that my father was now suffering with a whole new cancer.
It's called MDS or Myeodysplastic Syndrome. It is also a pre-leukemia condition. The question was...is the Mantel Cell mutating or was this a whole new cancer. So my father's oncologist suggested that we go see a specialist in Leukemia at MD Anderson. She paved the way on Monday and they called on Tuesday and we were on the road to Houston on Wednesday with an appointment on Thursday and Friday.
We arrived at our hotel around 6:30 and called my niece to meet us for dinner. We didn't realize that Wednesday night was also the night for an NBA playoff game and all the restaurants would be crowded. But we managed to find a nice seafood place and ate and talked and had a great time.
We got back to the hotel around 10:30 and we all went to sleep...well if you can call it that. I had a very hard time sleeping just because I was so wound up. Thinking of all the what if's etc. And about the time that I think I fell asleep it was time to get up and get going.
We ate breakfast and caught the shuttle that ferries people back and forth to the hospital.
My first glance at MD Anderson was one of awe. It's not just one or two buildings.....it's a small city of high rises and complexes dedicated to this cancer and that. Children, women, you name it and they have a place for it. It is AMAZING.
As I walked through the front doors with the hundreds of other people that morning I said to myself, "Miracles Happen Here Every Day". Not that we were expecting a miracle, but there is hope that there will be a treatment and that we will have bought time and comfort.
We got checked in and filled out lots of forms and answered the same questions over and over again. It's all about being thorough. In due time we were seen by a registered nurse who works directly with our Dr. She asked a lot of the same questions, filled out more forms and looked over my dads records.
From then on we went from one floor to the next, getting a chest X-ray, giving blood and finally having them check out his port so that they could give him platelets and blood if necessary. It was a very long day. Our last appointment of the day was supposed to be at 4:30 and daddy was supposed to get 2 units of blood and 2 units of platelets. We know that 1 unit of blood takes 2 hours to infuse. So that's 4 hours...that would take us to 8:30...if he started on time. But then there was still the platelets. Platelets go faster but that would still be a least an hour so that would be 9:30..if he started on time. Wellll.......we didn't get called until 8:30 p.m....our day started at 7 a.m. and we're still at the hospital at 8:30! Long story short my father didn't get out of the hospital till around 3:30 a.m.
My father ordered us to go get something to eat and to bring him back something later on. So my brother and I left, got some pizza and beer and I stayed at the hotel while my brother went back and stayed with my dad until it was time to leave. My dad was pretty tuckered out...even if he did not have cancer....he's 83 years old and that's a long day.
Our appointment with the Dr. wasn't until 11 a.m. but he had to get his vitals taken before he saw the Dr. and we weren't sure how long that was going to take.
As it turned out it didn't take long and so we ended up sitting in the waiting room for about an hour.
We were finally called back and we got our time with the Dr. He physically examined my dad, listened to his heart and lungs, physically touched him to see if he could feel the swollen lymph glands and then re-read his records.
Here is what the plan is....Daddy will stay the course with the new chemo that he was on before we left for MD Anderson. It takes several months for the results to become apparent and my father has only had 3 treatments so we will stay the course. The Dr. wants to see him back in a couple of weeks but he also wants him to see a Mantel Cell Expert at the same time. We asked lots of questions and they were all answered. We never felt rushed or that any question was stupid or dumb. You could see the relief in my fathers eyes that he had been given a reprieve of sorts. He has time to correct his current situation and he will be able to attend some very important family events that are coming up.
This picture just shows a very small portion of the MD Anderson complex, but you can see from just this small portion just how massive the system is. Every single building in this picture belongs to MD Anderson.
I know that we don't have a miracle but we do have the possibiltiy of hope that things are going to get a bit better and my father is going to feel better in a little while. And that in a way is miracle enough for us.