Jacob Hill's Journey: March 2011

Thursday, March 31, 2011

Jacob is getting ready to go into the hospital for a few days for 2nd round of chemo.
Tomorrow is his 3rd birthday. It makes me cry to know how sick he's going to feel on his birthday.
I HATE CANCER !!

Thursday, March 24, 2011

It's official - Jacob is bald! I'll post a picture later - he's still a cutie. The right side of his face is having a reaction to the chemo and is partially paralyzed. Still cute though!!

Tuesday, March 22, 2011

We got the treatment plan from New York today. Next chemo will be in Dallas then off to NYC on April 20th for stem cell harvest and surgery. He's bounced back from round 1. Playing like normal. He's walking around with my old stethoscope around his neck. He told me he was a doctor. Go Jacob!! His hair is really shedding today. I'm looking for cute caps!!!

Monday, March 21, 2011

Jacob got out of the hospital today. He's only lost a little hair so far. Yea! For a little longer at least. :( He seems to be feeling pretty good which makes his Mimi very happy!

Saturday, March 19, 2011

Jacob is back in the hospital after getting a transfusion yesterday. He was admitted last night with a high fever. Doctors aren't sure why yet. He is very weak from the chemo and will likely need another transfusion. So hard to see him so sick.

Sunday, March 13, 2011

Jacob is out of the hospital now. He's very quiet and not feeling very well. We were told to expect this, but he's always such a happy acting little guy, it's kind of hard to see him like this.

Friday, March 11, 2011

Prayers answered!! MIBG test came back. No cancer anywhere except the abdominal tumor we knew about and the new tumor by his kidneys. It's major wonderful that it isn't in his bones, bone marrow and lungs. The Power of Prayers. Thank you all! And the greatest thanks to God. The battle's not over but I am grateful for some good news. PS.. Chemo is doing a little rear kicking. He's really sick tonight.

Thursday, March 10, 2011

Jacob had a long day. X-rays and a 3 hour sedated nucleur test specific for Nuuroblastoma and then chemo. Again, he handles it like a champ. Sat up and ate a cheeseburger after all that!! He has everybody he meets up there charmed by his sweet smile and pure cuteness.

Wednesday, March 9, 2011

Day started with bad news. Drs said it was in his spine. Tons of tears and visit to my Pastor later, I got to the hospital and all thanks to God, we got good news. Tests came back and there's no cancer in his bone marrow and the lung fluid is negative for cancer! Dr said he thinks there is no spine cancer either after re-reading scans. We'll have to wait on one more test tomorrow for that. Our God is so Awesome!

It's begun.

Tuesday, March 8, 2011

Jacob just got back to his room. He had a 5 hour sedation to finish up all the scans. Papers are signed and the drugs have been ordered. At 8:00am the chemo begins and his life changes.

Monday, March 7, 2011

Jacob has surgery to remove bad port and put in the new port for chemo. He's doing well. Main doctors from Childrens Dallas just came in. Said there are multiple areas of tumors in abdomen. Said it is extremely important to start chemo immediately without waiting on tests. Shannon is going to call Sloan NYC in the morning. We need their direction, but main doctor is away this week. Lots of decisions!

Jacob's pneumonia turned out to be blood from tumor cells by his lung. The one small tumor that was to have been rfemoved is now a large one, with another by his kidneys. It's now full scale WAR on the cancer. AS soon as he is stabilized, we're off to NYC to begin a 2 year treatment plan.

Friday, March 4, 2011

Jacob is in the hospital with pneumonia. He's been trying to shake RSV for six weeks so he can have surgery, but it's settled in his lung. He's doing good. Just being Jacob - cool calm and collected. He still has major surgery ahead. We're waiting on a CT scan to check our that tumor. Please keep him in your prayers.

About Jacob

Jacob was a happy, healthy (according to his regular checkups), energetic 2 year old. Running around all day chasing after his 3 older sisters and getting into trouble like little boys should. I was a work from home mom with 4 great kids and all was right with the world. But on September 17, 2010, our nightmare began. Jacob was diagnosed with Stage IV High Risk Neuroblastoma. A rare, aggressive and deadly childhood cancer. Jake woke up that morning complaining that he hurt. I, thinking it was just pain from a little spill he had taken off his scooter the day before, redoctored a scrape on his knee and told him it would be better in a day or so. He seemed ok after that. But later that afternoon, just out of the blue, something told me to take another look at him. I laid him down on his back and starting at the top of his head began working my way down his body feeling for anything abnormal. Everything seemed to be alright until I got to his belly. I pressed down and initially didn't feel anything. But once again, something told me to press a little harder. So I did, and that's when I felt it. A hard spot deep in his abdomen towards the back of his body. Having no medical background I had no idea what it was but I did know that it should not be there. I called the doctor and insisted he be seen that day. At the office the doctor began to exam Jacob, he did not even have to say a word. I will never forget the look on his face when he said that he too thought he felt something there and that we needed to go immediately to Childrens and have some test done. 10 hours later my worst fear was confirmed. Jacob had several masses in his abdomen, on both adrenal glands, up in his chest and around his spine. Jacob had cancer known as Neuroblastoma. An 8 hour surgery was performed the next day to remove the massive tumors in his belly that were pressing on organs and causing his pain and a port was placed in his chest so his chemo could be delivered more efficiently. And although the surgeon was able to completely resect the tumors in his abdomen he had to close Jacob up with cancer still inside his little body. In a state of shock, I googled his disease looking for the place where Jacob would receive the absolute best care. The nightmare was just getting worse and worse with every word I read. Then I saw a website about a hospital in New York, Memorial Sloan Kettering, that was the world's leading Neuroblastoma hospital. There they have a world renowned Neuroblastoma surgeon, a true miracle worker, a team of world renowned Neuroblastoma doctors and treat more children with Neuroblastoma than any other hospital. I contacted Dr. Kushner at Sloan Kettering who got back with me right away. He listened as I told him about Jacob and told me that he thought he could help. I was now faced with a very difficult decision to make. There are also other amazing hospitals around the country that treat this disease but they treat it very differently than they do in New York. It was an almost impossible decision to make. There was no way of knowing which choice was the right one. I only had my instincts to go by and they kept telling me NY was the place he needed to be. So I decided to place Jacob in the hands of the doctors up there and we were on our way to NYC. Since being there Jacob has had 3 additional surgeries to remove tumors from both adrenal glands (one adrenal was removed completely the other partially) chest, pelvis, around his spine and to many lymph nodes to count. Jacob was treated with an agressive treatment plan which included 6 cycles of high dose chemotherapy, stem cell harvest and 14 doses of radiation. Sadly we received some discouraging news this past November. After his latest set of scans, Jacob's Neuroblastoma has been classified as Refractory. Meaning that it is not responding to the chemo any longer. The tumor in his spine is still there and possibly progressing. He has received 2 more cycles of chemo and hopefully at the end of February will start to receive the HU3f8 antibody. Although this is a very scary and upsetting setback, we will continue to battle on. Jacob and I will remain in New York at the Ronald McDonald House for the remainder of his treatment, leaving behind his three sisters, family and our home. Jacob's courage and sweet spirit throughout this whole ordeal has been an inspiration to all who know him.