The Prologue

Since Rohan cannot explain what is happening to him, I have decided to start this blog as way to translate to all of you how he is feeling and doing throughout his treatment for leukemia. I also want it to be a kind of record for Rohan when he is older and able to read. With that said, there may at times be postings that might not make sense to you but will make sense to him later.I hope this blog helps all of you who care about Rohan and us better understand the journey. I already know it will help me to have more clarity while I make this journey with him.

Sunday, September 28, 2008

We're Okay...I Guess

Well it's been a while since I wrote. Since we've come back home from the hospital, Rohan has been doing well. This second phase of treatment, Consolidation, is a bit easier. There are not as many medications at home and there are two weeks that we don't have to go to the hospital for chemo. But to ensure that we stay on our toes, Rohan's platelet count is quite high. Right now, there is nothing to do but monitor it. If it does get too high, though, there is the risk of blood clots. So if the counts get too high, they will prescribe that he take aspirin daily. Hopefully, this week's bloodwork will show that his platelets have gone down. It's amazing how many things the doctors keep in mind for each patient.

Otherwise, Rohan is doing fine. And so we are too. He is back to his cheerful and considerate self, and I'm glad to know that his despondent behavior was a temporary effect of the medication. We've been taking walks around the neigborhood and he is able to run quite a bit. I guess his energy is back up a bit. He does keep wondering why he has to continue taking medicine when he doesn't feel sick. We just keep reinforcing the message that the factory in his body that makes blood is broken in some places, and the medicine is fixing it. He doesn't really understand. But then neither do I...I don't understand why this had to happen to my vibrant boy.

Thanks to all of you for caring to read.

Monday, September 15, 2008

It's a Bumpy Ride

Luckily Rohan’s first month of treatment was unremarkable in that he did not get sick and need to be hospitalized. Unfortunately, that changed last week. On Thursday, he had a minor surgery to insert a more permanent port through which the doctors could draw blood and administer medication. The surgery went well, and we came home after having been at the hospital from six a.m. to 11:30 a.m. Two hours later we discover that Rohan has a fever. The doctor tells us we need to bring him to the hospital- so back we go again. And we end up having to stay there for at least five nights! His fever hovered between 102 and 104 for two days. The cause? A virus- most likely. “He has to be fever free for 24 hours before he can be released,” said the doctor. So we waited and prayed and entertained him and waited and prayed and entertained him.

We will most likely be home tomorrow, and Rohan will be better. Ravi and I will now be ever more vigilant in trying to minimize his exposure to any germs. It is a fine line between reasonable precaution and paranoid seclusion. I don’t think anyone would blame us right now if we lean toward the latter. It’s tough though. To tell your little boy that he can’t play with his friends or come to the grocery store with you or go out to eat or go to school is wrenching in its own way – even if you know it’s in his best interest.

Well folks, the journey continues…with all of its requisite ups and downs.

Friday, September 5, 2008

"Is solace anywhere more comforting than in the arms of a sister?"

This is my second post today, but I have been waiting to say this for some time now.

I'd like to introduce you all to my sister - Amisha. Now I know most of you know her, but I want you to see her the way we have. If you were with us this past month, you would have seen Amisha the Masi and Amisha the Sister (to both me and Ravi) and Amisha the Friend. All of these titles translate to Amisha -- the one who has helped bear the burden of our heartache like no one else.

She was basically living with us at the hospital and the first 10 days or so after we came home. Amisha is the only one besides me and Ravi that Rohan responds to all of the time. More importantly, he talks to her in a way that is unique and allows him to say things that he doesn't even say to me or Ravi. I think it's because she has let him know that she is here for him and him alone. He knows because she wakes up early to make banana pancakes with him. He knows it when she goes and buys supplies to do an art project together. Or because she simply sits and watches tv and eats ice-cream with him. Simply put, she allows him to be whoever he is in that moment. That essentially is what resonates with him.

What's amazing is that she has made me feel like she is here just for me. She's cried with me and encouraged me. Amisha has talked to people for me when I just couldn't. She has helped me clean up after the endless round of meals, fold laundry and gone shopping. It doesn't end there. Amisha has made sure I got out and relaxed a bit and kept my sanity. In short, she has been the pillar behind me ensuring that I didn't fall. Through this I have learned that there is almost no situation in which the presence of my sister does not offer some comfort to me.

She has talked to Ravi and kept him distracted with myriad topics of conversation. And she even managed to contact a friend of his to suggest she set-up a game of tennis with Ravi -trying to make sure he also got out and decompressed.

With all of that going on, she helped my parents take care of Arya. They have been watching her quite a bit lately. But she is a handful and a few hours with her can exhaust anyone. So sometimes when it was time for Rohan to take a nap, she would go over to our parents' to give them a break.

So I know many of you love her already. But now you know why for me the word seems to fall short of my meaning. We are bonded in a special way, and as odd it may sound, it makes me happy to know that Rohan is bonded to her in a special way as well. She was there in the delivery room when I was giving birth to him, and she has been there for him ever since. And for that he is lucky.

My Son

I miss Rohan - the boy I have seen him become over four years. I miss the Rohan who doesn't ever admit to being tired. I miss the all-star who will opt to play a sport, any sport, over almost all other activities. I miss the incessant talker, the optimist, the scheduler and the social busy bee. I miss the boy who seems at times to be reasonable beyond his age; the one who brought his compassion with him from another life; and the one whose smile is practically glued to his face. I miss my son! And even though I know that the changes in his personality are temporary and superficial, I just want to see him lob balls at the tennis court and hear him tell me that "When I get bigger and learn how to play golf then I will teach you and daddy. Okay? It's not too hard." We live with the hard facts of the disease and the treatment everyday, but sometimes the less tangible stuff is what causes the heart to break.

So on to the hard facts. Rohan completed his first month of treatment this week. I am relieved to say that his body responded to chemo well. He has less that .01% leukemia cells or 'minimal residual disease' in his body. So what does this mean? For one thing, he is off of the steroids for awhile (giving me hope that any day my son will be returned to me). Second, Rohan can move on to the next phase of treatment. We were waiting for the results of 'Day 29' since this journey began. And though I was anxious about it, I didn't realize how much until we got the good news. The sense of relief that he had overcome a big hurdle was deep.

Thanks to all of you for your prayers and support this past month and in the months to come.