Monday, August 23, 2010

Dearest Gift

Life. That would be life. It is the greatest gift and we are all here to help each other and protect life. Sometimes, with that gift comes heartache born into it. For our daughter, it was a succession of some heavy burdens, but also some incredible miracles leading up to her amazing growth and health. Our daughter was born exposed to Hepatitis B and C. She was born premature, anemic, with a slight heart murmur and of low birth weight. She later was discovered to have hydronephrosis of her kidneys and further on when we arrived to bring her home to our family, we discovered strabismus afflicting her eyes. Her beginnings were less than a stellar ideal place to start, but they gave her tools, knowledge, and experiences that she must learn in this life.

Amazingly, she is in the 75% range for height and weight on American charts. She has no signs of anemia, her heart murmur, and her exposure to the antibodies of her birthmother's Hepatitis B have not caused chronic HBV... she resolved that miraculously at around age 1. We have corrected her strabismus with surgery and she has had an amazing recovery and catching up with her cognitive, gross and fine motor skills, as when she was tested for teh school earlychild program, she is at 50% ready to go to Kindergarten and that was being in the country for less than a year!

When she came home at the age of 2 years and 2 months, I always kept hope that she did not have Hepatitis C, although her pediatrician said she really probably does because it had been more than 2 years and the maternal antibodies leave by that time. We did a simple blood test and confirmed the HCV. I was very nervous about the next doctor appt and post-poned it for a few months. I knew that HCV has many genotypes that determine how much harder or less hard the disease is to treat. Of course the hardest one is the most common to contract. I set up an appointment with the gastroenterolgist to get her RNA tested and to find out her genotype. I received the lab request but something told me to wait. The doctor said that they were not urgent tests so go ahead and wait 3 to 6 months so we didn't traumatize her any further.

Six months later, we go to the lab and as she sits wrapped in my arms, she starts whimpering about the impending blood draw, so I sat there singing to her in Mandarin, wiping tears from my eyes as her body tensed itself and sweated profusely so much that she went into slight shock from it all and started to drift to sleep. I had two phlebotomists assisting us who just happened to be Asian and I could see the tears start to well up in their eyes as well. One was an elderly man who quietly inquired, "Mandarin?" and I just nodded and kept singing. Even though we were behind a curtain, the entire place became silent as they listened. My nerves of singing didn't exist that day, because my daughter needed me more. My feelings were so heavy that day as I vowed that one day, she would be healthy no matter what it took.

I went and picked up the lab results the next day and read that her liver was very healthy, that indeed the HBV was completely gone, and strangely there was no genotype listed because they had to stop the test. That's okay, I said to myself, she will be having lots of these and we'll do it next time. Flu season hit and we didn't get a doctor appt for months to have the lab results read to us. Finally, it had really been pressing on me for weeks, even dreaming about it so I called the doctor's office and asked if they could ask him to read the results over the phone. He called about 5 minutes later, and the most serendipitous, sweetest words come out of his mouth, "She is negative. There is no sign of Hepatitis C. We have no idea why she doesn't have it, but rarely the maternal antibodies hang on longer than usual. That is why she didn't have a genotype." I was shaking and crying and overjoyed, almost speechless (which is highly unusual for me!) and because I kept stammering and asking questions about how it was even possible, he said we could retest in a year if we wish, because he must have thought I didn't believe him. May 4th is the day my world changed. My perspectives were given a jolt. I was ready for a long haul. My heart went out to all the people who are HIV, AIDS, HBV, HCV, HDV positive and so many other blood diseases, and who may never hear this kind of news, but today was our day to rejoice and they would want that.

I screamed and cheered when I got off the phone, ran and picked up Milana and gave her the most kisses she would allow (and maybe a few that she probably was like, Stop smoothering me! hee hee) and then gave huge bowls of ice cream to all the children. I called my husband and told him, who was of course in shock, and confused. Then he was upset because she was perfectly healthy and yet had to wait two years for her family. I told him that it was because she was meant for our family. I called family members excitedly and we all cheered, cried and overjoyed. All week, I would just think about the news and start to cry again. I get so giddy and happy everytime I think about it, months later. My gratitude cup is SOOOO full for her health. No parent wants their child to hurt.

I never never gave up hope that I would see this day of her being Hep C free, but I imagined I would be 50 or 60 and possibly have contracted it myself, making sure that she was taking care of. I resolved that I didn't care if I contracted it as long as I gave her a wonderful life. I still am amazed by this miracle. I didn't type this immediately; I was worried about saying it too often, like it would disappear as a morning dream. But it hasn't and it's real. I weep happy tears every time I think of it. The burden she unknowingly bore for months was a shared burden for me. Every time I look at nail-trimmers, toothbrushes, razors, band aids, those super-anti-viral wipes you see at the doctors, I pray and say Thank You. My children were taught to respect blood, that as much as it gives life, it can also take it away. That you must treat everyone's blood with sanitary hygiene practices. I have told them that blood requires gloves no matter whose it is because we want to preserve life.
I do want to say for all those who may consider adopting a child who has HCV; for day to day activities, they are like every other child. Unless they have an infection or reduced liver function, you can not tell any difference from one child to the next. Now, when HCV gets bad, it gets really bad, but children who contract it vertically (through childbirth) only have a 4 to 6% chance of keeping it past two years old (they just have the antibodies). If the HCv persists past then, it is considered chronic. The good news is that they have a higher chance of clearing it than adults and they often fair better with it. Little is known about children born with HCV because it is barely being discovered or researched. I have great hopes that in the near future they will have better medicines (like LDN helps the immune system naturally fight infections but there isn't enough funding to push for it to be approved for many illnesses it would help). You only monitor blood exposure and don't share personal hygiene items. They have so much love to give just like every other child and need every ounce of love back. Opening your heart to a child with HCV is an amazing journey. I would do it again in a heartbeat. If you have any questions about children who have HCV, please don't hesitate to contact me. I may be busy but I will answer. It is not a death sentence. Most people die with it, not from it.

Busted Lip

About a month ago, Milana was running in the mall and fell face first on the concrete floor. Four of her teeth went through the inside of her lip and blood just started gushing everywhere. I quickly asked the cashier girls to go get tissues. And they panicked and brought out band aids, wipes, papertowels, toys for the kids, a lei for Milana, a trashcan, some alcohol swabs, etc. One girl said, "I don't know how you are being so calm. I have an 18 month old and I don't know what I'm going to do when my child does this for the first time." I just smiled and laughed, "you get used to it and besides it's all relative." Relative, perspective... I knew that she was going to be ok. I checked her teeth and they didn't fall out or move, her lip was swollen as well as her face from crying, but she was healthy. A bumped lip was the least of what she has gone through. I didn't have gloves at that time and even if she had HCV, I wouldn't have cared, she is my baby girl and I love her with every ounce of my being. I'd give my life for her. Mommy loves you Milana and I'm so thankful you are here with us. Thank you for being my precious daughter.

Thursday, August 19, 2010

Cashews in the Washer

I am taking a break. Really. I have been pre-reading my anatomy book for class so that way when I am doing school for four children and myself, I'm ahead of the game. I'm on page 361 of a 560 page book. Finished my PSY class which was more like PSY year 3 not 101 (even a different professor said this teach went all out)... but I survived and hopefully wiser as well. School starts in one week and I am sorry but summer is way too long of a break; I favor year round schools... why? so many reasons, like doing daily homeschooling is exhausting while they're out (I give huge props to the full-time homeschoolers!!), adults don't have 3 month long breaks so why get the kids used to that and then throw them out into the work field and see if they can reverse 20+ years of summer break, and three, my ideas lag about the 2nd month on how to keep them entertained especially while reading about the sternocleidomastoid muscle while the kids are sneakily kicking each other and blaming the other child.

Oh wait, this was called "cashews in the washer"... why, because that is what I found when doing the wash after going to Legoland this summer. I put them in Kole's pocket when we went to the ocean to keep him eating and his mind off of... dun dun dun dun SAND ON HIS FEET! I had to pick out tons of them. I've had a multitude of oddities turn up in the washer but never cashews. What odd things have you found before? Haha... and you probably just thought I was nuts naming this post about nuts! har har I need sleep.

I also found that Milana LOVES rollercoasters and other exciting rides... not too keen on the darker ride that strolls through cave-like interiors. Kole... not a thrill seeker; loves laser shooting rides. Jadyn half and half and Kole's nerves seem to overtake her sometimes, but Nika and Milana's adventurous spirits sometimes win out... Nika mostly there and while she'll go on any ride, she gets nervous just before take-off. I don't have nerves other than wishing I didn't have to rub my neck after the inevitable whiplash of the bruisers. The kids are so adorable and loved having some time to chill.

We also went to Arizona in June for a week and a half. My niece's wedding gave us a great reason to visit everyone. It was right in the middle of my PSY class so I did 4 wks of college work in two weeks (which since it was a summer class was equivalent to 6-8 weeks) just so I could go and enjoy AZ (I think I still am having dreams about seratonin re-uptake!). We went swimming, visited a small amusement park, had a great pot-luck with my giant familia (which some of them had never met Milana before so that was actually very nice as Milana really liked them... I waited for her to be freaked out by their sheer voluminous numbers but she did awesome), and my kids went on a boat for the first time ever... I even wake-boarded and didn't get dragged the whole time.