Happy Halloween!

I hope everyone had a great Halloween! We sure did!! The kids had so much fun, Alexis was a Fifties Girl, Kayden was a Vampire, Tavion was Superman, & my niece Lyndsee was a werewolf. We stayed out for about two and a half hours so they all got a ton of candy. Kayden hasn't felt good lately, he's been coughing terribly and weezing so I had him bundled up on top of his costume. He got tired before the other kids so he went to the car with my sister and brother in law. It makes me so sad sometimes when I see him try to keep up with Alexis & the other kids but he gets worn out so easily, plus he stays sick anymore. I just hope next year we'll have the sickness behind us and if the doctors plan on during surgery it'll be done and he'll be fairly well recovered by then. So here we are almost November, it seems like this year has went by so fast, so much has happened good and bad. I just hope they last couple of months go smoother than I think they will, I hope the holidays are good mostly for Kayden if he's sick or if he has surgery before them, he deserves the best. He's been through so much it makes my heart break. All we can do is pray that God will keep us all safe & help my son get better.

Kayden's Story

Kayden was born on December 21, 2007 at 1:24 a.m. He was born with a bilateral cleft lip and palate, Dilated Cardiomyopathy, and what was thought to be Ebstein's Anomaly. He stayed in the NICU for 2 weeks after birth, he was on oxygen for the first couple days of his life. At a month old, Kayden wouldn't keep his formula down of course I worried, so we ended up at the ER that night to figure out what was wrong. The doctors had no idea, finally they admitted him into the hospital and early the next morning they did an ultrasound on his tummy. He had pyloric stenosis, which if you don't what it is it's a hole that helps your food digest and go through to your stomach, his was too small so they had to do surgery to make the hole bigger. He did well through the surgery, of course I worried the whole time he was in the OR. Anyways Kayden had a lip adhesion done in April 2008 at 4 months old, this was the first step to repair his cleft lip/palate. In October 2008, at 10 months old he had surgery to complete the lip repair. He did great I was so proud of him, it was emotional because he looked so much different but he was still my beautiful little baby boy. In January 2009, Kayden had the final surgery in repairing the cleft, this one was on his palate, he did great although it took a little bit longer than expected. It was very sad to see after the surgery because his lips were so swollen and he had a stitch in his tongue to hold it down and not touch his palate. Kayden went all through 2009 without any problems, his heart had gotten alot better, not all the way but where we didn't have to worry so much. In about August or September I noticed he had a bump beside his ear that was red and it felt like a cyst or something, I wasn't sure so I took him to his pediatrician to find out what it was. He did notice that Kayden had a preauricular pit on his ear and the bump was close to it, so he said he thought the cyst was coming from the pit but wanted an ultrasound done to be sure that's what it was. Sure enough the cyst was coming from the pit so therefore they said it was a preauricular cyst. He was put on antibiotics to try to get it to go away or the infection in it to go away. It just got worse, so we started going to an ENT to try and get it to go away, they also said once the infection stopped flaring up surgery would be needed to remove the cyst. After months and months of fighting this thing, he had surgery in June 2010 to remove the cyst, he had ear infections all month in June(these were the first time since birth he had ear infections) and a cold that was on and off all month. His ENT doctor knew this but still felt it was necessary to go on with the surgery. After that things went pretty much downhill, he slowly lost his appetite, started sleeping more than he usually did which is alot because he's always loved to sleep, then I noticed his legs and feet started swelling, every morning he started waking up and his lips, hands and feet would have a blueish color to them. I took him to his pediatrician to find out what was going on with him, he had no life to him he laid around, slept, didn't eat & was swelling. The pediatrician noticed his liver was very swollen which worried him he felt that blood could be backing up in his liver and his heart wasn't pumping the blood like it should have been, Kayden had an appointment the following week with his cardiologist but his pediatrician got the appointment moved to the next day. We went in for the appointment I was not expecting what happened that day. They did an echo on him and his heart function had got so much worse, the tricuspid valve was leaking more now and it was just terrible. His cardiologist then told me on July 28, 2010 that Kayden was in Congestive Heart Failure. Those three words I did NOT want to hear, my grandpa died from CHF so I was so scared, I didn't know what to do, I didn't know if I should cry if I should scream I just didn't know. So his cardiologist told us to go get chest x-rays and go straight to the hospital up to the PICU, so that's exactly what we did. We were transported to the University of Virginia Children's Hospital the following day, which we were there for a little over a week. Kayden's since been going to his cardiologist every 2 weeks to increase one of the new medications they put him on. His lungs are clear but he still hasn't acted like himself since June. He still mostly lays around and doesn't eat much. He has no swelling since he is on Lasix now that's keeping the fluid from building up anywhere. I took him to the cardiologist on October 25 because I was so worried he slept the day before all day he was awake for about 3 hours the whole entire day, didn't eat & laid on the couch when he was awake. So the cardiologist noticed the Tricuspid valve leaking very badly and was concerned & thinks we should think about replacing the valve. So here we are and on November 9 Kayden goes for some diagnostic tests which they will put a catheter in his heart to see if the left side is affecting the right side, measure the pressure in his lungs, as well as any other information they need. If his left side is affecting the right then he will be too high risk to do anything with the valve, so I'm not sure at this point what the option would be, but if it is not affecting it then they will be most likely replacing his tricuspid valve. This is what I have feared since I found out about Kayden's heart which was at about 4 months pregnant. I still don't know what to think or expect. I'm worried & I'm scared. So this is the way I know of to get my feelings and thoughts out and to keep people updated on him. Also I want people to be MORE aware of Congenital Heart Defects, they affect so many kids each year. And when you think it's only 1 heart that's broken it's actually breaking many more, including moms, dads, brothers, sister, grandparents, aunts, uncles, etc.


UPDATE on Kayden's story ( May 2011)..Kayden had his first open heart surgery on March 17, 2011. They did the glenn & a cone repair which is repairing the tricuspid valve. His valve is now moderately leaking so he will probably have another surgery. The cardiologists have now classified his case as a dysplastic tricuspid valve with tricuspid regurgitation instead of Ebstein's. He is doing well with the exception of having a pleural effusion about 3 1/2 weeks out of surgery. And here we are going on 2 months after surgery & the effusion is coming back. Hopefully this will get under control soon. He still isn't very active like he use to be before his heart got worse, but I'm getting better with accepting that he will probably never be that child again. I just have to cherish the memories of Kayden while he was well.


Update on Kayden: 
On June 14, Kayden went to UVA his heart kept getting worse after the effusion. So UVA did an echo and his heart was actually worse than before the surgery in Boston, they said the only reason things weren't worse than what they were is because of the Glenn he had done in Boston. So the plan was to do a transplant evaluation and get him listed asap. They did everything to list him, the cath knocked him down though. It threw him under the bus pretty much. His heart rate dropped in the cath lab, they got him stable and back upstairs where they were having blood pressure issues I believe it was. Well he stayed intubated for about a week and he came off the vent. While they were getting him off that, he was saying 'no more no more no more', those were the last actual words we heard Kayden say. He took a 2 hour nap and woke up completely out of it. He was having uncontrollable movements, he wasn't talking and he kept looking around the room. I had never seen him do this so I was worried, they did a ct scan and nothing showed up. According to them it was medications and to this day I will swear up and down to any damn doctor it was not no effin medications. He finally got the movements under control. But he wouldn't talk, I would whisper things to him and if he'd come out of it for a second he would shake his head and one time he mouthed 'love you' to me. Kayden passed away July 14, 2011 he was on the transplant list for 2 weeks. I feel like they waited too long to help my baby. I am a firm believer in everything happens for a reason but I can't figure this one out. I also know Kayden is in a better place he is no longer hurting but damn it I just want him back I miss him and want to hold him. He was and will always be my little miracle <3