Kamryn Hope's CDH Blog

About our family

Shawn, Stephanie, Hollie, Brooke, and Kamryn live in McKinney, Texas. We have battled infertility problems throughout our marriage, but after numerous IVF attempts we were blessed with Hollie 7 years ago through a frozen embryo transfer (FET). Since her birth in 2002, we attempted numerous IVF procedures trying to once again become pregnant. After numerous failed attempts, we found out in October 2008 that we were finally successful. To our surprise, two of the three embryos we transferred implanted and we were going to be the proud parents of Kamryn Hope and Brooke Ashlyn. Our absolute joy turned to fear and confusion at 13 weeks when it was discovered one of the twins, Kamryn, had a congenital diaphragmatic hernia (CDH). We hope this blog not only allows our family and friends to share the joys of Kamryn and Brooke, but also the struggles we faced as Kamryn battled and overcame her CDH condition.
Shawn, Stephanie, Hollie, Brooke, and Kamryn
Stephanie: email
Shawn: email

History of Appt's

12/11 - 1st OB appt (10wks)
12/29 - NT Sono-Possible CDH (13wks)
1/8 - OB appt (15wks)
1/21 -CDH Confirmed Sono (17wks)
2/5 - OB appt (18wks)
2/12 - Amnio/Ped. Cardiologist (19wks)
3/05 - Hi-risk OB appt (22wks)
3/11 - OB appt (23wks)
3/20 - Children's Houston Consult (24wks)
3/26 - Hi-risk OB appt (25wks)
4/2 - OB appt (26wks)
4/3 - Children's Dallas Consult (26wks)
4/16 - Hi-risk OB appt (28wks)
4/17 - OB appt (28wks)
4/24 - Pediatric Cardiologist (29wks)
4/29 - OB appt (30wks)
5/7 - Hi-risk OB appt (31wks)
5/11 - OB appt (31wks)
5/20 - Hi-risk OB appt (33wks)
5/21 - 2nd MRI
5/27 - OB appt (34wks)
6/2 - Hi-risk OB appt (34wks)
6/8 - Admitted to Parkland Hospital (35wks)
6/17 - Delivery of twins (37wks)

Just wanted to touch base out there and post a few pics of the girls. Kamryn has made a 100% complete recovery, and is my little firecracker as usual! She is very vocal and opinionated, but she's still a mama's girl. Brooke, is pretty quiet and reserved, but has no problem meeting new people. Hollie is about to finish 4th grade. I can't believe she's about to be a 5th grader. She's very active in Softball and Volleyball. She's going to have a busy summer this year with camps, etc. I'm also going to get the twins in gymnastics this Summer. I can't wait. They will love it. Here are a few pics....

Kamryn

Kamryn swimming

New big girl beds!

Trip to Kingsland last weekend

Hollie

Easter 2012

Brooke swimming

I also wanted to bring your attention to a new CDH baby to be born soon in Dallas. The parents names are Casey and James. Their baby's name is Wyatt. They contacted us last night thanks to Dr. Zaretsky, which prompted me to update our blog a little bit. Anyway, Casey is due in about 2 months, and naturally scared! Please pray for this sweet family. Pray for no ECMO! Pray for liver to be down. Pray for healing! Pray for understanding for the parents. Pray for the doctors! Pray for God's will! Here is a link to their blog. So sweet! http://familydavises.blogspot.com/

I'm so sorry that I've been so bad about updating our blog. The girls have been keeping me busy. We are going non stop all the time. They are going to be turning 3 in 2 weeks. So hard to believe. You better believe I will post pictures from their party. We will be throwing it down!!!

That's all for now. Much love to all of you!

Stephanie

CDH Overview

Congenital diaphragmatic hernia (CDH) refers to a defect in the diaphragm that allows the abdominal organs (stomach, intestine, liver, bowel, and spleen) to migrate into the chest cavity in utero. Diaphragmatic hernia results by the failure of the diaphragm to close or to form at approximately eight weeks’ gestation. This migration of organs into the chest cavity, through the hernia, prevents the lungs from developing properly due to crowding and compression. Babies who have CDH suffer from small and underdeveloped lungs. This condition is referred to as pulmonary hypoplasia. Although hypoplastic lungs are the underlying threat to survival, the critical nature of the condition at birth is due to pulmonary hypertension or persistent pulmonary hypertension in newborns (PPHN) as a result of the underdeveloped lungs. Since this condition will be present “at birth”, it is referred to as Congenital Diaphragmatic Hernia as opposed to Diaphragmatic Hernia. CDH is known to occur in 1 out of every 3000 live births and currently has an average survival rate of 50%.

Our Medical Team

This is the medical staff committed to winning this battle:

Parkland/Children's of Dallas Fetal Program - Outstanding option for CDH care. The medical staff exceeded all of our expectations. If you are interested in a consultation, please email me for information.

Michael Zaretsky, M.D. - Dr. Zaretsky found the abnormality during our NT scan at 13 weeks. He has been a true blessing in guiding us through every step of this situation and coordinating all of our care. When we are lost, unsure, or just scared, this is the Doctor we turn to and place our trust in. He has put together a rock solid team with Leah and Sharon and we would be lost without them!
Courtney G Trylovich, M.D.- Dr. Trylovich is a wonderful OB and her staff is fantastic! LOVE HER! She is such a caring and compassionate Dr. that truly takes so much time with us at each visit. If you live in Dallas and want the best OB/GYN available, look no further than Dr. Trylovich!
Michael Day, M.D. - Dr. Day is our Pediatric Cardiologist and he is fantastic. He honestly would have spent all night with us answering questions. He was so thorough and genuinely cared that we walked out of there with everything we needed. We really can't say enough about the care we received from him and his staff.
Rashmin Savani, M.D. - Dr. Savani has been nothing short of amazing and we truly believe he has taken a personal interest in our care. Feeling like you have an advocate during this journey is priceless and he has done more for us than we could have hoped for. He is committed to doing what is right, improving care, treating patients with the utmost respect, and at the same time will shoot you straight on what's going on in the most compassionate way. What more could we ask for!
Diane M. Twickler, M.D. - Dr. Twickler's reputation in fetal imaging is remarkable and we feel incredibly fortunate to have her handling our MRI tests and interpreting the findings. She has been involved with a number of studies on CDH which I am sure helps in her ability to be so thorough with us on what she sees. She got it right when other centers were off the mark in our case. She is a wonderful person that knows fetal imaging better than most in my opinion.
Myra Wyckoff, M.D. - Dr. Wyckoff is one of the Neonatologists in the Parkland NNICU and although she was not Kamryn's primary doctor, she is nothing short of outstanding. Dr. Wyckoff is no nonsense and displays a desire and expectation to win everyday. Observing her during rounds, she is an outstanding educator to the staff. Her communication with us was always direct, honest, and to the point. Anytime we spoke with her, we left better informed and never confused. I would want her taking care of my child anytime and are just beyond impressed with her.
Stephen Megison, M.D. - Dr. Megison was responsible for fixing Kamryn's hernia and we could not be more pleased with every aspect of that experience. Dr. Megison is a great communicator, both before and after surgery and his work was nothing short of impressive. It doesn't appear that Kamryn will have any reflux issues and all her internal processes work normally. I firmly believe this is because of the care that he took during the procedure. Another positive is her scar which is almost not noticeable. Taking care to minimize this scar was important to us and he did an amazing job. He is very well respected and recommended by his peers and if any of my children need future surgery, he will be our first choice.
Parkland NNICU Nursing Staff - The nursing staff at Parkland are amazing and the ones we truly believe not only saved Kamryn's life, but expedited her recovery. The team in general was outstanding. Our four primary nurses are without a doubt what pulled us and Kamryn through this experience. Traci, Monica, Tamara, and Gretchen were our advocates, friends, and voice of reason each and everyday. They are gifted nurses that cared for our daughter as if she was their own. They genuinely exceeded our expectations everyday. We can't adequately express our gratitude, but we hope they know they are our heroes!

5 comments:

The Cole's June 6, 2012 at 5:56 AM: Thanks for the update, glad you are all doing so well!
wreeves June 28, 2012 at 12:58 PM: I tried finding a "contact me" button on your blog but couldnt find it. So I thought I would comment first. My name is Whitney and I am 24 weeks pregnant. At 21 weeks my baby girl was diagnosed with CDH. I live 11 hours from Houston but feel like thats where I need to be. I read that your baby was treated there and was wondering if you would be willing to talk to me about that. My email is whitneyreeves@hotmail.com if you would like to email me. I would really appreciate any information.
Thank you!

http://sunnisstory.blogspot.com/
The Griffin Family October 13, 2012 at 12:15 AM: Hi old friends... I haven't looked at the blog world in so very long. I am grateful your whole family is well! I was surprised to see that Kamryn re herniated! So glad she is doing okay now. Our Max reherniated as well, at 13 mos old! All the rare occurrences head our way, right?!

Makes me happy to see their smiling faces.

Claire griffin
Bridal saree June 12, 2013 at 1:10 AM: i do pretty much the exact same thing, local vhosts and all. taking nightly backups of /home is easy with rsync, so when anything goes awry, i just pull down the folder from my vps. since the cronjob itself is in the folder, even my backup script gets backed up. what ide do you use?
Unknown December 24, 2015 at 9:50 AM: Further useful article in again with another great article source Obat Hernia

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>> Tuesday, May 29, 2012

5 comments:

Kamryn makes the local news (7/31/09)

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