Wednesday, October 22, 2008

Yesterday was our last visit with our Dr. at Hunterdon. It was a little sad. We have been seeing them for twice a week for the past two months. They have seen me at my best and worst. They all have been so wonderful to me and my husband. They will be missed.
The appointment went well. Sydney cooperated for them so they did need to chase her with the heart monitor like usual ( she has quite the reputation in the office). Her Bio-physical looks great and mommies blood pressure went down. So all went well. We go to CHOP on fri. I hope they will beable to give us a date. I am hopeing for the week of Nov. 10 ( 37 weeks.). Lets keep our fingers crossed. I will keep you posted.


theparkerreesefoundation said...

I found your blog tonight and wanted to let you know that we are praying for Sydney and your family.

Our daughter, Parker Reese, was born with CDH on May 7, 2006. She lived 20 amazing hours.

If there is anything we can do please let us know.

You will remain in our thoughts and prayers.

Fer said...

I founded your blog on Nayeli's blog. Just wanted to let you know that we are praying for Sydney.
Mexican Rep. for Cherubs

Dawn T. said...

Saying tons and tons of prayers for you!!! Please know that CHERUBS is here to help you in any way possible. We are a huge (2250+ CDH families) international organization here to help support families, supply CDH information and research CDH. Our members would be happy to listen, answer questions, share their stories and offer you support.

I also want to let you know that there is a new CDH blog ring for families affected by Congenital Diaphragmatic Hernia.

This is a service to all CDH families to help us keep up with CDH blogs and to support and encourage families that need it. You can view it on our blogger blog at

As you can see, it does not list CHERUBS or any CDH group and it is free to join. You can click on Previous and Next and surf from CDH blog to CDH blog.

You can add it to any blog - myspace, blogger, wordpress, live, etc. Make sure to add your CHERUBS site blog to this as well!

To join, go here:

I hope you have a wonderful weekend!

President & Founder, CHERUBS
mom of Shane (1/28/93-9/11/99), LCDH x6, vent 1.5 yrs, oxygen 2 yrs, trach 2 yrs, Mic-Key feeding button, deaf 6 yrs, sight impaired, ASD, pulmonary sequestration, hypospadius, recurrent pneumonia and blood infections, hospitalized off and on his entire life, lost to gastropleural fistula - loved matchbox cars, Sesame Street and books, walked, signed, was a happy little guy!

Tracy Meats said...

I found your blog again through CHERUBS and a prayer request for Sydney. Praying for Sydney in the weeks to come. If you ever need to talk, have questions, want to share Sydney's journey--CHERUBS is here for you. You are not alone and there are so many people that want to see Sydney win her CDH battle.

Tracy Meats - mom to Ian(born with a LCDH on 4/3/04) and WY and CO State Rep. for CHERUBS

Shawn said...


Sydney is now featured on Cloud Nyne Design. Thank you for allowing us to follow your journey.

Shawn C
Cloud Nyne Design

Kathi Krablin said...

Kathy: We are delighted to hear that Sydney has arrived - we can't wait to meet her and to tell her what an amazing family she has. She's beautiful in her pictures. We are sending our prayers for you and Gary and the kids (and Jim and Sheila too, of course).
Much love,
Kathi and Bill

Liz and Shane Nelson said...


we are thinking of you and praying for Sydney.

casau said...

she's here??? oh do tell us all about here soon!! prayers for all of you guys!!!