chelleydi77
Mouseketeer
- Joined
- Mar 5, 2011
- Messages
- 228
Hi everyone! My oldest daughter is the newest Wish Kid from San Diego. We met with her wish granters yesterday and she wished to "dream on the Disney Dream". They are looking at dates in July or August for us to take a 5 day/4 night cruise to the Bahamas! We are so thankful for the MAW foundation and all they do!
A little background on our Wish Kid. When I was pregnant with her we noticed her heart rate was extremely low (80s or lower). We did testing (amnios, genetic screenings, etc) and after months of not knowing anything, discovered what she has is a complete heart block (the nerves of the top of the heart did not connect with the nerves from the bottom of the heart. The top beats normally, the bottom beats as it wishes). After she was born she was observed in the NICU for 5 days and seemed to be doing okay.
When she was 20 months, she had to have her PDA coiled and they discovered the pressure in her heart was dangerously high and decided to do the pacemaker asap. She's done fairly well with her pacemaker other than being limited to what activities she can do. She's had this pacemaker for 6 1/2 years and will have surgery in June to replace it.
Madison has a younger sister that is completely heart healthy (thank goodness). Apparently after having one child with this issues, the chances of having another is fairly high.
Thanks for reading and for "travelling" with us as we prepare for our trip!
A little background on our Wish Kid. When I was pregnant with her we noticed her heart rate was extremely low (80s or lower). We did testing (amnios, genetic screenings, etc) and after months of not knowing anything, discovered what she has is a complete heart block (the nerves of the top of the heart did not connect with the nerves from the bottom of the heart. The top beats normally, the bottom beats as it wishes). After she was born she was observed in the NICU for 5 days and seemed to be doing okay.
When she was 20 months, she had to have her PDA coiled and they discovered the pressure in her heart was dangerously high and decided to do the pacemaker asap. She's done fairly well with her pacemaker other than being limited to what activities she can do. She's had this pacemaker for 6 1/2 years and will have surgery in June to replace it.
Madison has a younger sister that is completely heart healthy (thank goodness). Apparently after having one child with this issues, the chances of having another is fairly high.
Thanks for reading and for "travelling" with us as we prepare for our trip!