Penny, the baby girl: Dillon

Showing posts with label Dillon. Show all posts

Friday, October 23, 2009

Question of the Day - Please answer!

I wish I had thought of this picture for Wordless Wednesday.

My question is, "WHAT DO YOU THINK PENNY IS SAYING TO DILLON?"

Tuesday, September 22, 2009

Prayers for Melissa

In about ten minutes, Melissa's back surgery will begin. I pray for a speedy recovery and let us also hope that your pain is elimanated!! I love you Mel! Get better soon.

UPDATE: Melissa had a quick surgery and was on the road to recovery by 11am. She did not react well to the anesthesia; however, she is still in great spirits!

Monday, July 13, 2009

Little Hearts Picnic Pictures

Our good friend Katie from the pediatric cardiology's office at CCMC. She touched both our children's lives!!

I wonder what Penny is laughing at?

Penny is always happy to play with her boyfriend Dillon!!

These kids are starting to look like some tired babies.

Tired babies after a fun day at the Strawberry festival in Unionville!

Wednesday, March 18, 2009

Go Dillon

Please pray for an uneventful surgery for Dillon and a quick recovery. He is have his g-tube placed today God willing. This will be huge for him!

Monday, February 16, 2009

Valentine's day Date

Penelope had a wonderful date with her boyfriend Dillon. He was a perfect gentleman to my little princess. I had a great time and enjoyed Melissa's good food and company.

Dillon had such a good time that he did not want us to even talk about leaving:

But we had to leave eventually to get the girl home and to bed. Don't worry Dillon we will see each other again really soon!

Thursday, January 22, 2009

Dillon update

I am such a bad friend. I told Mel I would post an update on her facebook wall last night but I feel asleep instead. Facebook acess is restricted here at work so if anyone else out there wants to write on her wall please do so. Dillon was brought to the hospital yesterday because after a few days of refusing to eat or drink he seemed ill again. They ran some blood tests to rule out some bad things, but his blood work came back normal today. Yay!!! They will let Dillon leave the hospital after they put in a G-tube or NG-tube. They are not sure which is best for him at this point. Melissa will need support either way because this is a tough time for her, but we all know that this will be the best thing for Dillon. Please pray that the doctors and Melissa are able to make the right decision and that Dillon feels better real soon.

btw, Penny is feeling better today

Tuesday, January 13, 2009

More Prayers for Dillon

I just got a voice mail from Dillon's mother that he is going back to the hospital to be admitted for his stomach problems and dehydration issues. It is very serious in that this little peanut cutie is acting very lethargic and he needs to be gaining weight, not losing it. Please pray that he will come out of it ok. Thank you!

Sunday, January 11, 2009

Penny and her boyfriend!

These photos are from awhile ago but I thought it would cheer up Dillon's mother because poor Dillon isn't feeling well. Here is Dillon and Penny together at the book party with Jessica as the consultant!

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Penelope's Story

After waiting the full 40 weeks for this bundle to arrive, I finally went into labor on Memorial day, 2007. At about midnight, I called my midwife's office. I was told to wait. At 2 am my contractions felt on top of each other and I called my midwife's office again. By the time my dear husband, Scott was ready (I had my bag and Nathaniel's bag packed previously) it was 3 am. We arrived at the hospital at 3:30 after dropping Nathaniel off at my mother's house. When I was checked, it was discovered I was already at 6 centimeters! My wish was for a natural delivery so Scott worked hard at rubbing my back and making me comfortable. Oh, yeah, and I worked hard too! At 4:45 am I was ready to push! I thought this part would be quick since my first child took about 30 minutes at this stage. However, this baby decided to take her time. At 6:30 am I was still pushing and my midwife, Mary, arrived just in time for the delivery. As she was gowning up I had to stifle my urge to push for a few moments and then before I knew it, Penelope Adara Ringrose came into this world at 6:51 am! Scott cut the umbilical cord as she laid on my abdomen.

It was a surprise that I had a baby girl, and I am glad I decided not to find out the sex. Another surprise we learned at birth was that Penelope had a little something extra, as in an extra 21st chromosone. I knew the second I saw her that she had Down syndrome, but I thought I could have been wrong. Then at 7:30 am, the acting pediatrician explained to Scott and me that our daughter had a lot of characteristics of Down syndrome. I couldn't believe that on this day that was supposed to be so joyous, I was receiving what I thought at the time was such devastating news. I didn't know much about Down syndrome. Scott and I were left alone to bond with her for a little while and then she was taken away at about 9 am to be checked over. The worst news was yet to come when we learned at 10 am that they suspected cardiac issues. The neonatalogist introduced himself and advised that Penelope could not maintain her blood oxygen saturation on her own and would have to be transfered to another hospital where she would need life-saving surgery. At CCMC (Connecticut Children's Medical Center), we learned that she has tetralogy of Fallot with pulmonary atresia (she is missing the pulmonary artery).

Her first surgery was on June 4, 2007 when she was just 6 days old. The surgeon had hoped to be able to do a full repair at this time, but Penny's anatomy did not enable this to happen. The surgeon was able to put in a Blalock-Taussing (or BT) shunt which kind of gives the blood a detour to the lungs so that it has a chance to be oxygenated. After 20 days total in the hospital, Penelope came home the day before she was 3 weeks old and was able to attend her brother's pre-school graduation.

She was scheduled to have her second surgery on November 27, but during triage at CCMC, it was determined that she had a pseudoanerysm on her right groin and the surgeon did not think it was safe to proceed. The pseudolanerysm resulted from a diagnostic catheter procedure that Penny had on November 14 to see if she was ready for another surgery.

We took our chances that she would be home for Christmas and had her surgery re-scheduled for Monday, December 17 . It was an uneventful surgery except that it was longer than we anticipated. We last saw her at 7:50 am and we did not hear news until a little after 4 pm. The breathing tube was taken out at about 2 pm the next day. Wednesday, the chest tubes were supposed to come out, but a pneumo thorax was found in the chest space and perhaps, leaving the chest tubes in was a better idea. One of the three tubes was removed on Thursday and we were able to begin feeding her from a bottle. Friday, the remaining chest tubes were removed and I was able to breast feed her again! Penny was doing so well she came home the next day and was indeed home in time for Christmas.

We all love her so much and can't imagine life without our beautiful baby girl.

Penny, the baby girl