Our friends Matt and Jamie Wallace, who lost their daughter Nevaeh back in April, have come up with a beautiful way to honor her and keep her memory alive.
Playroom of Hope is a room that is in the new building at Children's Hospital. It is currently being used as offices but as soon as the money is raised, it will be turned into a room for the kids in the hospital and their siblings to go and hang out. Please consider giving to this most worthy cause.
Remember them in your prayers as well. They do have a CaringBridge Website that Matt continues to update to help in the healing process.
Thank you,
Jodi
Showing posts with label Nevaeh. Show all posts
Showing posts with label Nevaeh. Show all posts
Thursday, August 27, 2009
Sunday, April 26, 2009
Heavy Heart
It is with a heavy heart that I am writing this.
Our friends Matt and Jamie lost their beautiful 14 month old girl Nevaeh today. She was born with a heart defect and was doing so well. Tuesday she was admitted to the hospital. They were hoping it was just a virus but later learned that she was in heart failure.
They had started her on some medication hoping that her heart would recover some of the function. The doctors released her and were planning on watching her closely hoping she would be able to qualify for her 3rd heart surgery.
From what I have heard, she was at home with Jamie this morning when she stopped breathing and was taken by ambulance to the hospital where they tried to resuscitate her. Matt and Jamie asked them to stop after an hour. They were able to spend some time holding her afterwards.
We were all praying for God to heal her heart and He did. I just wish He did not have to take her home to do it.
Please take a moment to pray for this sweet family. They do have a CaringBridge website if you feel led to leave them a message.
Nevaeh
God Bless,
Jodi
Our friends Matt and Jamie lost their beautiful 14 month old girl Nevaeh today. She was born with a heart defect and was doing so well. Tuesday she was admitted to the hospital. They were hoping it was just a virus but later learned that she was in heart failure.
They had started her on some medication hoping that her heart would recover some of the function. The doctors released her and were planning on watching her closely hoping she would be able to qualify for her 3rd heart surgery.
From what I have heard, she was at home with Jamie this morning when she stopped breathing and was taken by ambulance to the hospital where they tried to resuscitate her. Matt and Jamie asked them to stop after an hour. They were able to spend some time holding her afterwards.
We were all praying for God to heal her heart and He did. I just wish He did not have to take her home to do it.
Please take a moment to pray for this sweet family. They do have a CaringBridge website if you feel led to leave them a message.
Nevaeh
God Bless,
Jodi
Saturday, February 14, 2009
Happy Valentine's Day, Happy Birthday!
I would like to wish a few people Happy Birthday today.
My mom
Nevaeh
My cousin
It is a super special day for Nevaeh as it is her first birthday. It is amazing to see this little girl grow and change all the time. She was born withHLHS but you would never know it. You can keep up with her progress here. We hope you have a great time at your party and we wish we could be there!
Emma is doing very well. There was no obstruction in her bowels, which is an answer to prayers. She was just constipated, but not after the study, it cleaned her out quite well. All over her clothes and my pants. Oh well, not the first time and it won't be the last!
I ended up having shingles. I went to the doctor on Monday for the lump in my neck and he did some blood work to rule out anything with the lymph nodes. He figured it may be related to my neurofibromatosis. Tuesday I got a rash on my chin so I just put some cream on it, but Thursday morning it was all blistered so I went back to the doctor and he said it was shingles. I got some medicine and the rash is better now, but I still have some pain, though that is getting better too.
Have a great day!
God Bless,
Jodi
My mom
Nevaeh
My cousin
It is a super special day for Nevaeh as it is her first birthday. It is amazing to see this little girl grow and change all the time. She was born withHLHS but you would never know it. You can keep up with her progress here. We hope you have a great time at your party and we wish we could be there!
Emma is doing very well. There was no obstruction in her bowels, which is an answer to prayers. She was just constipated, but not after the study, it cleaned her out quite well. All over her clothes and my pants. Oh well, not the first time and it won't be the last!
I ended up having shingles. I went to the doctor on Monday for the lump in my neck and he did some blood work to rule out anything with the lymph nodes. He figured it may be related to my neurofibromatosis. Tuesday I got a rash on my chin so I just put some cream on it, but Thursday morning it was all blistered so I went back to the doctor and he said it was shingles. I got some medicine and the rash is better now, but I still have some pain, though that is getting better too.
Have a great day!
God Bless,
Jodi
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