I feel like I know so much about you. You are a courageous young woman. My son passed away from Hypoplastic Left Heart Syndrome, and my niece has the same condition and just got extubated Sunday. I know you are getting a heart. I was up in the PICU today and Brytt told me the great news! We are praying for you and your family. Get well so you can get home and experience the good things of being a teenager! Heart hugs and prayers, Emily and Mike Gourley parents to angels Lilly and Ryker
Megan, Congratulations on your new heart!! My son Joseph got his new heart in January and life has never been better for him. He is 14 almost 15 and it is great to be a normal teenager. I hope your new heart works as well as his does and that you can soon go home. You can view Joseph's blog at www.heartransplant.blogspot.com - it may help pass the time. Get well soon but remember to be patient with your body as it goes through recovery.
It was so good to meet you and your Mom on Thursday. I just read the news that you are right now getting your heart - we are so happy for you. We are praying that all goes well for you! Carter wasn't with me when I met you but if you would like to read about him you can view his blog at http://andersons6175.blogspot.com
We will keep updated on you through your blog!
Hugs Kristi, Alan, Parker, Ashleigh and Carter Anderson
Megan, It was so wonderful to get to meet you last week. Bryt has told me so much about you. I am so happy that you got your new heart. I hope that your recovery goes smoothly and that you will be able to regain your strength quickly. You have been given such a wonderful gift! Lots of love, Hollie (and Elaina too!) http://hollie-walkingthefineline.blogspot.com
I didn't get to offically meet you, but my son Rhett was in the hospital for back surgery last week. I heard all about you from some friends that we have up there.
Now that I see your pictures I realized I saw you down in the Rainbow Cafe too. I wish I would have known it was you. You are an amazing ispiration to all of us.
Rhett had open heart surgery when he was 4 months old, and still has some issues but he is doing well overall. He has Down Syndrome just like Carter.
When you feel better if you want to read about him our blog address is http://rhettsjourney.blogspot.com/
We are praying for you, and want you to know that we will be cheering you on through your recovery.
Megan we just want you to know that so many people out there are cheering for you and praying for you. We are so glad that you go a new heart. Way to go sweetie. We look forward to the post that says you are on your way home.
Hi Megan, my name is also Megan. I am the mother of a heart baby. My daughter Isabella has had two open heart surgeries. You are an amazing young girl. Love and Prayers Megan
My Name Is Megan, Im A CNA And 21 Years Old. I received a heart transplant in September of 2008. My new heart has given me a new chance at life and I am forever grateful to the family that gave me my "Angel Heart Thumper". Today I am 19 years old and awaiting a second heart transplant due to severe Coronary Artery Disease.
Know In 2013, I'm In Treatment For My Eating Disorder At Age 19 To Present. I'm Going To Get Healthy So I Can Recive A Secound Heart Transplant.
If you would like to make a Donation for me. How to help
The Megan Birk Heart for Life supplementary trust fund is set up for Megan Birk at The Village Bank, which has multiple locations in St. George.
Thank You Very Much.
8 comments:
I feel like I know so much about you. You are a courageous young woman. My son passed away from Hypoplastic Left Heart Syndrome, and my niece has the same condition and just got extubated Sunday. I know you are getting a heart. I was up in the PICU today and Brytt told me the great news! We are praying for you and your family. Get well so you can get home and experience the good things of being a teenager!
Heart hugs and prayers,
Emily and Mike Gourley
parents to angels Lilly and Ryker
Megan, Congratulations on your new heart!! My son Joseph got his new heart in January and life has never been better for him. He is 14 almost 15 and it is great to be a normal teenager. I hope your new heart works as well as his does and that you can soon go home. You can view Joseph's blog at www.heartransplant.blogspot.com - it may help pass the time. Get well soon but remember to be patient with your body as it goes through recovery.
Megan,
It was so good to meet you and your Mom on Thursday. I just read the news that you are right now getting your heart - we are so happy for you. We are praying that all goes well for you! Carter wasn't with me when I met you but if you would like to read about him you can view his blog at http://andersons6175.blogspot.com
We will keep updated on you through your blog!
Hugs
Kristi, Alan, Parker, Ashleigh and Carter Anderson
Megan,
It was so wonderful to get to meet you last week. Bryt has told me so much about you. I am so happy that you got your new heart. I hope that your recovery goes smoothly and that you will be able to regain your strength quickly. You have been given such a wonderful gift!
Lots of love,
Hollie (and Elaina too!)
http://hollie-walkingthefineline.blogspot.com
Megan,
I didn't get to offically meet you, but my son Rhett was in the hospital for back surgery last week. I heard all about you from some friends that we have up there.
Now that I see your pictures I realized I saw you down in the Rainbow Cafe too. I wish I would have known it was you. You are an amazing ispiration to all of us.
Rhett had open heart surgery when he was 4 months old, and still has some issues but he is doing well overall. He has Down Syndrome just like Carter.
When you feel better if you want to read about him our blog address is http://rhettsjourney.blogspot.com/
We are praying for you, and want you to know that we will be cheering you on through your recovery.
Sending lots of hugs from Rhett and I!!
Pam and Rhett
Megan, this is Gracey's aunt. I want to tell you that my entire extended family has been praying for you and checking your blog for updates!!
It will be wonderful to hear from you when you are feeling well enough to write again.
We hope that your new heart is pumping away as wonderfully as possible!! I'm so happy that you've been given another chance for a full life.
Organ donation is a miracle!!
Megan we just want you to know that so many people out there are cheering for you and praying for you. We are so glad that you go a new heart. Way to go sweetie. We look forward to the post that says you are on your way home.
Hi Megan, my name is also Megan. I am the mother of a heart baby. My daughter Isabella has had two open heart surgeries. You are an amazing young girl.
Love and Prayers
Megan
Post a Comment