Please Watch! One Congenital Heart Defects Story.
Uploader Comments (pennyzeigler)
Top Comments
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Thank you For this Video My heart goes out to you ! God Bless you! We are trying to Spread Awareness I hope that many people get to see this !
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I am sorry I made that interpretation from the video from what was said about his last wish. Thank you for correcting me on that. I hope that you, Michael and your daughter have many, many more years of happiness together. I am so relieved to know that he is still with you and your daughter. My prayers are with you always. I continue to spread awareness about CHD in our Angel Landon's memory, please continue to share your story as well.
Love and Prayers to you and your family always
Video Responses
All Comments (26)
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Wonderful that the little boy in this video with a CHD grew up to be a sweet man.
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i had the mustard procedure done when i was 6 weeks old in 1972.my parents were told i would be lucky to live through the surgery let alone to age 5 i'am now 39 yrs old have 2 great sons and a new granddaughter.i had no real problems growing up until after the kids were born.i'am now on my 3rd pacemaker and one day will need a heart transplant but everyday i wake up i thank the good lord for giving me more then my fair share of life.if u have faith and are strong u can overcome anything.
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I also Have Congenital heart defect. T_T
I had immidiate surgery right WHEN was BORN.
I am currently doing fine now though. god bless the people with this disease.
You are not alone.
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@pennyzeigler i've had that same operation i am 22 now and have been doing ok. besides a few miner health issues.. I hope all is well with your husband.
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Hello
I had mustard surgery in 1967 in LA CA
I was born in 1964 july 31.
the first pic in your video really hit home with the black and white photo.
I live in carson city ,NV now and am 46 years old and on pacemaker # 5
If you like to e mail me feel free at megodude@charter.net
If you still live in No Cal I sure would like to talk with an meet you
Hang in there
Kurt lepire
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I also have TGV and have had the Mustard procedure done to correct the TGV. I was 13 months old when I had the surgery done. I was also the first survior at Henry Fords Hospital of Detroit,MI and 125th in the world to have it done-back when they still counted. when I was 32 ZI was told within 10 years i was lookimg at a heart transplant, am now 42 and still kickn' :). I have had a pacemaker put in in 89, replaced in 95 & 2006. I am in the beginning stages of CHF. and also have atrial flutter.
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aww im sooo srry =(
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im 20 years old i have the same thing and the mustard procedure i never got them switched .. i have a pacemaker now for 3 mnths
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Im very sorry to hear about that. My son was born with D-TGA in June of 2009 He had the arterial switch done. Which is different from the Mustard. I would love it if you could keep me informed on how your husband is doing.
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Dont get me wronge but there no really support out there for familys that are possible face death every day. I just happy what time I have with my husband. Sorry to be so low today on my replay. I had a hard day!
It has been nine months since the last comment on this thread. How is your husband doing? What are his complications that are causing him to require a new heart? I have the mustard procedure myself. I was born in 1980 and I have been healthy my whole life (I've been told I am very lucky, and that most don't do as well). But now at age 29, I am beginning to develop arrhythmias (for the first time ever). It's scary. My cardiologist is referring me to other specialists now. Please message me
grybold 2 years ago
My husband is D-TGA. Thanks so much for commenting it really nice to talk to someone that has the mustard procedure done also.
pennyzeigler 2 years ago