Atrial Septal Defect (ASD) - Online Support Group

Hi everyone, we took Alyssa to the cardiologist on Wednesday hoping for the best case scenario.  Unfortunately, this is not what we got.  They did another echo on her and found another hole.  Because she has 2 holes and one is fairly close to a valve, they do not consider her a good candidate for catheterization.  We are pretty devastated but trying to act as normal as possible in front of her.  She will most likely have her surgery within 3 months. :(

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Comment by Julie DiMatteo on August 21, 2011 at 5:33pm
Thinking of and praying for Alyssa, you, and the rest of your family.  I know these are scary times for all of you.  I had my ASD closed via open heart surgery almost 15 years ago (age 18) - diagnosed in August and repaired in December, 4 months later.  I remember it was scarier for my parents than it was for me.  While open-heart surgery is scary in and of itself, the procedure is one of the most straight-forward of all open-heart surgeries.  In the end, it will all be worth it - Alyssa will live a healthier, stronger life with her repaired heart.  And, the best gift I was given besides my healthy, repaired heart, was a perspective to live by the rest of my life by.  If I have the courage and strength for open-heart surgery, I have the courage and strength to do anything.  Sending hugs your way!
Comment by bernardshuford on August 21, 2011 at 10:43am
Hope and pray everything goes well.  Get it fixed, regardless.  I waited far too long to get mine done, and it caught up with me badly.
Comment by Syl on August 20, 2011 at 6:51pm
I'm so sorry to hear this.  But stay positive! These doctors are wonderful and I am sure your angel will come out of this wonderfully.  She is in my prayers.
Comment by Syd01 on August 20, 2011 at 8:02am
Hi Alyssasmom
I wante to quickly drop you a note, as I had a slightly similar situation. While I only have 1 hole it was next to the valve as well. My cardiologist mistakenly told me he thought I would have to have surgery. It was once o started visiting the right surgeons that I was told my repair was an option with the Helex device - and even then only the 2nd surgeon I visited told me this option and had the specialist in helix (dr Kar)look at my case. I'm certainly not a doctor and don't know the implications of 2 holes vs 1, but just suggesting you consult a few drs. who are experts in the actual procedures. It wasn't until 4 months after I started seeing doctors (and 3 weeks before my procedure) I was finally told I didn't have to have surgery.

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