Monday, September 27, 2010

Tomorrow Morning

Maya's surgery has been scheduled for tomorrow morning at 7:30. Please keep her in your prayers! I will update as soon as I can...

Thank you to all of our family and friends for the continued support as we go through this journey... we could not do it without your love!

Saturday, September 25, 2010

Post-poned

I just got a call from the surgeon's office... Dr. Kupferschmid is stuck in Asia and will not be able to do Maya's surgery on Monday. He does 4 or 5 mission trips a year and we knew that he would be out of the country saving the lives of those children who are in desperate need. He also takes equipment and trains other surgeons while he is there. Unfortunately, his flight home has been delayed and so will Maya's surgery.

So now, we will wait until Monday to find out the new schedule. It is possible that it may just be moved to Thursday, though those plans are tentative. I truly feel like everything happens for a reason, and this is part of God's plan. While the waiting and not knowing can be tortuous, I know that He is in ultimate control.

Thank you so much for your continued support ... it means so much to have so many people praying for us!


I will post the new schedule as soon as we know it...

In Him,
Brandy

"Trust in the LORD with all your heart and lean not on your own understanding; in all your ways acknowledge Him, and He will make your paths straight."
Proverbs 3:5-6

Monday, September 20, 2010

Getting Technical

For those of you who would like specifics, see Kevin's version: As you can tell he his much more technical than I am :) Hope this helps clear up any questions...


Short version: We met with Dr. Kuperschmid yesterday. Maya will have surgery Monday September 27th at 8:30 am at Methodist Hospital in San Antonio to repair her mitral valve and most likely she will be fine with that until she is 20 or 25 years old when they will have to replace a ring around the valve as she outgrows it. Worst case scenario is a mechanical valve that would make her life different from ours.

Extended:

They will give her a liquid Versed to calm her before either Brandy or I take her to the OR and they will give her gas so they can insert the IVs, transesophageal echocardiogram tube, ventilator tube, stomach tube, catheter, and arterial lines for the bypass.

He said the riskiest part of the surgery is actually the sternotomy—entering the chest with the heart pressed against the breastbone. If the saw hits the heart, he said it “is a bloody mess for a while.” This has happened twice in his 20 years or surgery, so chances are that this happens are almost 0.

After that, he said they would put her on heart bypass and inject the heart to stop it. Then, they will enter sort of where they did before on the upper left (facing her) side of the heart wall, then cut through the atrial wall, and work on the valve from that side. I was expecting them to enter on the right side as this is where the valve is. When I asked him how big a hole this is to work through, he held his fingers about an inch and a half apart. So, on the attached pic, they will enter on the upper left atrium, go through the wall, and work downward on the right valve: that white thing with all the strings hanging down from it on the right side.

The valve itself sits in a muscle ring called the annulus—where the white valve connects at the top. Maya’s is not the shape it should be so they will stitch in a ring called a Carpentier ring to fix that. The flaps in the valve are tethered down to the lower part of the ventricle walls by things that look like fine strings and the closest one on the pic has strings that are too short on Maya’s, leaving it unable to close completely enough. He said he would just cut the ones that are restricting it and that should allow that side to close better. The other valve flap (the back one in the pic that you can’t really see) has an apparent cleft in it which will either be stitched in a manner so that it closes better or resected and rebuilt out of surrounding redundant tissue.

They will then close the atrium and heart wall, allow the heart to restart and look to see how much regurge (leakage back up into the atrium when the ventricle contracts) is showing on the echocardiogram. If it is good enough, they will close her up and get her off the ventilator as soon as she can breathe on her own. He said that if things go well the surgery will take about four hours. It doesn’t look good, they will re-open the heart and try again.

He said he was 75% sure they could repair this as described above, but even with the pictures they took most recently he was unsure if he knew exactly what he would find once inside. If the valve cannot be repaired to his satisfaction, they will insert a mechanical valve. If this happens, Maya’s life will be significantly altered because she will have to take blood thinners for the rest of her life. This means anything that makes a bleed (internal or external) is far more dangerous to her than a normal person and she would be unable to have children of her own because of the effects those drugs (Coumadin/Warfarin) have on young girls. The valve will also have to be replaced at times.

If everything goes to plan, the insertion of the ring on the annulus remains a small problem and will begin to be too small for her at some point. He said probably around age 20 or 25 she would have to have this surgery again. By that time, though, it should be relatively easily done because of her size and the technological advances.

Personally, it helps me to go through all of this to sort of callous me a little and dampen my fears by pretending that understanding is controlling. Brandy is taking it pretty hard, and the prospect of the mechanical valve really has her worried.

Your thoughts and prayers are appreciated.


Friday, September 17, 2010

Prayers for Maya...


The date for Maya's surgery has been set for Monday, September 27th. Yesterday, Kevin and I met with the surgeon that will be fixing Maya's heart. He is an amazing doctor and it is was good to finally get some answers to the what if's. Her surgery will be open-heart and she will be put on bypass (heart/lung machine). Once her heart is still, he will go in and reconstruct some parts of her mitral valve that are not lining up properly and causing it to leak. He will then place a ring around the valve to tighten it up and help it be more stable. She will then be taken off bypass, and they will test her valve to see how it performs. He will continue to make adjustments until he feels satisfied that the problem is fixed.

If that does not work, he will put a mechanical valve in as a last resort. Mechanical valves come with many complications, so we hope that will not be necessary. Most likely this will not be a permanent fix. Her valve is not big enough for an adult ring, so a teenage-sized ring will be used. He said it is possible that this work for a long time, but we may be looking at replacing the ring in ten years. He felt 75% certain that he will be able to fix it without having to replace it and that is what we will be praying for. The most dangerous part of the surgery will be re-entering her chest, since her sternum will have much scar tissue from the previous surgery. I ask that if you see us out, please don't discuss the surgery in front of Maya... while she knows what is going on, others' concern can raise her anxiety. If you have any specific questions, feel free to call or email me.

We will be spending two days in Pediatric Intensive Care and probably two or three more days in a step-down unit. Should he have to put a new valve in, we will be there a week or more. The first 48 hours will be the hardest and she should start feeling much better after that. I ask that if you see us out, please don't discuss the surgery in front of Maya... while she knows what is going on, others' concern can raise her anxiety. If you have any specific questions, feel free to call or email.

Thank you for all your prayers and support. You have no idea how much it means. The day of surgery and throughout the hospital stay I will post updates on my blog. I want to make sure that people are not left out and that seems like the best way to keep everyone updated without having to keep track of a million email addresses. Also, so many of you have offered to make meals that I could not possibly keep it all straight. Our friend Stuart has set up a care calendar for putting it all together. Please do not feel obligated, if everyone did we could feed a small country! But it is there for those of you who want and are able to help.

Blog: http://brandycwebb.blogspot.com/
Care Calendar: http://carecalendar.org/logon/50973
Calendar ID: 50973
Security Code: 8893

Please feel free to forward this to anyone who knows and loves sweet Maya. I could not possibly gather all the email addresses and it is likely that I have missed someone. Please keep her in your prayers and thank you for all the love! If I have not answered your email or called you back, I promise I will. Right now the scope of it all is a little overwhelming so I am just taking it day by day. I know that God has a plan and He loves her and will take care of her... and I will trust in Him.

In His Grace,
Brandy

Fair Day!


Check out these cute outfits for the Comal County Fair!


Aren't they Simply Adorable?


I think so!


Come see us in Gruene this weekend, Email me or go to Simply-Adorable.com to order.


Have a great day!

Friday, September 10, 2010

First Day of Kids Kare

Yesterday was Maya's first day of Kids Kare. She was really excited! The first day was actually Tuesday, but she was tired from our Marfa Trip (will post pics later) and it was POURING so we decided to stay home. So... she got all dressed up and headed off with Daddy for the first day...


and I think she had fun-- until she started feeling bad. Ms. Melissa called around 11:30 and said she was in the office with a tummy/headache. I think that Kevin and I both thought she was more homesick than realsick... until she threw up in the car on the way home! Poor baby. I guess the graham cracker she ate for snack just didn't sit well.


That's okay... we'll try again next Tuesday!

Friday, September 3, 2010

Prayers for Maya

Please keep our little Maya in your prayers... she will be having another open-heart surgery to fix her mitral valve. I will be updating this blog as we know more information, but surgery is likely to happen in the next 30 days. We sincerely appreciate all of your kind words and well-wishes. Thank you for your love and support!

The Webb Family
Kevin, Brandy, Parker, Rain & Maya