Thursday, October 9, 2008

What is a pharanegyal flap?

Just a little Anatomy class for today! For those of you who are curious here is a description and explanation of Grace's surgery.

A little history- She was in distress at birth from inhaling meconium in-utero which resulted in her being born with chemical pneumonia. She also had very low muscle tone which suggested there would be other issues. Then the adventure began! Long story but in summary, she was very mysterious for years and eventually at 5 was diagnosed with a rare genetic syndrome.

One of the things noticed just after birth was that although she would nurse or take a bottle, she wasn't able to get anything out of it. That is how we discovered she had a cleft in the muscles of her palate. So although her palate looked normal, the muscles underneath were not connected. At 6 months old, they were able to surgically connect muscles in her soft palate. Then with LOTS of therapy she was eventually able to use them with some degree of efficiency . Those muscles help with swallowing and speech. The creation of the pharyngeal flap has been suggested since she was 3 but because of her other issues and her small size, they kept delaying it. This year we begged for them to do something. We went with the saying, "if there is a will, there is a way". They agreed that the window of opportunity was closing for her to successfully correct the speech patterns she has created in an effort to compensate for the defect. So they began to think out of the box. Her anatomy did not allow her to make many of the sounds we use in communication. For example, prior to the flap if she were to blow a whistle nothing happened. If she pinched her nose closed though, she could blow it and make a sound. So in sounds that need pressure the air was escaping her nose. Which results in her sounding like she is talking while yawning. This flap changes the anatomy and gives her the ability to make those sounds. However, the muscles have to strength and adapt to it. It also involves a lot of motor planning but she now has the potential to speak clearer. We will continue to invest in LOTS of speech therapy- man, how I wish there was a return on investment there! The solution the team proposed, after our appointment of desperation, was to do the flap BUT only if they secured the airway with a trach. And that is how we got the flap and the trach.


A huge misconception, and frankly prejudice, is that if you can't speak clearly then you must be retarded. This was one of the main reasons we were so adamant about doing this for Grace. Although signing is an excellent alternative to verbal speech Grace has poor fine motor skills and so even that would have to be approximated. We have tried communication devices too but Grace truly has a desire to communicate with her words. For years she thought it was everyone else's hearing that made them unable to understand her! Once she realized it was her and not the listener she was already sold on verbal communication. We have been very intentional about telling her that although her words are difficult to understand she still has very good things to say and her thoughts and ideas are great and well worth explaining! Granted, it takes a lot of effort as a listener to understand Grace, but it is well worth it. She is very funny and intriguing. The goal of this surgery is that it will be easier for her and the listener and she will be able to communicate effectively with us and the average Joe.

So if you like the gory details this will explain how they did it...

They cut a piece of tissue from the back of her throat and and this is the flap. They then cut open her soft palate back by the uvula, separated it inserted the flap, then closed it back up. So it is sort of like a bridge across her airway, from the back of her throat to her palate. This is not normal anatomy it is a compensation for not having normal palate length, tissue and muscles in her palate. The flap covers a portion of her airway and thus the trach. Before the surgery and in normal anatomy the airway is open and now with the flap is taking the middle part of it. For instance instead of a circle it is now a circle with a thick line through it. Her breathing from her nose will come from the sides of the original airway and from her mouth rather than a wide open airway from her nose. This takes her brain learning how to adjust. While awake that is rather natural but in sleep with the body and mind relaxed the risk is that the brain doesn't adjust it's breathing and she stops breathing. The trach is an insurance for her, not her main airway but when asleep she uses it to breathe until her brain adjust to her new anatomy. Temporary but necessary. There you have it! Rather useless information for most but now you have a new word for Scrabble...pharyngeal.

16 comments:

Anonymous said...

Bridget,
Thank you for the explanation. This is fascinating. It sounds as though these doctors have done some very creative thinking and pioneering procedures. You are so lucky to have access to these skilled professionals who have the best science and most modern technology at their disposal. And I know the doctors are enjoying working with our dear Gracie, you and Darrell.
This record of your journey is so wonderful to read [even the days that don't go so smoothly!] :-)
Much Love to all of you-
Lynnette

Cahills said...

Hey Bridge - thanks for detailed info...I'm excited for the whole world to know this bright, hilarious little soul when she can communicate more effectively!:) Amber

Cassidy said...

Thanks for the anatomy/surgery lesson!

Anonymous said...

I'm sure you never thought you would know all that, but here you are teaching a fascinating lesson! Thank you! Don't children lead us on the most amazing journey? Thanks for being such a good mom and good example to the rest of us on standing up for your children. Love you guys,
Amy L.

Anonymous said...

THANKS SO MUCH AND WHAT A GREAT WAY TO BE SURE ALL HAVE A BETTER UNDERSTANDING OF THE PROCESSES! MARKETING DEGREE, I SAY YOU COULD BE A TEACHER, DOCTOR, OR EVEN A SPEAKER, BRIDGET, IN ADDITION TO ALL OF YOUR OTHER TALENTS. I KNOW YOU AND DARRELL ARE SUCH A WORLD OF KNOWLEDGE AND SUCH CAPABLE PARENTS. EVERY DAY I THINK OF YOU GUYS AND YOUR AMAZING STAMINA. I AM VERY PROUD TO SAY I BELONG WITH THIS FAMILY, AND YOU GET A HUGE CREDIT FOR THAT. ROOTS ARE STRONG AND YOU ARE DEFINATELY PLANTING THEM IN YOUR CHILDREN. LOVE TO GRACE AND HER AMAZING PROGRESS WITH ALL THE NEW TECHNOLOGY AND SHE WILL NO DOUBT BE TELLING EVERYONE THAT AND MORE. YOU GUYS ARE SO AWESOME. LOVE, NANA

Anonymous said...

You should write a book Bridg! Thanks for all the details.
Miss you guys! I love you Gracie!! I hope to see you soon.

Love, Aunt Sheri

Anonymous said...

Hi Grace,
I just finished reading your blog,
so glad you are home and doing so
well.
I just got back from the Cruise and
spending time with your MamMa.
So sorry the computers were not working on the ship. We thought about you every day and prayed for you, Judd, Carolyn, Mommy and Daddy.
Bridget the information helped me to understand what was going on. You are such a special Mom, and a
great Niece.
My Love To All.
Aunt Darlene

Anonymous said...

Bridget, I agree that you should write a book. You are such an interesting writer. Perhaps not a book on a medical topic, though....you might faint before finishing! You guys are still in our daily thoughts & prayers and we are so blessed by your family's faith, perseverance and positive attitude. We are so fortunate to be walking through life with you!
Love,
Denise
Denise

Anonymous said...

Grace, I hope you are having a good time with the nurse & teacher coming to your house! I bet you can teach them a few things, too, right?!? We hope you are getting used to your trach and that you are just feeling fabulous. We will look forward to seeing you some time soon!
Love,
Mr. Josh, Ms. Denise, Hannah & Grant

Anonymous said...

Wow! I am impressed with such a simple explanation for what I KNOW is a very complicated situation. You are ever in our prayers. God is so faithful in that one day you will be amazed at the "returns" on your diligence in pursuing better communication for Grace. He has something for that girl to say and there is no doubt she is going to want to say it! We send our love for your days and prayers for perserverance, endurance, stamina and abounding mercy in the midst of "fly-by-the-seat-of-your-pants" days. Love,
Chad & Alena

Cahills said...

Just checking on everyone - Grace I miss you! Bridget, it is an option - you WILL write a book? :) Sooo talented! Amber

Anonymous said...

Bridget,
I finally had time tonight to check out the blog and I am thrilled that I picked tonight! I loved getting to know what Grace's situation is all about and what she is going to be soon! I love mostly that you are totally His and that I can see God working in and through Grace in mighty ways because you are so obedient and full of faith. You are all truly amazing!
Prayers continue with love,
Carol Watson

Anonymous said...

Bridge-
It is not useless information. It helps me connect with Grace and the rest of the family being to have a better understanding of what is going on. And I appreciate you taking the time to explain it all.

I admire your strength, love and miss you very much.

Becky

Ashley said...

That was just a perfect description of what Grace has been through and this last procedure; I am a "need detail" kind of gal and it totally helped me with the great scope of things! We have continued our fervent prayers for wonderful healing and for REST for each of you! I'm bringing a meal for you guys tomorrow so work up your appetite and I look forward to seeing all of you; should I get orders to bring over a Starbucks I.V. bag?!! :)

Anonymous said...

Hi Grace--

Grant was wanting me to see about scheduling a bike-riding date with you. It sounds like you are a pretty busy young lady these days, so can you check your calendar and let us know when we could possibly come over and ride bikes? Maybe next week sometime? If it is OK, Ben would like to come, too.

Ms. Heather (on behalf of Grant and Ben)

Anonymous said...

Hi Grace:

My name is Mary and I use to work with you Grandpa Dean. I have followed your big event everyday on your blog site. Haven't seen anything lately so I just want to say that I hope you are doing great. Your really an amazing young lady. Your family can be very proud of you. Good Luck with everything.