Showing posts with label Liam Lyon. Show all posts
Showing posts with label Liam Lyon. Show all posts

Wednesday, June 13, 2012

I Can't Sleep...My Mind Is Racing!

As I start this post I look at the clock on my computer to see that it is 3:45am.  I have seen that number several times before since I have started this journey, but never has it been for this reason.  My body wants to rest, but my mind is not allowing me to because I have too many things that are running around in there.  All I can think about is Liam, Kona, The Movie, and the Future.  I am not sure how this post will finish, and it may be only for myself, so please keep that in mind before taking the time to read it.  I can also tell you that I have permission to speak about the information below from Liam's family.

For nearly a week now, I have been working with Liam Lyons family through Shawn's Anomaly.  If you have not had the chance to follow the posts on www.shawnsanomaly.org on the right side of the page, Liam Lyon was born nearly 16 months ago with 1/2 a heart.  He had a heart transplant at 6 months old that should have saved his life, but he has had complications with it every since.  Liam's family has been trying so hard for months to get Liam in to Texas Children's Hospital so he could get the care of some of the best doctors in the world, but they have underwent major hurdles to get him transferred.  Most of the reason that the transfer has not happened is because they have not been able to find an accepting doctor at TCH.  Of course, that got me involved because I know how great TCH is.  I mean, they saved my son's life!  I just did not understand why they were not allowing Liam to come to get treatment.   

Of course, you can't fault anyone at TCH for not wanting to accept Liam.  After all, Liam is really getting very good care at The Children's Hospital at St. Francis in Tulsa, OK by Dr. Barton.  I don't envy his job at all.  He has done a lot since Liam was transferred into his care from Arkansas Children's Hospital pretty much as a hospice patient since the surgeries and Liam's current position does not make him a candidate for another heart transplant.  Unfortunately nothing has seemed to work.  You would have thought he would have given up a long time ago, but Dr. Barton keeps pressing on for Liam and trying everything possible to help.  He has tried already to get Liam into TCH, but unfortunately the decision was made not to accept transfer because they felt there was nothing else that TCH could do better.  I cannot fault their decision at all.  

Recently, they found that there is now a hole in Liam's trachea from the tubes they put down his throat to help him breath.  This of course changes everything because now the ENT doctors at Tulsa do not feel comfortable performing the very risky surgery on Liam to fix the hole.  Again, Dr. Barton has requested that Texas Children's Hospital to accept Liam now hoping that a doctor at TCH will be more willing to perform this extremely risky surgery.  After all, how many doctors do you know want to perform a surgery on a child just to watch that same child not make it out of surgery.  The chances are very low that they will find a doctor who will be willing to accept a transfer at TCH, but at least TCH is considering it.  

The transfer to TCH would really be great for not only Liam, but the family.  I know that they have been through a lot in the past 16 months.   Liam's Aunt already lives here in the Houston area and has really been leading the charge, but you can tell in her eyes that she is tired.  They are all exhausted, but they don't give up on Liam.  You can also see in Liam's eyes that he is a fighter.  He does not want to give up either, so because he doesn't, the family doesn't either.  They are praying daily for a miracle, and now so am I.

As parents you may sympathize with their situation, but you may never understand how hard it is and how alone you sometimes feel during the process.  I pray daily that you don't.  My wife and I do, and just sharing our story and our experiences with Liam's family seems to help.  We can't do much financially right now through Shawn's Anomaly because we are just getting started and the donations just don't seem to match up with what I would love to offer them, but we are trying our best to be there for this family and others just like them.  After all, that is what Shawn's Anomaly is really all about.  It is not about finding a cure for Shawn's conditions or about saving kids lives.  That is what the hospitals are for.  Shawn's Anomaly is about providing education, hope, and help to the families of these children. We want to let them know they are not alone and there are other people who have, "Been There, Done That!"  That statement, believe it or not, goes a long way. 

I often feel that I don't explain that mission better, and for that I hope that you will truly accept my apology.

I realize now after seeing what I have written, it would be crazy for me to continue and tell you the other reasons why I can't sleep in this post, so with that being said:

To Be Continued...

In the meantime, I ask you to pray for this family, pray for the decision that TCH is currently underway making, pray for Liam, and lastly pray that I get some sleep.  I am going to be useless to this family and other 1-in-30 families that are dealing this birth anomalies if I can't get any sleep. 

Tuesday, June 5, 2012

Calling All Shawn's Anomaly Supporters

Do you want to see the Shawn's Anomaly Mission (Education, Hope, & Help) in full action?  Well this is where we as supporters can come together to help little William Elija Lyon, affectionately dubbed Liam.  This family is desperately trying to get their baby to a doctor at TCH that can help with Liam's congenital heart anomaly.  We have contacted the family to see what we (Shawn's Anomaly) can do to help, but we need all hands on deck to brainstorm on what we can do.  Please see the latest correspondence:


5/20/12 Last night Whitney called me to let me know that they were doing "parent care" - which is like the step down unit at ACH - the parents room in with the child and do all the care - just as if they are home. This is a BIG step towards going home. So for those that read this part of the page - we have a couple of options for transfer. Our first choice was to get an accepting doctor at Texas Children's and transfer him for a complex discharge. Basically get him here and evaluated and then discharge him to home (my house) after they were certain we were prepared and they had a good baseline on him. Not happening. Our next choice was to transfer to a transitional hospital in Houston - it is kind of a skilled nursing facility for chronically or serioulsy ill children - and it would only be long enough for them to evaluate and make sure we were prepared for home care. The hitch is they are concerned about Liam and want to be able to reach out to TCH if there is a problem - which is totally understandable - he can be a handful! This option is pending - and we would really love to see this happen. And if he transfers hospital to hospital, he will get a medical transport. The last option is he gets discharged to "home" from St Francis. They have said he can't go to his home in Cameron - it is too far from a large children's hospital that is equipped to deal with transplant kids. So "home" would be to somewhere safe in Tulsa. But Liam needs specialists in cardiology, pulmonology and trach care, nephrology, enterology and developmental. All systems are pretty optimal right now so we really want to get him to Texas as soon as possible! If he is discharged to "home" we will have to provide the transportation - that means an approximately 11 hour drive or a private flight in a small plane with an unpressurized cabin. We have volunteers to fly (3 pilots) and a plane, and even a pediatrician who has volunteered to fly with him. So we wait to see if he gets ready to discharge before he gets transferred. Either way, he is really, really doing good. And we got a crib off Craigslist - once the folks heard his story they wouldn't take any money for it. Whitney and Cheyanne fly to Houston tomorrow. And we are going to meet with some people and go see the transitional hospital. Keep us in your prayers - and keep Liam in your hearts - we are still following the path our hearts and prayers are leading us down. 33000 strong - what a journey this little boy is taking us on. Just keep swimming, just keep swimming.



As I have seen what the masses of support can do in the past, let come together for this little miracle and help his family.  If you can offer any type of assistance, please contact us immediately at shawnsanomaly@gmail.com