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Joey Samuel Lawrence

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 Born Jan. 17, 2007 

   Saint Joe’s Hospital in Tacoma, Washington (WA) - Trisomy Mosaic

6-14-07
Hi, my wife and I had our son Joey Samuel Lawrence Jan 17 –07, this was a great moment in our life as we have 2 other children Jardana age 11 and Jackson age 2 and a half we were surprised and thrilled when we found out that we were going to have one more as my wife was 40 and I'm 35 we didn't think it was going to happen.

Agara my wife said she was going to get fixed so we wouldn't have another child because of her age but 2 weeks before the appointment we found out we were pregnant with our son Joey I was wanting a girl and was going to name her Jillian but as the pregnancy progressed we found out that we were having a boy so Agara got to name him also as the pregnancy progressed she was told that our son had the chance of being a downs baby, this was not a big issue as they told us that Jack was going to be a downs baby this test she was given had to do with her age and had a low number of being right and as we discussed it together we didn't care we felt that God gave us this last chance to have Joey that we would endeavor it and all that was to lei in the future as only God would of known what the future would have in store for us and Joey.
I guess the news came when she was 7 months almost 8 months along that Joey really had some kind of problem that was facing him and my wife and I as they told us that Joey just had a cleft lip we thought well that's not to bad a few surgery's and he would be as good as new Agara and I never had any thoughts about it we just felt lucky that we were having him and God wouldn't give us a baby that had lots of problems.

By this time our doctor was asking us to come in for check ups 3-4 times a week this is when we started to get nervous Agara gained more water then a normal pregnant woman would of gained which made things even more complicated for us and the doctors.

For us Agara couldn't get out of bed or get up of the floor or even get out of a chair it was also hard for her to drive as she looked like a water buffalo ready to burst.

For the doctors they couldn't see if anything else could be wrong with Joey because there was just too much water in the bag for them to get good pictures or sonograms and as this started to worry the doctors Agara started to have complications such as high blood pressure and vary bad swelling in the ankles and her feet it seemed that she started to spend a lot of time in the hospital this also started to stress her and the baby out and we almost lost both mother and child.
December came along and Agara was 7 month along with Joey when I wrecked my truck and lost a cargo load up on the mountain I wound up unemployed and un able to work this stressed Agara out so much that it almost killed her and Joey because we had no money in savings and didn't know how we would make it as I have no other skills but truck driving I had no clue what we would do.

while she was in the hospital, that time they convinced her to do the amniocentesis which is when we found out that Joey was a trisomy13 baby. Agara and I had no clue what that was to mean until they started to bring in experts and we found this site that is when my heart fell this is when things started to go ways we never anticipated.

As this new started to trickle down though our friends and family it seemed the weight of the world was crashing down around us Agara and I had no idea of what we would be in stored for us and our family because things just kept looking worse and worse, they told us around the 9th of January that they was going to induce labor and that Agara had to stay in the hospital until then.

I got scared and started to ask every one I knew that was religious to pray for us I asked our church and members of other churches to keep us in their prayers I can't remember much between the 9th and the 17th because it seemed like all I did was cry and being a guy I cried a lot even at the mere mentions of baby's or of faith God Joey or Agara these all seemed to trigger my crying, to the point that I started to blame God and myself for this problem we were facing.

I just couldn't understand why God would give a baby that had so manyi problems to parents like us parents who didn't do drugs, parents who never sold drugs or abused our children in any way or had ever or even thought of committing a sexual act with a child for in my mind those are the bastards that should have children with problems like ours and I started to feel alone in this time of need this was the time that my wife the woman I love and cherished needed the support that I didn't know if I had it or not.

I stopped going to church and felt that God had abandoned me or us at this time I wasn't sure what it was.  Then the day came that Joey was coming into the world weather we were ready or not they induced labor and it wasn't long after things started to turn. Half our congregation from church was there as my sister and a friend of the family, that's when I found out just how lucky we were.

Joey started to come out when the cord got pinched and our doctor gave us the option of having him alive or dead because if she kept going natural birth he would die and the doctor wasn't sure that if he gave Agara a c-section if Joey would live any ways he told us that typically these baby's don't live long after birth and it would be hard to tell, my wife and I locked eye's I started crying and begged her to have the c-section telling her that I didn't care if I only got 5 minutes with Joey then Id be ok with it As Agara had felt the same she was wished off to an emergency word for the c-section.
I started to pray to God asking him for an exchange an exchange that in my mind was fair I asked God to let our son Joey to live and in Exchange if I could spend five more minutes holding all my children to tell them all how much I loved them that God could have my life instead of taking Joey's our pasture said it didn't work like that as I sat there in tears not knowing if I would even get to hold Joey or not.

My pastor and the rest of our church started to pray as I sat there deep in my own thought wondering the future and what was to be in stored and feeling angry that this was happening to us loving parents who would lay down their life for their children when there was those other people that didn't deserve healthy children and then it came to me as I see it divine intervention slapping me in the face.

Our pastore Bob had come over to where I was crying and feeling sorry for myself and said Stan God only give special children to parent who would love and care for them parents that no matter the time or cost would love and adore and do for them that parents like the drug user or child abuser cold not love or take as of good care as me and Agara could with Joey that God only gives special baby's to special parents and that we were to be blessed with the arrival of Joey.

I can't say that I always agree with Bob but I know that God only gives us as much as we can handle or so they say I some times question that too as I feel my knee's are buckling and don't know how much more I can take.

I still haven't gone back to work yet as I was fired from the last trucking company I worked for and I'm still under an investigation for the truck wreck by the D.O.T. and this is the May but I hope to be working soon because we have gone though all the money we had received from a sale of a house that was willed to me and unfortunately the house we now live in and own is falling in around it's self we have only one burner to cook on and our oven went out because we used it to heat the house and come this winter I just don't think we will make it too long with the mobile home we live in no heat no even and it's starting to fall in on it's self but I can say this at least we own it out right and we don't have to pay for anything but taxes on it.

We tried to go out and buy another mobile home a new one or have a house built for us but our credit is so bad from outstanding hospital bills and other things that we can't get a loan besides that I had to go out and buy my wife a new van so she could get back and forth from the doctors appointments that she has with Joey that it now show's we're paying for a 25,000 dollar van on our credit that makes things tuff for us but I'm sure we will make it I hope to be back to driving truck soon.

Joey goes to the Doctors 2-3 times a week he has a new feeding tube in his stomach and is doing fine he has gained 10 pounds and were waiting to see if their going to do the lip surgery and they say when he is 2-4 they'll do the cleft pallet surgery our hopes and prayers are with him that he see's life that long and longer as they keep reminding us that these baby's are special and some time don't make it that long but we have the faith of God and a whole lot of prayers going for us they say that Joey is deaf but has his sight and that maybe when he is older they can do something for his hearing as he has water or liquid in one of his ears they might be able to save that when he's a little older.

We'll I hope this is what this is for that we were to tell our story and that they would put it in a document for others to read and that I didn't just waste a lot of time typing because this is our story and I felt I needed to tell it to let people know that their is hope and that God does care and takes care of his own thank you and God bless

The Lawrence Family
Stnuctew3@aol.com

 

Submitted 6-14-07

 

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Text and graphics © LivingWithTrisomy13.org 2005-2007 All information found on this site was submitted to us directly by the families and used on this site with their permission.
Cover photo of Pamela Sullivan & her precious daughter Maria, copyright Pamela Sullivan 2004, used with permission.
If We Hold On Together  Song Copyright 2002 by Patricia Welch, Ltd. All rights reserved.   Used with permission.
 
*Disclaimer
All material on this site reflects our personal journey with raising a Trisomy 13 child. It is not meant to replace any medical advise of a professional familiar with your specific condition. The personal journeys of any parents on this site are only their opinions and their own journey with having a Trisomy 13 child. You should consult with your own physician or other medical professional regarding the opinions or recommendations expressed within these pages as to your own child's symptoms and medical condition.
 

Looking for ALL families who’ve had a trisomy child of any number. Whether you terminated, miscarriage, had a stillbirth, live birth - living or deceased. Including adoptive and Foster parents. Please fill out the TRIS survey  to help update the medical literature and to improve the quality and availability of medical care. Tracking Rare Incidence Syndromes (TRIS)  Click here to add your information

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