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Tammy,
Thank you so much for your kind words- It really was my joy to design for you and Parker.
Emma has a G-tube, and it was equally hard for me. I am always here for you to chat with if you have any questions or concerns about it- Emma has had a G-tube most of her life.
You arent alone
Heather
I will be praying and adding Parker to my prayer list. God Bless you all.
I will praying for Parker and also for you.
Keeping your sweet little guy in my thoughts and prayers…and will try and figure out how to add that adorable side bar button.
Peace, TM
You know Parker is always in my prayers! I am having trouble with my own blog today, but I will try to get the button added when I’m able to!
You know something, I don’t believe Kayla weighed much more that Parker at his age! She was not 20 lbs by her 2nd birthday. I remember it was May when we were leaving for a trip to MD and I turned her car seat around because he was 19 lbs and I thought that was close enough to 20 lbs LOL We had 1.5 hr trip to the airport and I wanted to keep her occupied by playing the ST DVDs – which meant she had to sit forward. In May she was 22 months. I know Parker has a lot of other issues, but just wanted to let you know Kayla was only a couple lbs more than him at that age. She was (and still is) small – she’s only about 25-26 lbs now at 38 months.
Hugs to you on the decision about the g-tube though.
Oh Tammy. I hope he doesn’t have to have it. But if he does, be encouraged by Heather. I didn’t realize Emma had a g-tube. I imagine it’s like everything else. It’ll take a little while to get used to the new routine. But if it will help him, then of course it’s worth it.
Thought I’d let you know I did put his adorable little button in my sidebar and linked so people can click on it and come directly to his site. Heather did a great job. This is an adorable site.
just happened on to you blog, and wanted to let you know I too have a child who in 12 short years has had 15 surgies due to being born with spina bifida. Jesse and I will pray for God to send down His Healing Rain on your beautiful Parker……..sincerly sonja brooks
I prayed for both of you today. I wish I understood adding buttons/links and things, but I don’t know how. If someone wants to show/tell me how I would love to put Parker and Emma’s buttons on our site.
Y’all are in my thoughts daily.
saying lots of prayers for sweet little parker!! give him a great big hug for us, ok?
I found Parker’s website via Barb, and I will be honored to place his button in my sidebar and link back here to his site. Bless his little heart, I pray God will bless him and your family.
Diane
Parker is always in my prayers, but I will add a special prayer about the G-tube. I’m hoping he won’t need it but, if he does I hope the procedure to add it goes well.
I think I might have been here before. I get lost in all the blogs. I have a hard time keeping track of peeps. I apologize.
My son Ethan is three. We have been fighting a G Tube for a LONG TIME. Well, since the NICU days. Ethan was born with a systemic infection that lead him to have all kinds of issues. He is Deafblind and has Moderate Cerebral Palsy.
I have just never had a good feelign about the G Tube. Not ever. I just feel icky about it. We have tons of friends that have them, and love them, and are grateful for them, but like Parker, Ethan has other issues (A really really big liver) that would make a G tube, something a little more intricate, than is typical.
I am sure you have heard all the suggestions in the world, but something that worked for us, in weight gain, was olive oil. I add it to his formula regimine.
Ethan came home from the NICU with an NG tube, on fourty percent po feeds. This was in April, we finally got him to take everythign from a bottle in October ( I really thought it would just take a week or two.. um ya) But weight gain was a hard reach for us, but oil has worked. HE still isn’t eating by a spoon. Not one tiny little bit, on a regular basis. WE keep trying every day..But currently with fortified formula he is slowly gaining weight.
They keep talking to use about G Tubes, but.. I keep ignoring them.
I’m not sure, we are doing the right thing. But for the moment, it is working for us.
Our prayers are with ya~!
Oh Tammy – sorry about the whole G-tube thing. We are hoping and praying that Parker doesn’t need it, or if he does that it will only be for a while, maybe until he has his repair surgery?
Your sweet boy is in our thoughts and prayers!!!
Hugs from Brady and I….
Parker is already on my compter-side prayer list, but will add these specific concerns. I’m not only praying for HIM, but for ALL OF YOU.
LOVE your site design. The first thing that caught my eye was your new Pray for Parker button. As cluttered as my sidebar is already, I will definitely add it there. Maybe not today, but it will be there.
I found Parker’s website through Barb, and I will be adding his link to my sidebar. My prayers are with you!