The DDA Trouble Free Zone Part 5

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tmfranlk said:
Okay, I posted on the dining board, but thought you all might be able to help more quickly. I currently have an ADR for dinner at Boma in October. I have been wanting to try it, but wonder if it is asking too much of Terra. She generally does really well in sit down restaurants and will eat almost anything. However, not having been to Boma or AKL I don't know if it is a little too dark/quiet/adventurous/long/whatever for her. Should I wait until she's a little older or go for it now?

When my granddaughter was 4, it was her favorite restaurant at WDW. I kid you not. And she is the pickiest eater in the world. She loved the little kids buffet, but ate so much stuff from the regular buffet. Plus the desserts. YUM!!! :goodvibes :goodvibes :goodvibes

We did dinner, btw... :cloud9:
 
KristineN said:
I have been fooling around with an xmas design for our trip...what do you think?
snowlake2.jpg

Very cute -- I really like it!
 
I'm off to bed. I've got another very busy day tomorrow so I probably won't be around until late again.

Deb
 
duckyfordonald said:
Thank you so much for the warm welcome! :goodvibes I have to apologize that I have not read through the 1,000+ pages :blush:, so I don't know the "history" that you all share. But I do look forward to posting more frequently and getting to know each of you better. You seem like such a caring, generous (and I can't forget TALENTED) bunch!!! ::yes::
Blessings, Shana

Oh Shana what do you mean you aren't going to read 1000+ pages?:confused3

:lmao: :lmao: :lmao:


:welcome:
 

tmfranlk said:
Okay, I posted on the dining board, but thought you all might be able to help more quickly. I currently have an ADR for dinner at Boma in October. I have been wanting to try it, but wonder if it is asking too much of Terra. She generally does really well in sit down restaurants and will eat almost anything. However, not having been to Boma or AKL I don't know if it is a little too dark/quiet/adventurous/long/whatever for her. Should I wait until she's a little older or go for it now?

Tia - Boma is one of my and DH's very favorite restaurants. While there are plenty of adventurous things on the buffet, many of the items are readily discernible, plus they still have a children's buffet with chicken fingers, mac & cheese, etc. And the desserts are TOO DIE FOR! We ended up not making it to Boma for any meal on our last trip, and I really missed it.

Boma is usually bustling with lots of families - I definitely would not describe it as quiet. I say go, and enjoy! :thumbsup2
 
triplefigs said:
DDA, I could use some serious prayers for Rees (and me) please. Here's some background so you'll understand the seriousness of this issue.

When Rees was born, he was our healthiest until day 2 when he crashed. He was so sick, and the doctor's didn't know if he would make it or not. They could not get him off the ventilator, and it was extremely touch and go. He had horrible time feeding, and was diagnosed with severe reflux (GERD). He literally spent weeks at a time in the hospital, with one stay 45 days just before his first b'day. He vomited up to 40 times per day, was in agony, on all types meds, had so many nasty procedures done it breaks my heart, was on feeding tubes... oh, it was just horrible. We would call the GI doctors at 2am with him screaming in agony, refusing to eat at all, arching his back. We'd end up in the ER, get admitted again, go to the PICU. It was a vicious cycle and some very dark days. Finally at age 17 months he had a major surgery called a Nissen Fundoplication. A Fundo is a drastic and last resort surgery for these kids. They literally go in and wrap the child's stomach around their esophagus to physically prevent any acid for regurgitating out of the stomach. It has lots of side effects, and the kids are unable burp or vomit afterwards, so you must be very careful with stomach flu, food poisoning, swallowing pennies (ok, that is funny). It was MAJOR surgery. He was in the hospital for 10 days, has an incision from his breast bone past his belly button (looks like open heart surgery). Up to that surgery Rees was Failure to Thrive and only weighed 15 pounds. The reflux and long hospital stays and pain are a major reason he is developmentally delayed.

Well, 3 weeks ago Rees started refluxing again. He would wake us up at night saying his tummy hurt and point to his chest. He's back on all his meds, but they aren't helping. Tonight, it was absolutely horrible. He was retching, sobbing, screaming!!!!!!!! in pain for over an hour, arching his back, thrashing around in my arms because it hurt so bad. We finally got some meds to stay down. John and I are both panicked and have been sobbing all night. It has brought us back to the worst time in our lives. It was pure h*** and I can't believe it's starting again. So, it looks as if we will be going to the hospital for an emergency Upper GI in the next few days and possibly scheduling him for major surgery to have the Fundo repaired.

Please pray for my Rees. I can't believe this is happening to my baby again. I am absolutely devastated.

Oh, and John looked at me when we finally got Rees to bed tonight and said, "forget going back to school or work. Rees and the kids need you much more than we need money. God has you at home for a reason, and that's where you're staying." Thank goodness I have a fantastic husband who puts the kids above anything else. Needless to say, the whole teaching school thing is on hold for a long while. Rees just is too medically fragile for me to be working full-time and not have the flexibility to be with him.


Denise -- I just read this to my husband, and he's just as touched by it as I am. You hug that precious Rees and know that all your DDA friends are praying for healing and peace for Rees and for you, John, BK and Davis.
 
triplefigs said:
DDA, I could use some serious prayers for Rees (and me) please. Here's some background so you'll understand the seriousness of this issue.

John and I are both panicked and have been sobbing all night. It has brought us back to the worst time in our lives. It was pure h*** and I can't believe it's starting again. So, it looks as if we will be going to the hospital for an emergency Upper GI in the next few days and possibly scheduling him for major surgery to have the Fundo repaired.

Please pray for my Rees. I can't believe this is happening to my baby again. I am absolutely devastated.

Oh, and John looked at me when we finally got Rees to bed tonight and said, "forget going back to school or work. Rees and the kids need you much more than we need money. God has you at home for a reason, and that's where you're staying." Thank goodness I have a fantastic husband who puts the kids above anything else. Needless to say, the whole teaching school thing is on hold for a long while. Rees just is too medically fragile for me to be working full-time and not have the flexibility to be with him.


Oh Denise, I don't have words. :wizard: :wizard: Rees and you must get better. As soon as possible. Hopefully without icky surgury....

I'm so glad that you will have the oppunity to take care of your family yourself. Afterall, no one could do it better. You know them better than anyone. You will be their advocates. they need you. :grouphug: :grouphug: :grouphug: :grouphug:

Hang in there Denise. The road is long, but the reward is great. :love: :cloud9:
 
triplefigs said:
DDA, I could use some serious prayers for Rees (and me) please. Here's some background so you'll understand the seriousness of this issue.

When Rees was born, he was our healthiest until day 2 when he crashed. He was so sick, and the doctor's didn't know if he would make it or not. They could not get him off the ventilator, and it was extremely touch and go. He had horrible time feeding, and was diagnosed with severe reflux (GERD). He literally spent weeks at a time in the hospital, with one stay 45 days just before his first b'day. He vomited up to 40 times per day, was in agony, on all types meds, had so many nasty procedures done it breaks my heart, was on feeding tubes... oh, it was just horrible. We would call the GI doctors at 2am with him screaming in agony, refusing to eat at all, arching his back. We'd end up in the ER, get admitted again, go to the PICU. It was a vicious cycle and some very dark days. Finally at age 17 months he had a major surgery called a Nissen Fundoplication. A Fundo is a drastic and last resort surgery for these kids. They literally go in and wrap the child's stomach around their esophagus to physically prevent any acid for regurgitating out of the stomach. It has lots of side effects, and the kids are unable burp or vomit afterwards, so you must be very careful with stomach flu, food poisoning, swallowing pennies (ok, that is funny). It was MAJOR surgery. He was in the hospital for 10 days, has an incision from his breast bone past his belly button (looks like open heart surgery). Up to that surgery Rees was Failure to Thrive and only weighed 15 pounds. The reflux and long hospital stays and pain are a major reason he is developmentally delayed.

Well, 3 weeks ago Rees started refluxing again. He would wake us up at night saying his tummy hurt and point to his chest. He's back on all his meds, but they aren't helping. Tonight, it was absolutely horrible. He was retching, sobbing, screaming!!!!!!!! in pain for over an hour, arching his back, thrashing around in my arms because it hurt so bad. We finally got some meds to stay down. John and I are both panicked and have been sobbing all night. It has brought us back to the worst time in our lives. It was pure h*** and I can't believe it's starting again. So, it looks as if we will be going to the hospital for an emergency Upper GI in the next few days and possibly scheduling him for major surgery to have the Fundo repaired.

Please pray for my Rees. I can't believe this is happening to my baby again. I am absolutely devastated.

Oh, and John looked at me when we finally got Rees to bed tonight and said, "forget going back to school or work. Rees and the kids need you much more than we need money. God has you at home for a reason, and that's where you're staying." Thank goodness I have a fantastic husband who puts the kids above anything else. Needless to say, the whole teaching school thing is on hold for a long while. Rees just is too medically fragile for me to be working full-time and not have the flexibility to be with him.

My heart breaks for all you guys are going through. I will pray with all my might for you. Would you mind if I shared this with my parents, and had Rees added to their Sunday School's prayer list? Their prayer group seems to do some amazing things. :grouphug:
 
Anyone who wants to add Rees to a prayer list, I would appreciate it. I can PM you our name.
 
triplefigs said:
DDA, I could use some serious prayers for Rees (and me) please. Here's some background so you'll understand the seriousness of this issue.

When Rees was born, he was our healthiest until day 2 when he crashed. He was so sick, and the doctor's didn't know if he would make it or not. They could not get him off the ventilator, and it was extremely touch and go. He had horrible time feeding, and was diagnosed with severe reflux (GERD). He literally spent weeks at a time in the hospital, with one stay 45 days just before his first b'day. He vomited up to 40 times per day, was in agony, on all types meds, had so many nasty procedures done it breaks my heart, was on feeding tubes... oh, it was just horrible. We would call the GI doctors at 2am with him screaming in agony, refusing to eat at all, arching his back. We'd end up in the ER, get admitted again, go to the PICU. It was a vicious cycle and some very dark days. Finally at age 17 months he had a major surgery called a Nissen Fundoplication. A Fundo is a drastic and last resort surgery for these kids. They literally go in and wrap the child's stomach around their esophagus to physically prevent any acid for regurgitating out of the stomach. It has lots of side effects, and the kids are unable burp or vomit afterwards, so you must be very careful with stomach flu, food poisoning, swallowing pennies (ok, that is funny). It was MAJOR surgery. He was in the hospital for 10 days, has an incision from his breast bone past his belly button (looks like open heart surgery). Up to that surgery Rees was Failure to Thrive and only weighed 15 pounds. The reflux and long hospital stays and pain are a major reason he is developmentally delayed.

Well, 3 weeks ago Rees started refluxing again. He would wake us up at night saying his tummy hurt and point to his chest. He's back on all his meds, but they aren't helping. Tonight, it was absolutely horrible. He was retching, sobbing, screaming!!!!!!!! in pain for over an hour, arching his back, thrashing around in my arms because it hurt so bad. We finally got some meds to stay down. John and I are both panicked and have been sobbing all night. It has brought us back to the worst time in our lives. It was pure h*** and I can't believe it's starting again. So, it looks as if we will be going to the hospital for an emergency Upper GI in the next few days and possibly scheduling him for major surgery to have the Fundo repaired.

Please pray for my Rees. I can't believe this is happening to my baby again. I am absolutely devastated.

Oh, and John looked at me when we finally got Rees to bed tonight and said, "forget going back to school or work. Rees and the kids need you much more than we need money. God has you at home for a reason, and that's where you're staying." Thank goodness I have a fantastic husband who puts the kids above anything else. Needless to say, the whole teaching school thing is on hold for a long while. Rees just is too medically fragile for me to be working full-time and not have the flexibility to be with him.


First of all I think John deserves the husband and father of the day or perhaps week or maybe month or year award. That comment you said he made about you had me crying and I am normally not one to tear up. John is one special guy and you and the kids are very lucky to have him.

Second you deserve the mother of the year award. With everything you have been through and you keep on striving and pushing more and more for your kids. I don't see how you do it.

You and John have been blessed with some special kids and I know that they were given to you for a reason. Keep fighting for them anytime you need to vent, a hug, whatever we will always be her for you and your family.

Third sending hugs and pixie dust to Reese. I know he has not had an easy childhood and I am sorry to hear he is probably going to need more surgery. I hope they can as quickly and possibly make him feel better and that they can get this problem taken care of for a long time. ( I know this probably should have been first but I feel right now that you and John need the pixie dust and well wishes as much as Reese does.)

Third sending hugs and pixie dust to Davis and Brantley Kate. I am sure this is effecting them immensely. Please don't forget to give Reese, Brantley-Kate and Davis lots of hugs and kisses. I know you won't.

Sending hugs, pixie dust and prayers for your whole family.

Becky
 
Thank you all so much for the prayers, PMs, encouragement, and love. I'm still terribly upset, but I do feel your strength and support. I emailed all my friends and church, and I've gotten almost 30 emails in less than an hour. I'm lucky to have such supportive DIS friends and friends here. They all went through this with me the first time, and so they are very upset also. When I was with Rees for that 45 days, they literally brought me lunch and dinner every night in the hospital (he was only 10 months old and I couldn't leave him). They did my laundry, went shopping, came to sit with me. I've got really good support here too. Thanks again for all the prayers. It means the world to me.
 
Welcome to the DDA Shana. Hope you stick around. I look forward to learning more about you.

Becky
 
triplefigs said:
DDA, I could use some serious prayers for Rees (and me) please. Here's some background so you'll understand the seriousness of this issue.

When Rees was born, he was our healthiest until day 2 when he crashed. He was so sick, and the doctor's didn't know if he would make it or not. They could not get him off the ventilator, and it was extremely touch and go. He had horrible time feeding, and was diagnosed with severe reflux (GERD). He literally spent weeks at a time in the hospital, with one stay 45 days just before his first b'day. He vomited up to 40 times per day, was in agony, on all types meds, had so many nasty procedures done it breaks my heart, was on feeding tubes... oh, it was just horrible. We would call the GI doctors at 2am with him screaming in agony, refusing to eat at all, arching his back. We'd end up in the ER, get admitted again, go to the PICU. It was a vicious cycle and some very dark days. Finally at age 17 months he had a major surgery called a Nissen Fundoplication. A Fundo is a drastic and last resort surgery for these kids. They literally go in and wrap the child's stomach around their esophagus to physically prevent any acid for regurgitating out of the stomach. It has lots of side effects, and the kids are unable burp or vomit afterwards, so you must be very careful with stomach flu, food poisoning, swallowing pennies (ok, that is funny). It was MAJOR surgery. He was in the hospital for 10 days, has an incision from his breast bone past his belly button (looks like open heart surgery). Up to that surgery Rees was Failure to Thrive and only weighed 15 pounds. The reflux and long hospital stays and pain are a major reason he is developmentally delayed.

Well, 3 weeks ago Rees started refluxing again. He would wake us up at night saying his tummy hurt and point to his chest. He's back on all his meds, but they aren't helping. Tonight, it was absolutely horrible. He was retching, sobbing, screaming!!!!!!!! in pain for over an hour, arching his back, thrashing around in my arms because it hurt so bad. We finally got some meds to stay down. John and I are both panicked and have been sobbing all night. It has brought us back to the worst time in our lives. It was pure h*** and I can't believe it's starting again. So, it looks as if we will be going to the hospital for an emergency Upper GI in the next few days and possibly scheduling him for major surgery to have the Fundo repaired.

Please pray for my Rees. I can't believe this is happening to my baby again. I am absolutely devastated.

Poor Rees!! I will be praying extra hard for all of the Figs!!
Here's some :grouphug: and pixie dust to help the next couple of days.
 
Steamboat Marti said:
I have finally discovered the ONE flaw of the DDA - we are just too far apart to help our friends when they need us most.

Denise - we would all fly to Atlanta tomorrow if we knew it would help. You are all in our thoughts and prayers. I wish we all lived closer!


I think you nailed it on the head Marti...I know I wanted to run over as soon as I started reading Denise's post!!

This is also why I love the DDA, because I know I am not the only one.
 
Well, you all could have a DDA meet in Atlanta... ;)
 
duckyfordonald said:
Thank you so much for the warm welcome! :goodvibes I have to apologize that I have not read through the 1,000+ pages :blush:, so I don't know the "history" that you all share. But I do look forward to posting more frequently and getting to know each of you better. You seem like such a caring, generous (and I can't forget TALENTED) bunch!!! ::yes::
Blessings, Shana

You will soon be part of the history, Shana. Welcome and jump on in.
 
I second Marti's post - it had me wishing I could stow away in DH's luggage - he has to be in Atlanta for business early next week.

That being said, he also was extremely touched by your story, and he would be more than happy to do anything for you or your family while he's in town!
 
Tinkaroo said:
I second Marti's post - it had me wishing I could stow away in DH's luggage - he has to be in Atlanta for business early next week.

That being said, he also was extremely touched by your story, and he would be more than happy to do anything for you or your family while he's in town!

That's so sweet, but he's a Florida Gator, and the orange would just so clash with all the Crimson! :rotfl:
 
triplefigs said:
That's so sweet, but he's a Florida Gator, and the orange would just so clash with all the Crimson! :rotfl:

:rotfl2: :rotfl: :rotfl2: :rotfl: :rotfl2: :rotfl:

He could always bring the BEST kind of orange with him - BURNT! ;)

He can also do the "yamma jamma" with the best of them...
 
Tinkaroo said:
:rotfl2: :rotfl: :rotfl2: :rotfl: :rotfl2: :rotfl:

He could always bring the BEST kind of orange with him - BURNT! ;)

He can also do the "yamma jamma" with the best of them...

Thanks for the laugh. I needed it. And yes, "Rammer Jammer Yellow Hammer, Give 'em Hell, Alabama!"
 
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