Make a Wish (and other organizations!) - Wish Trippers...UNITE!! Volume 2!

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Becky,
Hi! I am not sure about the MAW buttons...we don't leave for our trip until June. I just noticed that you are from Elkhorn. We live in La Vista, NE just down the road from you!
I hope your family has a wonderful time! I can't wait to hear all of the details!
Mary Anne
 
Ok I am not reading the trip reports because I don't want any of the 'magic' ruined...I ALWAYS have to know everything...so I am trying to loosen up and just let what happens on the trip happen...SO if I don't comment that is why...
 
I hope you have a great time. I have found that having 2 kids with CF, if I don't have something to look forward to life just seems to be too much. I have to have somewhere fun to focus my attention and what is more fun than a trip somewhere?

I just had to reply to this because I also have a child with CF so a feel a sort of bond with other parents with children who have CF. I have two other children who have yet to be tested but I am hoping for the best. I have yet to hear when are trip is going to be but I would love to hear some advice from a mom who knows what my particular concerns are.:worship::worship:
 
I just had to reply to this because I also have a child with CF so a feel a sort of bond with other parents with children who have CF. I have two other children who have yet to be tested but I am hoping for the best. I have yet to hear when are trip is going to be but I would love to hear some advice from a mom who knows what my particular concerns are.:worship::worship:

I'd be happy to help in any way I can. My oldest was diagnoesd at 3 mths and my ds was diagnosed the week after he was born. Because of my dd having it and some of the signs he was showing they did a blood test right after he was born. My 8yo dd had a sweat test at 6 mths, because she didn't show any symptoms, they waited until then and it came back negative.
Ask away and I will answer to the best of my abilities. :)
 

Hi everyone, I'm Nicole and i'm new to this site and i'm still trying to get the hang of so please bear with me. I have posted this once before on a different thread but i forgot where. So here it is again. I'll start with how everything started.

First off I'm a 27yr old separated mom of 3. My kids are Jazmine, 7, Elise, 4, and Elijah, who is 3. Elise is my little miracle. She has been so strong through it all. Let's see.... last year on Wed. May 7th is when Elise first got sick. She was vomiting a lot so I took her to her doctor. They said it was just a stomach virus, she had no fever or any other symptoms and that it will pass in 3-4 days. So I took her home. By Friday she couldn't keep anything down not even water so i took her to the ER. They gave her an IV to hydrate her, did bloodwork, tested for infections, and did x-rays of her stomach. 5 hrs later everything came back normal so they gave her zofran and some sent her home. Saturday she was even worse, now she was just dry heaving all day long so i took her back to ER. They did the same things as before plus an ultrasound of her intestines. Still nothing. We went home again. She is still vomiting, and I don't mean like 1-2 time a day, no now it was 6-7 times a day. Everytime she drank or ate anything she would throw up 5- 15 mins later. On Sunday she slept almost all day long. I would wake her up to try and drink or eat popsicles. Still vomiting.

By then I had no idea what to do. I just let her sleep. Monday morning I got woke her up early to take her back to the ER, before i could even get her dressed she started vomiting up nasty, foul smelling green stuff. When she tired to walk she had no balance and kept falling. I called her father to come take the other kids to school and daycare, then I took her back to the ER. I was not leaving until they found out what was really wrong. So they did a CT and my world crumbled. They told she had several tumors in her brain and a few on her spine. She had never been sick in the whole 3 yrs she'd been alive, only a cold maybe twice a yr. I thought they were dumb and made them get several different doctors. They all said the same thing. So they transferred us to Children's Hospital in DC. She was immediately put in icu. By Wed. she was having seizures. They said that the largest tumors were blocking her spinal fluid from draining which was causing pressure on her brain. That's what was causing all her symptoms. They put a drain (a shunt that's on the outside) in her head. A couple days later they took the drain out, did a biopsy, and put in a permanant shunt. She was diagnosed with Primitive neuroectodermal tumors (PNET). I was going crazy with worry and stress. Everything was happening so fast. I still couldn't get a grip on anything. When she came out of surgery she was worse. Now she couldn't even move her legs or sit up without help. Now i'm like Lord what did they do to my baby! They did another MRI and said it was caused from all the pressure and that she regain her mobility back in time.

Next they put in a double lumen broviac so she could start her chemo. Now that was just terrible. She had 6 rounds of high dose chemo with stem cell replacement. She had terrible side effects. On the night of her 1st day of chemo she got really sick, she became non-responsive to everything, and her eyes rolled around in her head, you know i was in a panic. they rushed her to icu again and gave her some meds. They added triple the amount of sodium to her fluids from then on. Throughout her chemo she had mouth sores, hair loss, nausea and vomiting, and severe diarrhea, she wouldn't eat, infections, headaches, pain.... It was really bad. They put in a feeding tube plus she would get blood and platelets every week, sometimes twice a week. It was horrible. She was also extremely tired and wanted to sleep all the time, which was hard because she had PT and OT each 2x a day. We spent the entire 6 months in the hospital. But through it all she was as sweet as can be, and when she was up to it she fell in love with painting. I also tried to get her to play anything that i thought would make her happy. She always tired to perk up when the family came over. She was and is still a strong child.

She had about a 3wk break after chemo before her radiation. By that time we got her walking again and she was even running a little and her feeding tube was now gone. Her balance was almost completely back too. Next was radiation, Mon-Fri. for 2 1/2 months. Her radiation went smoothly, her side effects was mild. She just ended her mandatory 3 mth break and has recovered almost fully from everything. She still has a few small tumors left and just started a low dose oral chemo regiment (she gets to be home this time that she will be on for the next 6 months. She has been blessed to have made it this far!!! The doctors told us in the beginning that she would have a 5% chance of beating this cancer. But I thank the Lord because she is here and doing good!!!

MAW has granted her wish to see Cinderella. We are going to WDW in May and will be staying at GKTW. We are all excited. It is a well needed vacation for all of us. I do have a question. My kids and I live with my parents plus my 12 yr old nephew. MAW is paying for me and my 3 kids, and since i'm a single mother they are also paying for my mother to go too. I have been looking for a vacation package that is the same that GKTW gives that is affordable for my dad and nephew so that they can enjoy everything that we get to. So i haven't any luck. Does anybody have any suggestions? Thanks

Also i'm trying to start planning an itinerary for the trip but i have no idea where to start. I have read some great tips from the posts and know some of the things i want to put on it. Any thoughts on what to do 1st and what days are better to do certain things? We arrive at MCO at 10:20am on Tues. May 5, 2009 and we depart at 2:55pm on Monday May 11, 2009. Any suggestions would be greatly appreciated.

Sorry this is so long. But I always tell everything so people can know just how far Elise has made it with God's help. I will try and load some pics of the family. Thank you to everyone who reads about Elise's journey and to everyone in advance who replys to this post, and to anyone who already has.
 
Hi everyone!
So glad that I found you! I've spent the last few nights (staying up all hours) Googling "Disney World Make A Wish Trips", and that's how I found this forum. I have to be honest my eyes are tired from trying to read all the great trip reports and advice. I am the type of person who really needs to prepare and wants to do as much research as possible...So I need some HELP, please!!
First, I should introduce my family: there is our beautiful wish child Azaria (her name is pronounced like the word area with an Az in front of it). She is 6 years old and was diagnosed with Aicardi Syndrome at birth. (Aicardi Syndrome consists of daily seizures, the absence of the center part of the brain, retinal lesions that cause blindness, and developmental delays). She does not speak, but tries to communicate in her own way. She is unable to sit unassisted and is unable to stand or walk. We were told her life expectancy is 5-10 years. Azaria has about 8-12 seizures a day, and about once a month she requires medical intervention to stop them. BUT she is doing extremely well, given all that. She is a very happy and precious child!

Our son Aidan is 4 and will turn 5 on the trip, May 12! He is such a sweet little guy and loves his "sissy" so much. He tries to care for her during her seizures, saying "it's ok sissy" while holding her hand or stroking her head. Aidan has a very severe peanut allergy, we almost lost him when he was 2, due to an exposure to peanut butter. We are very careful with Aidan and carry epinephrine with us at all times.

We also have an older son, Christopher, he just turned 21. He lives near San Francisco but comes home often. Christopher is really the only person who helps us care for the kids, he is our only respite. And the kids adore their big brother.

Then there is me and my husband. I'm Debi, and my husband is TJ, we live in Central California. We have annual passes to Disneyland and visit often, especially when we take Azaria to UCLA.

That's us, now where to begin??? Azaria's wish was granted in June of last year. We've been trying to take this trip since then but could never seem to work out the dates. So I called MAW in January and gave dates that we would be available to go in February or March. Never heard back so I called back a couple of weeks ago and our wish rep was so sorry she never got back to us. I guess she kind of dropped the ball. No problem though, we gave her new dates for May and she set it up the next day.

We leave Thursday May 7th on American Airlines at 7:00am. We connect in Dallas to Orlando, arriving at 7:10pm. Initially we were to fly home on the 13th but I asked if we could extend our stay at our own expense, so now we are leaving on Sunday, May 18 at 4:40pm, arriving home at 9:40pm.
(I haven't planned what we will do or where we will stay those extra days but thought the extra time would help us not feel so rushed.)

I would really like some help planning a day to day itinerary. I could really use some help here, my computer research time is only at night when I can barely even think clearly, and Disney World seems so foreign to me.

Things Azaria would like: character meet & greets, "kiddie rides", shows, and she loves animals, specifically dolphins! I thought a visit to Animal Kingdom would be in order, if tickets are available for that park. Seaworld would also be a must. As a family, we just love to hang out together, enjoy shows, we think Azaria would love the Cirque du Soliel show La Nouba, and any other shows. She loves lights and interaction with characters, parades, fireworks.

We will be there on Aidan's birthday, on the 12th he will be 5. We want to do something so that he feels special on his birthday, so we were thinking of taking him to the Kennedy Space Center since he loves spaceships and astronauts. Are tickets given to the space center? I just read online that on May 12th, they are launching Space Shuttle Atlantis. This is something I need to look into more to see if we could view the launch from the beach or somewhere nearby.

Well I should really get some sleep because I am starting to ramble and this is getting really long! I know I will have lots of questions and will begin writing my lists, schedules and plans tomorrow. Again, any help/input would be great.

One last thing, unfortunately MAW is not paying for our son Christopher to come with us, I'm disappointed although I understand. If there are any suggestions on getting his flight or Disney tickets cheap, PLEASE let me know. His one way ticket there on our flight is $300 right now. He is flying back early on the 14th and I can get that ticket for about $100, but with adding the tickets to the parks, it is going to be expensive and we just don't know how we are going to pay for it. I was told he can stay with us at GKTW but don't know what is included with that? Food? Possibly tickets too?

Thank you so much! I look forward to getting to know you all. I feel like I know some of you already since I've been reading your posts and trip reports!

Thanks again, and sorry this first post is so long!

Blessings,
Debi
 
I was wondering if anyone has a tip on how to wear the GKTW button without making big holes in their kids' shirts. We have several holiday buttons/pins that Sam usually wears to school on the holiday. It never fails, he pulls on the pin and ends up with huge holes in his shirts. If he buys some cute t-shirts at Disney, I don't want him to come back with shirts that look like swiss cheese!
Can you pin it to a lanyard or something? Will it still be visible enough? Am I the only person who has ever had this issue??
Mary Anne
 
I did not see this on the thread already...

Please pray for Noah and his family!

He began coughing up blood at home. Nichole called 911 and they, after hearing of his condition, sent paramedics AND a helicopter to get Noah. The helicopter was in town because of some flooding. They blocked the highway to pick up the little guy. :hug:

He was then air lifted to the hospital in 4 minutes.

He is now in the PICU with a pulmonary hemmorhage.

Please pray for his entire family.



www.noahgrantjohn.blogspot.com
 
Hi everyone, I'm Nicole and i'm new to this site and i'm still trying to get the hang of so please bear with me. I have posted this once before on a different thread but i forgot where. So here it is again. I'll start with how everything started.

MAW has granted her wish to see Cinderella. We are going to WDW in May and will be staying at GKTW. We are all excited. It is a well needed vacation for all of us. I do have a question. My kids and I live with my parents plus my 12 yr old nephew. MAW is paying for me and my 3 kids, and since i'm a single mother they are also paying for my mother to go too. I have been looking for a vacation package that is the same that GKTW gives that is affordable for my dad and nephew so that they can enjoy everything that we get to. So i haven't any luck. Does anybody have any suggestions? Thanks

Also i'm trying to start planning an itinerary for the trip but i have no idea where to start. I have read some great tips from the posts and know some of the things i want to put on it. Any thoughts on what to do 1st and what days are better to do certain things? We arrive at MCO at 10:20am on Tues. May 5, 2009 and we depart at 2:55pm on Monday May 11, 2009. Any suggestions would be greatly appreciated.

Sorry this is so long. But I always tell everything so people can know just how far Elise has made it with God's help. I will try and load some pics of the family. Thank you to everyone who reads about Elise's journey and to everyone in advance who replys to this post, and to anyone who already has.

I'm glad you found this thread!!!! There are so many people here that can give you suggestions and help you plan. I'm sure Elise would love to eat at Cinderella's Royal Table. There is a meet and greet with Cinderella before you eat and during dinner you get to meet some other very special princesses. Another place you can try is 1900 Park Fair. This buffet is in the Grand Floridian Hotel which is a short ride from Magic Kingdom on the monorail. You get to meet Cinderella, the stepmother, the stepsisters, and the prince.

I think Maroo (or someone here) has a planning spreadsheet she can email to you. We haven't been to GKTW yet, so I can't help you too much with that. But your in the right spot!!

I'm glad to hear that Elise is doing better. You guys will have a great time in Disney!!!!!!!:goodvibes

Tim
 
I was wondering if anyone has a tip on how to wear the GKTW button without making big holes in their kids' shirts. We have several holiday buttons/pins that Sam usually wears to school on the holiday. It never fails, he pulls on the pin and ends up with huge holes in his shirts. If he buys some cute t-shirts at Disney, I don't want him to come back with shirts that look like swiss cheese!
Can you pin it to a lanyard or something? Will it still be visible enough? Am I the only person who has ever had this issue??
Mary Anne

They provide you with a lanyard, that you can put it on. This also holds some of the passes you will use. No need to pin it to a shirt.
 
Hi everyone, I'm Nicole and i'm new to this site and i'm still trying to get the hang of so please bear with me. I have posted this once before on a different thread but i forgot where. So here it is again. I'll start with how everything started.

Hey Nicole,
Welcome to the site. Your daughter is indeed a miricle and had me in tears for most of your post. I so glad that she is doing better and glad that she is able to go on a wish trip.
 
Juliana and I will be saying a prayer for Noah. They have been through so much, I hope he is OK.
 
Hi everyone, I'm Nicole and i'm new to this site and i'm still trying to get the hang of so please bear with me. I have posted this once before on a different thread but i forgot where. So here it is again. I'll start with how everything started.

Welcome to the Wish Trippers thread!! You have certainly come to the right place. :)

MAW has granted her wish to see Cinderella. We are going to WDW in May and will be staying at GKTW.

Bless your heart!!! It sounds like she has been such a trooper and I am so glad that her wish is being granted!!! :banana: :banana: :banana: And you have been through so much. I am so sorry. :hug:



I have been looking for a vacation package that is the same that GKTW gives that is affordable for my dad and nephew so that they can enjoy everything that we get to. So i haven't any luck. Does anybody have any suggestions? Thanks

I think you DID post on this thread!! Your answer to this question was answered by Noah's Mom, who is also named Nichole (but spells it with an h).

Let me see if I can find her answer...Her answer is in blue...if I can get this to work... And you have lots more answers, too, on page 81 of this thread.

Another good reputable site for discounted tickets is http://www.undercovertourist.com. Also, if you register at http://www.mousesavers.com, you will get their newsletter that gives you a special link to undercovertourist that will discount the tickets even more! Mousesavers also has some great discounts to hotels on their website.

I also just recently found out about Windsor Hills (from these boards of course!). This website http://www.vacationcentralflorida.com has beautiful condos that rent for $299-$399 a week. Lots of people on this board have used them. Might even be cheaper than a hotel!


Also i'm trying to start planning an itinerary for the trip but i have no idea where to start. I have read some great tips from the posts and know some of the things i want to put on it. Any thoughts on what to do 1st and what days are better to do certain things? We arrive at MCO at 10:20am on Tues. May 5, 2009 and we depart at 2:55pm on Monday May 11, 2009. Any suggestions would be greatly appreciated.

I can help you with this and I will send you a PM to get some info from you and hopefully help you specifically plan some stuff. Feel free to ask questions here, too!!!

Generally your first day will be spent traveling, enjoying GKTW, getting settled in your Villa and doing the GKTW orientation where they tell you about the Village and give you your tickets and everything. There are lots of wonderful things to do at the Village. Make sure you don't miss the playground! :)


Welcome to the Wish Trippers thread!! :) Feel free to ask more questions!!!
 
Hi everyone!
So glad that I found you! I've spent the last few nights (staying up all hours) Googling "Disney World Make A Wish Trips", and that's how I found this forum. I have to be honest my eyes are tired from trying to read all the great trip reports and advice. I am the type of person who really needs to prepare and wants to do as much research as possible...So I need some HELP, please!!
First, I should introduce my family: there is our beautiful wish child Azaria (her name is pronounced like the word area with an Az in front of it). She is 6 years old and was diagnosed with Aicardi Syndrome at birth. (Aicardi Syndrome consists of daily seizures, the absence of the center part of the brain, retinal lesions that cause blindness, and developmental delays). She does not speak, but tries to communicate in her own way. She is unable to sit unassisted and is unable to stand or walk. We were told her life expectancy is 5-10 years. Azaria has about 8-12 seizures a day, and about once a month she requires medical intervention to stop them. BUT she is doing extremely well, given all that. She is a very happy and precious child!

Our son Aidan is 4 and will turn 5 on the trip, May 12! He is such a sweet little guy and loves his "sissy" so much. He tries to care for her during her seizures, saying "it's ok sissy" while holding her hand or stroking her head. Aidan has a very severe peanut allergy, we almost lost him when he was 2, due to an exposure to peanut butter. We are very careful with Aidan and carry epinephrine with us at all times.
Welcome Debi!!!! I am so glad that you are finally able to go on Azaria's Wish trip. I am sure you will have a great time. It is great that your son is going to be turning 5 on your trip. There is a great program at Disney Parks to get in free on your birthday. But since he will already have a ticket to the Park they offer two other deal. You can chose the Ultimate Fast Pass (but you wont have to because from my understanding MaW and GKTW buttons you will not need this) or a gift card to use at the Disney Park that will equal the price you would have paid for a One day park pass for Aidan.

I also wanted to say hey because I also have an Aidan. He is 21 months old and as cute as a button.
 
I was wondering if anyone has a tip on how to wear the GKTW button without making big holes in their kids' shirts. We have several holiday buttons/pins that Sam usually wears to school on the holiday. It never fails, he pulls on the pin and ends up with huge holes in his shirts. If he buys some cute t-shirts at Disney, I don't want him to come back with shirts that look like swiss cheese!
Can you pin it to a lanyard or something? Will it still be visible enough? Am I the only person who has ever had this issue??
Mary Anne

I'm with macntosh. My son does the same thing with pins, so, either I wore the pin, or we put it on the lanyard. Your GAC is what will get you extra consideration on the attractions. I wore that as well, because Adam would have destroyed it (paper tucked into a plastic pouch.) The CM's would always defer to the person with the GAC to ask "how many in your party"..."do you want a wheelchair accessible car/boat". The GKTW button gets you to the front of the line with character meetings, but we didn't do any of those.

~Elisa
 
Hi everyone!
So glad that I found you! I've spent the last few nights (staying up all hours) Googling "Disney World Make A Wish Trips", and that's how I found this forum.
Debi

Oh gosh...we made Google! :yay:

I am the type of person who really needs to prepare and wants to do as much research as possible...So I need some HELP, please!!


You have come to the right place!! :)


Our son Aidan is 4 and will turn 5 on the trip, May 12! He is such a sweet little guy and loves his "sissy" so much. He tries to care for her during her seizures, saying "it's ok sissy" while holding her hand or stroking her head. Aidan has a very severe peanut allergy, we almost lost him when he was 2, due to an exposure to peanut butter. We are very careful with Aidan and carry epinephrine with us at all times.

Wow...you have your hands full. I am sorry for all of the illness...but I am so glad you are going to Disney on a Wish Trip!!

Disney is very good about allergies. You will probably be pleasantly surprised how well he does. Make sure to tell the folks at GKTW, too, that he is allergic to peanut butter.


We also have an older son, Christopher, he just turned 21. He lives near San Francisco but comes home often. Christopher is really the only person who helps us care for the kids, he is our only respite. And the kids adore their big brother.

I THINK that they will probably let Christopher and your father stay with you at GKTW in your villa. If you think they will fit with the room that you will have.

Otherwise, you can just get a hotel room close by, and just spend most of your time in the villa and sleep in the hotel nearby.

GKTW will let you "buy" food tickets for Christopher and your father to eat. They are $1.00 per meal. It is also possible that they will just let them eat with you for free, too!

Honestly, if I was taking the trip...I would just go down there and then find a hotel in the area that looks like something you would like just to let them sleep. That way, you won't have to worry about paying for a hotel you did not need if they let them stay with you at the villa! :)


Then there is me and my husband. I'm Debi, and my husband is TJ, we live in Central California. We have annual passes to Disneyland and visit often, especially when we take Azaria to UCLA.

That's us, now where to begin??? Azaria's wish was granted in June of last year. We've been trying to take this trip since then but could never seem to work out the dates. So I called MAW in January and gave dates that we would be available to go in February or March. Never heard back so I called back a couple of weeks ago and our wish rep was so sorry she never got back to us. I guess she kind of dropped the ball. No problem though, we gave her new dates for May and she set it up the next day.

We leave Thursday May 7th on American Airlines at 7:00am. We connect in Dallas to Orlando, arriving at 7:10pm. Initially we were to fly home on the 13th but I asked if we could extend our stay at our own expense, so now we are leaving on Sunday, May 18 at 4:40pm, arriving home at 9:40pm.
(I haven't planned what we will do or where we will stay those extra days but thought the extra time would help us not feel so rushed.)

I would really like some help planning a day to day itinerary. I could really use some help here, my computer research time is only at night when I can barely even think clearly, and Disney World seems so foreign to me.

Things Azaria would like: character meet & greets, "kiddie rides", shows, and she loves animals, specifically dolphins! I thought a visit to Animal Kingdom would be in order, if tickets are available for that park. Seaworld would also be a must. As a family, we just love to hang out together, enjoy shows, we think Azaria would love the Cirque du Soliel show La Nouba, and any other shows. She loves lights and interaction with characters, parades, fireworks.

We will be there on Aidan's birthday, on the 12th he will be 5. We want to do something so that he feels special on his birthday, so we were thinking of taking him to the Kennedy Space Center since he loves spaceships and astronauts. Are tickets given to the space center? I just read online that on May 12th, they are launching Space Shuttle Atlantis. This is something I need to look into more to see if we could view the launch from the beach or somewhere nearby.

Well I should really get some sleep because I am starting to ramble and this is getting really long! I know I will have lots of questions and will begin writing my lists, schedules and plans tomorrow. Again, any help/input would be great.

One last thing, unfortunately MAW is not paying for our son Christopher to come with us, I'm disappointed although I understand. If there are any suggestions on getting his flight or Disney tickets cheap, PLEASE let me know. His one way ticket there on our flight is $300 right now. He is flying back early on the 14th and I can get that ticket for about $100, but with adding the tickets to the parks, it is going to be expensive and we just don't know how we are going to pay for it. I was told he can stay with us at GKTW but don't know what is included with that? Food? Possibly tickets too?

Thank you so much! I look forward to getting to know you all. I feel like I know some of you already since I've been reading your posts and trip reports!

Thanks again, and sorry this first post is so long!

Blessings,
Debi

Oh my gosh!!!! That is SOOOOOO cool!! He could actually go watch the shuttle go off on his birthday?!?!?! Wow.

They do give tickets to Kennedy Space Station. I am not sure if Christopher and you father would have to buy separate tickets, though. :confused3

I will be glad to help you with a planner...it should sorta guide you on the parks.

Oh...it looks like they said that Christopher can stay with you. I would think your father can too...

They won't include tickets for the two of them. I don't know much about getting cheap tickets...sounds like getting the best day will be the most beneficial. Try to let him fly with you to get down there, though, as there is a lot of special stuff he would miss if he flew down a day later or something.



Here is some information from Noah's Mom, Nichole...about getting cheap tickets...

Another good reputable site for discounted tickets is http://www.undercovertourist.com. Also, if you register at http://www.mousesavers.com, you will get their newsletter that gives you a special link to undercovertourist that will discount the tickets even more! Mousesavers also has some great discounts to hotels on their website.

I also just recently found out about Windsor Hills (from these boards of course!). This website http://www.vacationcentralflorida.com has beautiful condos that rent for $299-$399 a week. Lots of people on this board have used them. Might even be cheaper than a hotel!
 
I was wondering if anyone has a tip on how to wear the GKTW button without making big holes in their kids' shirts. We have several holiday buttons/pins that Sam usually wears to school on the holiday. It never fails, he pulls on the pin and ends up with huge holes in his shirts. If he buys some cute t-shirts at Disney, I don't want him to come back with shirts that look like swiss cheese!
Can you pin it to a lanyard or something? Will it still be visible enough? Am I the only person who has ever had this issue??
Mary Anne

I think everyone else said this too...you can definitely pin it on your lanyard...

My only word of advice is to completely poke it through the lanyard. We lost our button - which is totally not cool - because we just put it on a lanyard without poking it through the lanyard string.
 
I'd be happy to help in any way I can. My oldest was diagnoesd at 3 mths and my ds was diagnosed the week after he was born. Because of my dd having it and some of the signs he was showing they did a blood test right after he was born. My 8yo dd had a sweat test at 6 mths, because she didn't show any symptoms, they waited until then and it came back negative.
Ask away and I will answer to the best of my abilities. :)

Unfortunatly my son wasn't diagnosed until he was 6. Looking back he definatly had symptoms but not knowing anything about CF I couldn't see it and since he (Thank God) hasn't had any huge medical complications it was easy to ignore some of the smaller stuff.

I didn't even know about CF until I was told I was a carrier when I was Pregnant with Aidan. I did a little research than but since had no problems at birth I kind of just forgot about it. That was until August of last year when Liam got a cough that wouldn't go away. It was not the first time so I wanted to get to the bottom of it. I kept getting no answers so I took it on myself to do research and found CF. It got my intrest because I knew I was a carrier. I looked at the symptoms and suddenly everything made sense. Him being small and thin for his age, his extremly large BM, I even started looking at his finger nails for clubbing and licked his skin to see if it was salty.:lmao::lmao:

I told his pediatician of my suspicions and unfortunatly he basicly called my a hypercondriac(not sure of spelling) but gave me the sweat test even though he thought is was a waste of medical resorces. It took me three months of three sweat tests (borderline high but it turned out they don't do the test right) and one blood test to find out that he has a double mutation but his dr is still telling me he didn't have it. I pushed on and found a CF dr who looked at the same piece of paper and told me that he does.

Now I just have to get the other two tested, been hard becausre I used all my time to get Liam to all his tests and I am a single mom. They don't have is symptoms though, but it doesn't stop my worring.

Gee, I didn't mean to write this much. :eek:
 
Hi everyone, I'm Nicole and i'm new to this site and i'm still trying to get the hang of so please bear with me. I have posted this once before on a different thread but i forgot where. So here it is again. I'll start with how everything started.

MAW has granted her wish to see Cinderella. We are going to WDW in May and will be staying at GKTW. We are all excited. It is a well needed vacation for all of us. I do have a question. My kids and I live with my parents plus my 12 yr old nephew. MAW is paying for me and my 3 kids, and since i'm a single mother they are also paying for my mother to go too. I have been looking for a vacation package that is the same that GKTW gives that is affordable for my dad and nephew so that they can enjoy everything that we get to. So i haven't any luck. Does anybody have any suggestions? Thanks

Also i'm trying to start planning an itinerary for the trip but i have no idea where to start. I have read some great tips from the posts and know some of the things i want to put on it. Any thoughts on what to do 1st and what days are better to do certain things? We arrive at MCO at 10:20am on Tues. May 5, 2009 and we depart at 2:55pm on Monday May 11, 2009. Any suggestions would be greatly appreciated.

Sorry this is so long. But I always tell everything so people can know just how far Elise has made it with God's help. I will try and load some pics of the family. Thank you to everyone who reads about Elise's journey and to everyone in advance who replys to this post, and to anyone who already has.

I am sorry to hear all that your daughter has had to go through, but am glad to hear that she is doing well know. Love her first name, by the way. ;) I remember you posting the first time, because I remember the part about your Dad and your nephew. I found you on page 80 of this thread, and I wrote something short back on page 81. MAW may not be paying your dad and nephew's way, but they still may be able to stay at GKTW with you. Call GKTW tell them that you live with them and ask if they can stay with you in the villa. The villa can sleep 7 (we did it). There is a master bedroom (king size bed) a kids' room (two twins) a queen sized fold out sofa, a twin bed roll away and a crib. GKTW may ask MAW to verify that they are "residents". I don't know about the ticket packages though. I don't think MAW pays for those, I think the parks donate them...GKTW may be able to help you, but if not, try mousesavers.com and allears.net for advice on good places to buy inexpensive tickets.

Make sure you spend some time at the kidcot stations at Epcot if Elise loves to paint. She can get masks from various countries and decorate them in craft centers...that may be right up her alley! The other thing that is neat is the face painting. I saw them set up at AK, but I know they are other places as well. They paint animal faces or butterflies and I think it is under $20.

Please continue to ask any questions you might have...

~Elisa
 
Thanks for the welcome. We leave home June 22 and return June 28. I didn't realize that there were character breakfasts at Universal. That sounds great! Sam is our wish kid and LOVES Spiderman and ALL Dr. Seuss. My girls are out of the princess stage anyway. And Sam prefers super heroes above all. That sounds right up our alley.
We are very excited about this trip. I am just nervous because I am SUCH a last minute person, I don't plan anything. I think it comes with the territory of having a kid who is perfectly fine one minute and having seizures the next. It seems like any time we plan anything that is when the seizures strike...
But I do know that we could get a lot more out of this trip if we don't fly by the seat of our pants. So I really am going to try!
Mary Anne

Merneric:

Sorry I didn't see this earlier. My son LOVES Spiderman too. It was the highlight for him; that and Indiana Jones and Star Tours. There really is no problem with going with the flow and not over obsessing. I think the most important thing to remember is that there are time constraints and as a result it is not possible to do everything. Trying will only make you miserable. I think the only thing you really need to plan are the things that are "must do" for your family. From there, you may want to talk to Maroo about the best days to do which parks. There is a service called Tour Guide Mike where you can type in the days you are traveling and they give you advice on which day to do which park, etc. Maroo does this too for wish families (and it is free not $19.95.) Even if you do know which day you want to do which park, you may alter it when you are there because of weather...just try and be flexible with a "rough draft" of what you want to do, and you will enjoy yourself much more.

I understand how seizures can disrupt your family plans. We deal with the same thing here. I think that my other children are much more empathetic with special needs kids than most children their age, because of their exposure to their brother. Let us know if you have any more questions.

~Elisa
 
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