Help from parents of children with anaphylaxis

quandrea

DIS Veteran
Joined
Jun 24, 2010
Messages
6,147
My daughter, 2 has just been diagnosed with a peanut allergy, level 3. How will we fair at WDW? Can she have snacks from the vendors, bakeries, etc. What do the sit down restaurants do for us. Are CS restaurants safe? She is supposed to avoid peanuts and all may contains. She carries an epipen jr. Any advice will be helpful. Feeling scared/overwhelmed.
 
go over to the disabilities board. There is a lot of info over there. I think there may even be a sticky about dealing with allergies at Disney. I know they have lists of foods and contact info at Disney on that board.
 
My son, age 5, has severe anaphylactic peanut and tree nut allergies as well. We always carry epi-pen to the parks(and through the airport) with no issues. Always let your server at TS restaurants know your issue and a chef will come and walk you through the menu/ buffet. At CS places just ask for the "book" of ingredients, every place has one. Disney is a great place to travel to with this problem, so much easier than dealing with it " in the real world". We have never had any issues with my son and we go every year. Have fun and try to enjoy yourself. The disabilities threads are great, so start there. You are definitely not alone in this. Have a wonderful time:thumbsup2
 

We found out DD5 was peanut and tree nut allergic just before our last trip. She had a horrible reaction to some pesto that shaved a few years off my life. The allergist was shocked we'd never been to the ER for this for her before b/c she's so highly allergic. I had the allergy info added to all of our ADRs. Each restaurant was different, but there was always special attention given to the allergy. In many cases, the chef came to our table to discuss allowable foods/give me a tour of the buffet, anything special they could do (offered to get me safe donuts or breads), etc. If you've already made your ADRs, call and have them add it too all of them.

We didn't do a ton of CS last trip, but we did utilize CS for snacks here and there. The standout moment was at Starring Rolls...they wouldn't serve her anything out of the case and didn't feel any of the cupcakes were safe, but they found her a brownie in the back that was OK for her to consume.

I am also happy to report that she didn't have a single reaction the entire trip. :woohoo:

DD5 also wears a medical alert bracelet when in the park...i.e. in case she gets lost they will know about her allergy before trying to feed her anything.

I have to say that I'm pretty nervous about CS for her just b/c there's just not as much you can control, so right now I have 2 TS per day planned. However, I know from reading other people's posts, the CS spots are pretty well versed in allergies. I read about one woman getting a kids meal for her child at Casey's and a CM ran to an area on MSUSA just so he could have a safe dessert with his meal.

Definitely check out DisAbilities as there is a lot of helpful info on there as well. :goodvibes
 
Our DS is 5.He was diagnosed at 23 months after testing.He is considered anaphylaxis to peanuts and has a less severe egg allergy that allows for eggs within baked goods. We travel often with DS including WDW. WDW is very careful with allergies but you need to know what you are looking for. Most baked goods and desserts are going to be off limits as most are made out of the facility and they will not guarantee safety of them. The only dessert we allowed DS was soft serve ice cream and ice pops. At sit downs, the chief will come out before any food, including the bread basket is brought to your table and talk with you. For us, we avoid most baked goods and dessert and avoid most Asian foods. We avoid all contains, many contain, may contain traces, made on the same equipment BUT we do allow made in the same facility. Our doctor oked this for US. A few places I have asked the chief if he would read the exact wording on a package to see if we were comfortable with the food. Some would, other preferred we avoid it all together. We tend to buy snacks, bagged and labeled in gift shops and we were good with many items. We allow the pop corn but I am not sure what the warning on it may be. At CS we just avoid the dessert and any Asian places and we have always been ok. The asian place may be ok, but we have never tried anywhere except out local place where they know DS by name::yes::.

Epi-pen is no problem. You are going to have a diaper bag anyway with a toddler. We are NEVER without our pen. We travel with at least four but do not carry all of them into the parks. Know your child's protocol for benedryl and carry that if needed. We keep the single teaspoon packs.

Always carry snacks and treats for when she can not have what is available. For CS, we would take our dessert (never anything that had peanuts, but often a "may contain warning") out of the restaurant and purchase DS one of the pop-ice things he loved and eat dessert together.

In the big picture, PA are sometimes more scary that some other allergies, but often really much easier to handle once you are good at it!

Hugs and prayers, you will be fine!
 
We found out DD5 was peanut and tree nut allergic just before our last trip. She had a horrible reaction to some pesto that shaved a few years off my life. The allergist was shocked we'd never been to the ER for this for her before b/c she's so highly allergic. I had the allergy info added to all of our ADRs. Each restaurant was different, but there was always special attention given to the allergy. In many cases, the chef came to our table to discuss allowable foods/give me a tour of the buffet, anything special they could do (offered to get me safe donuts or breads), etc. If you've already made your ADRs, call and have them add it too all of them.

We didn't do a ton of CS last trip, but we did utilize CS for snacks here and there. The standout moment was at Starring Rolls...they wouldn't serve her anything out of the case and didn't feel any of the cupcakes were safe, but they found her a brownie in the back that was OK for her to consume.

I am also happy to report that she didn't have a single reaction the entire trip. :woohoo:

DD5 also wears a medical alert bracelet when in the park...i.e. in case she gets lost they will know about her allergy before trying to feed her anything.

I have to say that I'm pretty nervous about CS for her just b/c there's just not as much you can control, so right now I have 2 TS per day planned. However, I know from reading other people's posts, the CS spots are pretty well versed in allergies. I read about one woman getting a kids meal for her child at Casey's and a CM ran to an area on MSUSA just so he could have a safe dessert with his meal.

Definitely check out DisAbilities as there is a lot of helpful info on there as well. :goodvibes

I've also gotten a medical alert bracelet. I just want anyone coming across her without me to know about the allergy. I figured that bakeries and candy shops will be more dangerous--at WDW and outside of the world. Not a huge loss because I'm an avid baker.
 
Our DS is 5.He was diagnosed at 23 months after testing.He is considered anaphylaxis to peanuts and has a less severe egg allergy that allows for eggs within baked goods. We travel often with DS including WDW. WDW is very careful with allergies but you need to know what you are looking for. Most baked goods and desserts are going to be off limits as most are made out of the facility and they will not guarantee safety of them. The only dessert we allowed DS was soft serve ice cream and ice pops. At sit downs, the chief will come out before any food, including the bread basket is brought to your table and talk with you. For us, we avoid most baked goods and dessert and avoid most Asian foods. We avoid all contains, many contain, may contain traces, made on the same equipment BUT we do allow made in the same facility. Our doctor oked this for US. A few places I have asked the chief if he would read the exact wording on a package to see if we were comfortable with the food. Some would, other preferred we avoid it all together. We tend to buy snacks, bagged and labeled in gift shops and we were good with many items. We allow the pop corn but I am not sure what the warning on it may be. At CS we just avoid the dessert and any Asian places and we have always been ok. The asian place may be ok, but we have never tried anywhere except out local place where they know DS by name::yes::.

Epi-pen is no problem. You are going to have a diaper bag anyway with a toddler. We are NEVER without our pen. We travel with at least four but do not carry all of them into the parks. Know your child's protocol for benedryl and carry that if needed. We keep the single teaspoon packs.

Always carry snacks and treats for when she can not have what is available. For CS, we would take our dessert (never anything that had peanuts, but often a "may contain warning") out of the restaurant and purchase DS one of the pop-ice things he loved and eat dessert together.

In the big picture, PA are sometimes more scary that some other allergies, but often really much easier to handle once you are good at it!

Hugs and prayers, you will be fine!

What a lovely post. Thank you. I have an appt with the doctor to go over some questions I have gathered over the past few days. I want to know how many epi pens we need for travel (for example, we have a five hour flight booked for September). He told me one epi pen was plenty, but the school wanted two. I think I'm more comfortable with two on hand myself. I'm glad to hear from others that they'll bring out safe donuts. It's the one dessert my dd loves. Our famous donut shop here in Canada, tim Hortons, is not peanut free. My dd has probably eaten a thousand of their donut holes but I guess I'll have to find a substitute from here on in. It's her one indulgence.
 
What a lovely post. Thank you. I have an appt with the doctor to go over some questions I have gathered over the past few days. I want to know how many epi pens we need for travel (for example, we have a five hour flight booked for September). He told me one epi pen was plenty, but the school wanted two. I think I'm more comfortable with two on hand myself. I'm glad to hear from others that they'll bring out safe donuts. It's the one dessert my dd loves. Our famous donut shop here in Canada, tim Hortons, is not peanut free. My dd has probably eaten a thousand of their donut holes but I guess I'll have to find a substitute from here on in. It's her one indulgence.

I don't advise ever going anywhere with only one Epi Pen. The Epi Pen only buys you time until paramedics can arrive, so if they take longer than 15 min to get to you, you may need another dose of epi. Also, what if one pen malfunctions or something else happens to one of the pens? Better safe than sorry and always have two.

I bring 6 Epi Pens for my DD when we travel. I'm sure it's overkill, but it's what makes me feel comfortable, so that's what I do. Once you decide on how many to bring, be sure to pack all of them (as well as Benadryl and any other meds your DD may need) in your carryon. Never put those meds in your checked luggage.

As others have mentioned, you need to ask for the ingredient book at CS places. Sometimes this will result in you having to wait for a manager to talk to you. Other times, they will just give you the book (this is one area where there seems to be no consistency). Because you may have to wait for a manager, try to get to CS places before your DD is really hungry (we learned this the hard way). We had a really long wait a couple of times and the kids were starving and miserable.

At TS places, the chef will come to your table and go over buffet or menu choices with you. Sometimes the bread on the table is safe, but most often, it's not. We've been to a few places where the chef made DD some allergy safe rolls since she couldn't have the regular dinner rolls. Also, some places have given her some crackers to munch on while the rest of us are having the bread. Baked goods (both breakfast items and desserts) are tough. Most of them will be off limits due to ingredients or cross contamination. However, Tusker House has Krispy Kreme donuts on their buffet and they're safe, so we always make an ADR there. There were a few places where the desserts were made in house and DD could have them, but at most places she ended up with ice cream.

We always bring hand wipes so that DD can clean her hands before she eats. Between railings, ride lap bars, door handles, etc. you have no idea what you are touching and what allergens might be lurking there, so making sure hands are clean before eating can minimize risk.

We also bring safe snacks to the parks, but we seldom need them. We always seem to be able to find something for DD. We've even done the Wishes Dessert Party twice and both times they were able to provide safe desserts for her.

Nut allergies can be really scary at first, but you'll be fine! We've been dealing with DD's for 10 years now and Disney is the easiest vacation spot when dealing with food allergies.

Have fun! :goodvibes
 
I don't advise ever going anywhere with only one Epi Pen. The Epi Pen only buys you time until paramedics can arrive, so if they take longer than 15 min to get to you, you may need another dose of epi. Also, what if one pen malfunctions or something else happens to one of the pens? Better safe than sorry and always have two.

I bring 6 Epi Pens for my DD when we travel. I'm sure it's overkill, but it's what makes me feel comfortable, so that's what I do. Once you decide on how many to bring, be sure to pack all of them (as well as Benadryl and any other meds your DD may need) in your carryon. Never put those meds in your checked luggage.

As others have mentioned, you need to ask for the ingredient book at CS places. Sometimes this will result in you having to wait for a manager to talk to you. Other times, they will just give you the book (this is one area where there seems to be no consistency). Because you may have to wait for a manager, try to get to CS places before your DD is really hungry (we learned this the hard way). We had a really long wait a couple of times and the kids were starving and miserable.

At TS places, the chef will come to your table and go over buffet or menu choices with you. Sometimes the bread on the table is safe, but most often, it's not. We've been to a few places where the chef made DD some allergy safe rolls since she couldn't have the regular dinner rolls. Also, some places have given her some crackers to munch on while the rest of us are having the bread. Baked goods (both breakfast items and desserts) are tough. Most of them will be off limits due to ingredients or cross contamination. However, Tusker House has Krispy Kreme donuts on their buffet and they're safe, so we always make an ADR there. There were a few places where the desserts were made in house and DD could have them, but at most places she ended up with ice cream.

We always bring hand wipes so that DD can clean her hands before she eats. Between railings, ride lap bars, door handles, etc. you have no idea what you are touching and what allergens might be lurking there, so making sure hands are clean before eating can minimize risk.

We also bring safe snacks to the parks, but we seldom need them. We always seem to be able to find something for DD. We've even done the Wishes Dessert Party twice and both times they were able to provide safe desserts for her.

Nut allergies can be really scary at first, but you'll be fine! We've been dealing with DD's for 10 years now and Disney is the easiest vacation spot when dealing with food allergies.

Have fun! :goodvibes

My daughter is crazy about the Tusker house donuts! I agree with you about the multiple epi pens--we'll see what the doc says next week, but I think over kill and what makes a parent comfortable is key. We are never without my med bag--even before this--always has benedryl, tylenol, etc, etc, etc. Basically a travelling drugstore.
Thanks
 
My daughter has a severe Tree nut/ Peanut allergy. You will find Disney World to be very accommodating. In day to day life my DD8 can not enjoy desserts etc when we dine out. She looks forward to our TS meals at Disney World. The Chef always makes her something extra special. I will never forget one of our meals at Ohanas. The chef brought her a brownie sundae like she had never been able to eat before. It was created on a shish kabob stick. Brownie/ice cream/brownie/ice cream/whip cream and cherries. Her eyes were as big as saucers !! She was soooo excited ! They made the Sundae using prepackaged peanut free brownies. I think you will be very pleased. just be prepared with your Epi Pens and benadryl along with lots of wipes. Hope you have a fantastic vacation.
 
Disney is the only place we go where my DD feels "no worries" about eating. They are AWESOME with food allergies. Unfortunately, she can't eat anything from the bakeries or the popcorn, which disappoints her, (tree nut/coconut allergy), but she still says she loves eating there. When you tell them you have a food allergy they don't look at you like you have 2 heads....they know exactly what you are talking about and how to handle them.
 
There is so much good information here, I just want to add when we took our recent trip to DW with our 2 yr old who has multiple allergies we were also very impressed by the attention we received at CS restaurants. The first place we went was Cosmic Rays for lunch and when I ordered a hot dog with no bun for my wheat allergic son the cashier asked me if he was allergic, when I said yes she immediately called over a manager who had a long conversation with me about my son's allergies and showed me the book of ingredients, including a selection of gluten free baked goods they offer as substitutions. My son couldn't have them because he also has milk and egg allergies, but it was nice to know the option is there. He then informed me that his meal would take a little longer because they would prepare his hotdog in a dedicated cooking area and would also fry his fries in a dedicated fryer to avoid any cross contamination. I nearly burst into tears right there, it meant so much to me to have his safety taken so seriously. I felt totally confident about the food I was giving him and it was a huge load off my mind. For me this is a big thing that makes Disney special.

At table service places our tickets always had ALLERGY stamped on them in red letters, they take it very seriously.

Good Luck

Chris
 
There is so much good information here, I just want to add when we took our recent trip to DW with our 2 yr old who has multiple allergies we were also very impressed by the attention we received at CS restaurants. The first place we went was Cosmic Rays for lunch and when I ordered a hot dog with no bun for my wheat allergic son the cashier asked me if he was allergic, when I said yes she immediately called over a manager who had a long conversation with me about my son's allergies and showed me the book of ingredients, including a selection of gluten free baked goods they offer as substitutions. My son couldn't have them because he also has milk and egg allergies, but it was nice to know the option is there. He then informed me that his meal would take a little longer because they would prepare his hotdog in a dedicated cooking area and would also fry his fries in a dedicated fryer to avoid any cross contamination. I nearly burst into tears right there, it meant so much to me to have his safety taken so seriously. I felt totally confident about the food I was giving him and it was a huge load off my mind. For me this is a big thing that makes Disney special.

At table service places our tickets always had ALLERGY stamped on them in red letters, they take it very seriously.

Good Luck

Chris

THis is great to hear. I'm working on a birthday cake for our trip in october for my 40th. Animal Kingdom blew me off, but I'm working on other options. It sounds great to hear how safe it is. We are going on a cruise in Sept and it's been harder. DD will celebrate her 3rd bday and they can't guarantee a nut free cake. I plan on talking to the chef when we board, but she may not get a cake this year. Anyone have any ideas for that one?
 














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