Jump to content
RemedySpot.com

Re: Traveling Question

Rate this topic


Guest guest

Recommended Posts

Guest guest

Hey -

I don't think you should stress over it. You can do the weight workouts

when you're at home or have access to a gym - maybe bring some hand weights

with you when you're camping (keep them in the vehicle?). Use gallons of

water or cans of stuff to lift with. Or you can just do variations of

pushups and situps while you're travelling. I was in the Army for a while

and that's pretty much all we did were pushups, situps and run and

variations of all of those. Like wide pushups (arms wide apart-works

different chest muscles), diamond pushups (hands close together and arms

close to your sides -works more triceps/arms) - and regular situps, side

crunches - all sorts of ab-work on the floor.

Oohh - oohh - get a balance ball and bring it with (deflate it for each trip

if you must).

Just some suggestions - hope that helps!

in WI

Traveling Question

> Part of my hesitation in " officially " starting BFL is that we will

> be traveling quite a bit in the upcoming months. Our trips range in

> length from four to seven days, usually one a month, but two in May

> and continuing through October. We will be camping, so I imagine

> that I'll be able to get some cardio in with walks and hikes, but

> not anything strenuous since I have three little ones tagging

> along :) Does anyone have any suggestions for how to keep up with my

> strength training? If it was just one trip, I wouldn't really worry

> about it, but since it is going to be monthly, I wanted to have some

> ideas of how to continue my workouts.

>

> Thanks,

>

>

>

>

>

>

>

Link to comment
Share on other sites

  • 5 years later...

My daughter wore a mask and we went to guest services and got a pass to go to

the top of the lines!!!!

 

BYrd

   

 

http://www.caringbridge.org/visit/deanabyrd

        

________________________________________________________________________________\

___________________

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately?  I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice.  Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?).  The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can! 

-

Mom of 6-yr-old boy/girl twins with PID

________________________________

From: Barbara Jimenez <mother5590@...>

Sent: Sat, February 13, 2010 9:31:33 PM

Subject: Re: Sinus surgery questions

 

Hi, My daughter is now 19 and had the surgery when she was 7. She is NOT immune

deficient but her brother has CVID. Both of the kids had HORRIBLE sinus

infections. Requiring IV antibiotics for 6 weeks each on several occasions.

A veteran ENT at Seattle Childrens Hospital  told me that my daughter had the

worst sinus infection he had ever seen including the temperal sinuses. Which

from what he said they should not have been developed until the early 20's. I

did allow them to do the surgery you are talking about and then we did 6 weeks

of IV antibiotics and steroids.Within 6 months they had to go back in and she

has had 5 surgeries since that time.  AND Sadly now has no health insurance and

cannot get any and has a NASTY sinus infection again. So... I have to say I am

not sure if it helped. I also believe it changed the bones in her nose/face to

some degree. Nothing supermajor but she has a bump on her nose that was not

there before. I would look into this ahead of time if I had it to do again.

It may be very necessary to clear your daughter out again for her current

infection. I would really consider taking her to a major medical center ENT for

a second opinin along with an Immune overview. The only thing we have found that

does work is the ongoing  sinus daily rinses. We use the Grossan pulsating nasal

irrigator. It is MUCH better than the water pik in my opinion. It is designed by

an ENT.

I will have to say that because my kids are adopted and they both had these

serious infections we began to look for another cause. AND.... we found mold in

our attic that was getting into the furnace. (bad flashing on the roof) It was a

MAJOR nightmare and we are not sure whether that was the trigger for my son's

immune problems or not. ( he was a newborn). The EPA has a division in each

state that will check your house for free. Ours was called the Indoor Air

Pollution Authority. We were shocked when we found the mold since it was in the

garage attic and would never have found it on our own.

I know this is not good news but it atleast gives you one perspective. You may

have to get her cleared out good either way. Oh also we used pulmicort in the

nasal rinser and it helped much more than the nasal sprays since they gave my

son bloody noses. Feel free to contact me directly if you want to talk any

further.

BARBIE 

____________ _________ _________ __

From: beyeafamily <debeyeaverizon (DOT) net>

groups (DOT) com

Sent: Sat, February 13, 2010 12:33:50 PM

Subject: Sinus surgery questions

 

I know several of you deal with recurring sinus infections in your kiddos. I've

posted before about my 8 yr old daughter with the severe sinus issues.

We've been working with our ENT, who gave us a few options. Basically, even

though she is on IG replacement, has been on Augmentin for 5 weeks, doing nasal

sprays/rinses, etc. she still 'looks terrible' on her sinus endoscopy this past

Thursday. He says that her sinuses are completely occluded. On an MRI that she

had, it showed extensive damage to her sinus areas, that has progressed quite a

bit in this past year since her last MRI. One of the options he gave us was him

going in and doing a surgery that will open everything up (her largest problem

area is her temporal sinuses) drain everything, and put antibiotics right into

the affected areas.

The surgery would last about an hour and a half, and carries quite a bit of

risks, not to mention that's a long time for a mito kid to be kept under

anesthesia. Her last sinus surgery with anesthesia she had pneumonia/partially

collapsed lung following the surgery, so both us and ENT doc are concerned about

those risks.

I guess my question is has anyone had this done, and did it help? Did it give

only temporary relief or has it been a huge success? We really don't know what

to do. Obviously what we are doing has not been working, and it is really

affecting her quality of life. She has been having horrendous headaches which

leave her barely able to get through the day.

Also, has anyone found a reason besides the immune deficiency to explain severe

and extensive sinus damage despite being on Immune replacement?

thanks

a

mom to 4 wonderful girls, dealing with Mito, Eos, g-tubes, seizures, immune

deficiency, etc.

Link to comment
Share on other sites

My daughter wore a mask and we went to guest services and got a pass to go to

the top of the lines!!!!

 

BYrd

   

 

http://www.caringbridge.org/visit/deanabyrd

        

________________________________________________________________________________\

___________________

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately?  I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice.  Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?).  The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can! 

-

Mom of 6-yr-old boy/girl twins with PID

________________________________

From: Barbara Jimenez <mother5590@...>

Sent: Sat, February 13, 2010 9:31:33 PM

Subject: Re: Sinus surgery questions

 

Hi, My daughter is now 19 and had the surgery when she was 7. She is NOT immune

deficient but her brother has CVID. Both of the kids had HORRIBLE sinus

infections. Requiring IV antibiotics for 6 weeks each on several occasions.

A veteran ENT at Seattle Childrens Hospital  told me that my daughter had the

worst sinus infection he had ever seen including the temperal sinuses. Which

from what he said they should not have been developed until the early 20's. I

did allow them to do the surgery you are talking about and then we did 6 weeks

of IV antibiotics and steroids.Within 6 months they had to go back in and she

has had 5 surgeries since that time.  AND Sadly now has no health insurance and

cannot get any and has a NASTY sinus infection again. So... I have to say I am

not sure if it helped. I also believe it changed the bones in her nose/face to

some degree. Nothing supermajor but she has a bump on her nose that was not

there before. I would look into this ahead of time if I had it to do again.

It may be very necessary to clear your daughter out again for her current

infection. I would really consider taking her to a major medical center ENT for

a second opinin along with an Immune overview. The only thing we have found that

does work is the ongoing  sinus daily rinses. We use the Grossan pulsating nasal

irrigator. It is MUCH better than the water pik in my opinion. It is designed by

an ENT.

I will have to say that because my kids are adopted and they both had these

serious infections we began to look for another cause. AND.... we found mold in

our attic that was getting into the furnace. (bad flashing on the roof) It was a

MAJOR nightmare and we are not sure whether that was the trigger for my son's

immune problems or not. ( he was a newborn). The EPA has a division in each

state that will check your house for free. Ours was called the Indoor Air

Pollution Authority. We were shocked when we found the mold since it was in the

garage attic and would never have found it on our own.

I know this is not good news but it atleast gives you one perspective. You may

have to get her cleared out good either way. Oh also we used pulmicort in the

nasal rinser and it helped much more than the nasal sprays since they gave my

son bloody noses. Feel free to contact me directly if you want to talk any

further.

BARBIE 

____________ _________ _________ __

From: beyeafamily <debeyeaverizon (DOT) net>

groups (DOT) com

Sent: Sat, February 13, 2010 12:33:50 PM

Subject: Sinus surgery questions

 

I know several of you deal with recurring sinus infections in your kiddos. I've

posted before about my 8 yr old daughter with the severe sinus issues.

We've been working with our ENT, who gave us a few options. Basically, even

though she is on IG replacement, has been on Augmentin for 5 weeks, doing nasal

sprays/rinses, etc. she still 'looks terrible' on her sinus endoscopy this past

Thursday. He says that her sinuses are completely occluded. On an MRI that she

had, it showed extensive damage to her sinus areas, that has progressed quite a

bit in this past year since her last MRI. One of the options he gave us was him

going in and doing a surgery that will open everything up (her largest problem

area is her temporal sinuses) drain everything, and put antibiotics right into

the affected areas.

The surgery would last about an hour and a half, and carries quite a bit of

risks, not to mention that's a long time for a mito kid to be kept under

anesthesia. Her last sinus surgery with anesthesia she had pneumonia/partially

collapsed lung following the surgery, so both us and ENT doc are concerned about

those risks.

I guess my question is has anyone had this done, and did it help? Did it give

only temporary relief or has it been a huge success? We really don't know what

to do. Obviously what we are doing has not been working, and it is really

affecting her quality of life. She has been having horrendous headaches which

leave her barely able to get through the day.

Also, has anyone found a reason besides the immune deficiency to explain severe

and extensive sinus damage despite being on Immune replacement?

thanks

a

mom to 4 wonderful girls, dealing with Mito, Eos, g-tubes, seizures, immune

deficiency, etc.

Link to comment
Share on other sites

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have

problems with body temperature regulation then they will accomodate you to put

you in a controlled environment. This doesn't always mean front of the line but

waiting in a space that will allow them to be comfortable until their turn

comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.com discusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have

problems with body temperature regulation then they will accomodate you to put

you in a controlled environment. This doesn't always mean front of the line but

waiting in a space that will allow them to be comfortable until their turn

comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.com discusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbridge.org/visit/deanabyrd

________________________________________________________________________________\

___________________

________________________________

From: Ursula Holleman <uahollem@...>

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have

problems with body temperature regulation then they will accomodate you to put

you in a controlled environment. This doesn't always mean front of the line but

waiting in a space that will allow them to be comfortable until their turn

comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbridge.org/visit/deanabyrd

________________________________________________________________________________\

___________________

________________________________

From: Ursula Holleman <uahollem@...>

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have

problems with body temperature regulation then they will accomodate you to put

you in a controlled environment. This doesn't always mean front of the line but

waiting in a space that will allow them to be comfortable until their turn

comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

If she's that compromised have they talked about a transplant?

Ursula

On Feb 14, 2010, at 4:51 PM, " Mrs. Byrd " <kitkat32308@...> wrote:

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbridge.org/visit/deanabyrd

__________________________________________________________

________________________________

From: Ursula Holleman <uahollem@...>

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have problems

with body temperature regulation then they will accomodate you to put you in a

controlled environment. This doesn't always mean front of the line but waiting

in a space that will allow them to be comfortable until their turn comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

If she's that compromised have they talked about a transplant?

Ursula

On Feb 14, 2010, at 4:51 PM, " Mrs. Byrd " <kitkat32308@...> wrote:

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbridge.org/visit/deanabyrd

__________________________________________________________

________________________________

From: Ursula Holleman <uahollem@...>

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have problems

with body temperature regulation then they will accomodate you to put you in a

controlled environment. This doesn't always mean front of the line but waiting

in a space that will allow them to be comfortable until their turn comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

what kind of transplant?? No they have not.

BYrd

http://www.caringbridge.org/visit/deanabyrd

________________________________________________________________________________\

___________________

________________________________

From: Ursula Holleman <uahollem@...>

" " < >

Sent: Sun, February 14, 2010 5:32:51 PM

Subject: Re: Traveling Question

If she's that compromised have they talked about a transplant?

Ursula

On Feb 14, 2010, at 4:51 PM, " Mrs. Byrd " <kitkat32308@...> wrote:

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbridge.org/visit/deanabyrd

__________________________________________________________

________________________________

From: Ursula Holleman <uahollem@...>

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have problems

with body temperature regulation then they will accomodate you to put you in a

controlled environment. This doesn't always mean front of the line but waiting

in a space that will allow them to be comfortable until their turn comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

what kind of transplant?? No they have not.

BYrd

http://www.caringbridge.org/visit/deanabyrd

________________________________________________________________________________\

___________________

________________________________

From: Ursula Holleman <uahollem@...>

" " < >

Sent: Sun, February 14, 2010 5:32:51 PM

Subject: Re: Traveling Question

If she's that compromised have they talked about a transplant?

Ursula

On Feb 14, 2010, at 4:51 PM, " Mrs. Byrd " <kitkat32308@...> wrote:

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbridge.org/visit/deanabyrd

__________________________________________________________

________________________________

From: Ursula Holleman <uahollem@...>

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have problems

with body temperature regulation then they will accomodate you to put you in a

controlled environment. This doesn't always mean front of the line but waiting

in a space that will allow them to be comfortable until their turn comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscusses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: tracy ulvap <pavlutracy@...>

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

Bone marrow (or stem cell/cord blood) transplant.

Ursula

Mom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

________________________________

From: Mrs. Byrd <kitkat32308@...>

Sent: Sun, February 14, 2010 7:04:57 PM

Subject: Re: Traveling Question

what kind of transplant?? No they have not.

BYrd

http://www.caringbridge.org/visit/deanabyrd

____________ _________ _________ _________ _________ _________ _

____________ _________ _________ __

From: Ursula Holleman <uahollem (DOT) com>

" groups (DOT) com " <groups (DOT) com>

Sent: Sun, February 14, 2010 5:32:51 PM

Subject: Re: Traveling Question

If she's that compromised have they talked about a transplant?

Ursula

On Feb 14, 2010, at 4:51 PM, " Mrs. Byrd " <kitkat32308> wrote:

They moved her to the front of the line to limit her exposure to large crowds of

people as much as possible. Instead of waiting for 45 min around who knows what.

BYrd

http://www.caringbr idge.org/ visit/deanabyrd

____________ _________ _________ _________ _________ _________ _

____________ _________ _________ __

From: Ursula Holleman <uahollem (DOT) com>

groups (DOT) com

Sent: Sun, February 14, 2010 4:42:05 PM

Subject: Re: Traveling Question

We have season passes to disney and use their Disney Vacation club for the

condo. I'm not sure what type of problems your children have but accomodations

usually are done per problem not for a " disability " label. If they have problems

with body temperature regulation then they will accomodate you to put you in a

controlled environment. This doesn't always mean front of the line but waiting

in a space that will allow them to be comfortable until their turn comes.

If there are respiratory problems (O2 needed, wheelchair due to stamina) then

they will allow you this in the park and place you in the wheelchair line

waiting until the next accessible ride comes along. If your child can transfer

from a wheelchair to a ride seat then your turn will come about the time it

would have in a regular line.

This forum on disboards.comdiscus ses accommodations

http://www.disboards.com/forumdisplay.php?s=b8bb6b3c52d9530d392b404ccb416c4c & f=2\

0

You'll want to go to Guest services when you get to the park and ask for a GAC

(Guest Assistance Card)

http://www.diz-abled.com/Disney-Resources/Articles/Disney-Guest-Assistance-Cards\

..htm

another good link for info.

We go about twice a year and Macey usually uses her transport chair.

UrsulaMom to (17) and Macey (14)

http://www.caringbridge.org/visit/maceyholleman

____________ _________ _________ __

From: tracy ulvap <pavlutracy (DOT) com>

groups (DOT) com

Sent: Sat, February 13, 2010 11:45:59 PM

Subject: Traveling Question

Has anyone traveled to Disney World w/ their PID kids lately? I'm not sure DW

will be able to provide us with any helpful/special accommodations, but thought

I'd see if anyone had any advice. Since the kids do not have a " typical "

disability (you can't tell by looking at them), it is probably not reasonable to

expect any modified treatment from DW--not even sure what accommodations they

could make that would make a difference (think they could put us in a bubble &

float us around?). The kids are looking so forward to the trip & I want to

provide the best situation for them as I possible can!

-

Mom of 6-yr-old boy/girl twins with PID

Link to comment
Share on other sites

  • 8 months later...

When I travel, I often have the same experience, although mine has usually

involved travel to warmer/dryer climates, since I live in the Pacific Northwest.

If you want to move to be near family, I would recommend it, but am not sure if

it is our weather here. I live on an island in the " rain shadow " (so only 12

inches rain/yr compared to Seattle's 30), yet I still hurt frequently. However,

I do notice more pain during our rainy spells.

Dena

Link to comment
Share on other sites

I would first look to stress in your home environment. This could include not

being happy with one's mate, loneliness, the actual space - itself, a job or

boss that you dislike...etc. After that, I would look at environmental causes

related to allergies - food, air borne, soaps, mold etc.

Link to comment
Share on other sites

I definitely have more pain during we weather!  By the way, I love your name.  I

had a beloved Aunt Dena, who was like a mother to me.  She passed away suddenly

two years ago with a brain aneurysm. Don't hear the name very often!

Take care.

Link to comment
Share on other sites

When I travel... my body doesn't hurt half as bad as it does when I am at home.

I really think it is because you are so much more relaxed and everything just

feels better!

Best of luck,

Kassandra

Link to comment
Share on other sites

I also live in New England (NW of Boston) and I always feel better when I get

out of the region. I travel frequently to Florida, and my body loves the clean

air, warm sun, and humidity that Florida is known for.

I think part of it is definitely physical - I feel better in the summer and

worse in the winter - but I also think that it is part psychological. I agree

with the idea that it could be that you were more relaxed and experiencing less

stress when on vacation, and it's indisputable that stress makes us feel worse.

I haven't been to the southwest since I was diagnosed, but I would be willing to

bet that the climate definitely had a positive effect on your health and

well-being. There is a reason that the majority of people on this planet are

living close to the equator and that people in cold climates have more physical

ailments, vitamin deficiencies, and other health issues.

I am moving to a warm climate as soon as I am able!

Doreen

Link to comment
Share on other sites

Hi Doreen and all,

I too live just north of Boston! I think the stress and relaxation factor is

the key.

I am fortunate that I love to travel and do often. I am mostly symptom free due

to my weekly MTX. But I know when I get stressed I often start to have a creaky

joint here or there I have been to desert climates, rain forests, hot, cold,

frigid, you name it. I generally do not experience symptoms when away, but

sometimes while actually traveling, the stress of making a connection or missed

flights can help trigger an ache or more often a skin eruption of P.

I do know that getting sun and sun exposure does help me. Luckily I am an avid

sun worshiper and have easy to tan olive skin.

Stay well,

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...