Guest guest Posted April 11, 2004 Report Share Posted April 11, 2004 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, > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 14, 2010 Report Share Posted February 14, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 15, 2010 Report Share Posted February 15, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 15, 2010 Report Share Posted November 15, 2010 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. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 16, 2010 Report Share Posted November 16, 2010 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. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 16, 2010 Report Share Posted November 16, 2010 It could be the stress is less when you are away visiting than at home and that's what is affecting your arthritis more than the environment. Celeste Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 17, 2010 Report Share Posted November 17, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 23, 2010 Report Share Posted November 23, 2010 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 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 24, 2010 Report Share Posted November 24, 2010 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, Quote Link to comment Share on other sites More sharing options...
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