krisnme

I don't know your answer, but I hope someone does as I am curious as well, Mom is going to start infusions soon and I hope she does not have to stop cruising. I have wondered if it could be done by ships medical staff.

I cannot do that type of lengthy flight so until hubby breaks down and cruises out of the US to Australia I cannot visit one of my Pipe Dreams:(

 

Joanie

Awww. so sad for you.:( hope you get your dream one day. And thanks for adding the carry-on point, they do weigh a lot. Mom's provider said lighter poc's with smaller batteries are not too far in the future, hope she can still travel when they are available.

I think you need to speak to your poc provider, your Doctor, and review your own plans for your trip. some questions to ask: how long is my flight? most airlines require you bring extra batteries in case of emergency or flight delays. do you plan on excursions? how long? will you at any time be somewhere that an electrical outlet will be unavailable? If you cannot safely go without your oxygen for an extended period of time, you should err on the side of caution and bring more battery power than you think you need. remember, once you are at sea, there is no way to get another battery.

I travel extensively with my DS with multiple disabilities, I think when a child has to deal with medical issues daily, any distraction, however stressful for the caregiver can be so important to the child. I have found that most of my fears never happen, but so many rewarding moments do. plan for every and any disaster, but then sit back and enjoy. I can't help you with your specific issues, but can only lend support as a Mom, you can do this!

Sorry to open that can of worms! I really am just soaking up all the good advice, and I am sure we will figure out what will work best when we get to it. we are used to traveling a lot by plane, train, car and more recently boat and DS has always been a wonderful traveler so I hope Annie will adjust quickly to our meandering ways! Our trainer also runs several types of behavior and sporting groups so there are always options to expand on Annies training. My DS actually loves to watch "fly-balling" and hopes eventually to train her for this. My hope is to cruise again as soon as we feel confident. We haven't used a H/c cabin yet but I think it is time. DS is not as mobile as he used to be and the extra space for Annie would be nice. If you all ever get all together for a cruise, let us know!

You are so welcome. If I may be of some help. Don't forget to buy extra water and food dishes for the car and something collapsible for your purse.

 

We happen to live in an "earthquake" area so we keep an emergency supply of: water, leash, bowls, rain gear and food in the car. And, I have a "Brenda Bag" that I walk around with. I keep the collapsible water holder, extra food, emergency meds. in that bag. Brenda is very prone to ear infections so, I keep cotton swabs and her medicine in this bag.

 

I have a hook by our front door, on this hook are: Her leash, collar and CCI Vest. I can't go out the front door without passing all that she needs to have on.

 

You will find your very own "comfort zone" with "Annie" and what you will need to keep you and her life in sinc.

 

If you have any good ideas or suggestions we love to hear them!

Thanks, Only had 1 earthquake here, a 2.5 right under where I live, scared me to death but you would laugh at it! The bag idea sounds great. Kris and I are going to the fabric store this weekend to get fleece to make several "tied" blankets for Annie. we travel between family daily and often have daytrips and disney/Florida trips (we take the auto-train). I thought the blankets would be a good way to make her comfortable in all the places we spend our days. I am used to carrying food and water for Kris, as he has nutrition issues so I will just add some things for Annie to the bag. I will post pics the moment we get them. Any suggestions are welcome as we are completely new at this!

Thanks everyone for the warm welcome. will update you all as we learn more about Annie and get closer to bringing her home. My head is swimming with all the things we need to get for her!

Hi everyone!, let me start by saying how much I enjoy reading this board and learning sooo much! I am Mom to a 19yo son with multiple disabilities. we have been waiting and now are finally getting his SD in the next few weeks. She is a Golden and I am told is very blonde. My DS has named her "Annie". I suppose my first question for all of you is: How long should we wait after she joins our small family, to book our next cruise? I was hoping to cruise next year but will she need more time with us before we stress her with something like that?. I also have a question about how airport security handles screening dogs. I read a lot of blogs but don't really know how that works. we fly often and that will surely be our first big test. Thanks!

Oh hell yeah, I just LOVE those stares and giggles, I find if I go up to them and confront them they are the ones who end up cringing. I have quite a good line of put downs so pick on me and you pick on the wrong person :D And yes I do go up to them, if they are rude enough to comment or stare then I'm rude enough to go right after them. I always win :D I'm a confident beeatch like that :D

Wow, remind me not to look too much when you walk by! I am not a small girl by any stretch of the imagination, but if you are so quick to put others down, doesn't that make you just as bad?. My disabled son gets his share of stares, but once he smiles sweetly most people do the same, the others don't deserve my attention. I am really not trying to flame here, but that kind of nastyness may be why you get so many stares. I will remind my Autisic Son not to look too hard at large people (he is very curious) as they may "have a good line of put downs" and his innocence and curiosity may be misconstrued as rudeness.