Showing posts with label Make a Wish. Show all posts
Showing posts with label Make a Wish. Show all posts

Thursday, December 22, 2011

Merry Christmas to Dear Son from Blendtec!





As many of you know, I’ve been a huge advocate of Now Foods Organic Virgin Coconut Oil for Dear Son. Once I started using it for Dear Son, I was able to nip any colds, flu or pneumonias from the start and since using it daily, Dear Son has not been hospitalized for pneumonia in 15 months. Prior to that, he had two to three a year. As you know, Dear Son has had a pretty rough time these past few years due to numerous hospitalizations. In 2009, the day before his Make a Wish trip, he came down with the swine flu along with a viral pneumonia and nearly died. At that time, the doctors told me that they did not think they could save Dear Son any more and that he would most likely die of pneumonia. He had several more hospitalizations after that and in May of last year, he was finally well enough to take his Make a Wish trip.


All total, it took six months from his hospitalization in 2009 for him to be able to sit up for two hours, long enough to make the trip to Disney in Florida. He still wasn’t well and we had to limit our activities. We had a wonderful time though. While we were there, we went to Universal Studios. One of my favorite memories from the trip was when we walked through the entry gates. They were enormous and it was like walking through the gates of heaven. As we walked through, I began to cry. We had spent months waiting to go on Dear Son’s Make a Wish Trip and we talked about it forever and when the swine flu happened, I thought we’d never make it. I felt like a failure in that I thought I waited too long to take the trip and thought he was going to die, having never made it. I had planned his Make a Wish Trip to coincide with his 18th birthday and instead, he got the swine flu the day before we left and he had respiratory failure the following day and was on a ventilator fighting for his life on his 18th birthday.






The Make a Wish trip was powerful for all of us. One of the things that it did for me and for us was to give us something to look forward to. When you care for a special needs child, it’s hard to do normal tasks of daily living so you don’t do as much as able bodied people because, well, everything is sooooo hard. But it wasn’t just that we had something to look forward to, the powerful part was that we broke the cycle of going to the hospital. For many years, the only placed we ever packed for was the hospital. Dear Son has been hospitalized some 70 plus times in 20 years and while most people have a packing list for their vacation, I had a packing list for the hospital.


After our trip, I vowed that I never wanted to go back to the hospital. I began researching things for us and discovered green spinach smoothies and organic, virgin coconut oil. I began drinking smoothies and was amazed at how I was able to relieve the pain from my arthritis with these amazing drinks. I started in June of 2010 and never looked back. Late last year, I discovered Now Foods Organic, Virgin Coconut Oil and began giving it to Dear Son. I soon learned how it would prevent colds, flu and pneumonia in him. It tooks months to figure out the right dose for Dear Son but I did and I am proud to say that it has now been 15 months since he’s been hospitalized with pneumonia. Certainly he’s had a few hospitalizations since then, but NONE have been for pneumonia.



A few months ago, I decided I wanted more for him. I thought that while the organic coconut oil was great once he had an illness, if I could build his immune system up, I could PREVENT sickness before it starts. I started reading about how I might use the nutrition in real foods and give that to him and take him off of formula feedings. (I had tried giving him real foods blended up but had failed since the food kept clogging the tube and I just gave up. )I made a list of all of my nutritional goals for him along with all of his conditions and began researching foods that would help each of his conditions. To give him real foods though would require a high powered commercial type blender, like a Blendtec or VitaMix. I researched the blenders and watched numerous videos and loved the Blendtec from the start. The Blendtec Total Blender would pulverize the food well, was easy to clean and fit under the cabinets and best of all, didn’t require a tamper. The only problem was that I couldn’t afford it. I mean these blenders sell for nearly $500 and I work part time so I can care for Dear Son who requires 24/7 care.

In early November, I sat Dear Son’s Dad down and told him I wanted a Blendtec for Christmas for Dear Son and I. I told him that I knew it was expensive, but that was the only thing I wanted for Dear Son. I normally never ask him for any Christmas gifts although he always gets Dear Son and I something nice. He hemmed and hawed a bit and I told him that I didn’t need an answer right away and that he should think about it. Then he said he didn’t think I’d make the food for him. But I persisted. He knew that I had been drinking green spinach smoothies for around 18 months and that I was into organic food and that it wasn’t a whim. He also knows I take really good care of Dear Son as does he. Then he asked what I’d do when Dear Son came to his house for the weekend. I said I would make all of Dear Son’s food and send it over. I sent him Blendtec videos and he still said no. Then I entered a Christmas Wish program on a local radio station asking for a Blendtec blender for Dear Son. It was the only thing I asked for.



Shortly before Thanksgiving, Dad asked for Christmas ideas for Dear Son. I told him that the only thing I wanted for Christmas was a Blendtec. I said I’d send him a list of some other options and sent him a list with the Blendtec at the top of the list. Here is what I wrote:



Blendtec Blender-"This is the only thing I want for Dear Son and I. I know
it’s expensive, but I can make his food and build his immunity to keep him well.
I’d rather have gift cards for the blender than anything else."


Right before Thanksgiving, I went to the Blendtec demo at our local Costco. They were offering the Blendtec and two blending jars for $474.99. I saw the demo and was excited. I called Dear Son’s Dad on the way home and told him about the demo. I tried the smoothies there and could taste the difference in the smoothness. I needed the blender to pulverize the food enough to get it through Dear Son’s feeding tube. The only thing I wasn’t clear on was whether or not there was BPA in the blender jars. So I sent Blendtec’s Customer Service an email regarding that issue.

Around this time, Dad called me and said he’d get the blender for us for Christmas. Blendtec responded to my email and clarified that the jars did not contain BPA and that they switched to BPA free jars in 2009. I thanked the customer service person and told her a little about Dear Son and how excited I was to get a Blendtec and start making his food to build up his immune system. And that was that.



Some two weeks later, I got an email from Blendtec. The person I wrote to had forwarded my email to their executives and they wanted to talk to me. They asked me for my phone number and the best time to call. A few hours later, I received a call from the customer service person. She said that she had forwarded my email to the executives at Blendtec and they wanted to send me a Blendtec blender! Can you believe that? I couldn’t! How cool is that? I mean, they had no idea how much I wanted a Blendtec and that it was the only thing I asked for at Christmas. They didn’t know how much I had been through with Dear Son or anything like that and yet, they offered to send me a reconditioned Blendtec blender. It was so exciting!



So let me show you my new baby….what do you think?






In this next photo, I am making tomato soup. It was delicious! Both Dear Son and I had some. I put his in through his gtube!







In this next photo, is Dear Son's first entire blended meal. I gave it to him today. This is a full day's meal although I am only giving him one blended meal a day for the first month as I need to transition him from formula feeds to blended foods gradually. More about that later. I created this entire day's meal. It includes: organic banana, organic strawberries, orange, organic spinach, organic broccoli, organic carrots, home made bread, organic chicken breasts, organic onion, walnuts (for omega 3's) and organic milk. It felt so good to give him this rather than formula. There was so much joy in making this for him! I got to be a real Mom again and make my son a "real" meal. Let me tell you, there was a lot of love in my kitchen today as I made up his food!





In this next photo, is the first smoothie I made in my new Blendtec!





So, all in all, a very exciting gift. It was so unexpected! Sometimes, Christmas wishes do come true!



Since I received the blender, I've been using it every day. I'll write more posts later on how to make a blended diet. In the meantime, Dad returned the Blendtec he purchased for me and instead, he'll give us the money to purchase some other items we need. And of course, I wrote Blendtec a lovely thank you note regarding our new blender.



What a wonderful way to end 2011. I just love this blender and it's amazing all of the things you can make. Everything I have made is just delicious. Thank you Blendtec for a wonderful gift and amazing product!



Note: If you'd like more information or to read more reviews on the Blendtec Four Side Blender, you can check it out here at my Amazon Store.

Friday, June 18, 2010

Dear Son's Make a Wish Trip~Day 7~Last Day!

Saturday, May 22, 2010~Day 7~Leaving Orlando!
Last pic at the villa before leaving for the airport!
At last, our trip was almost over. We had a great week and by now, Dear Son was really beginning to enjoy everything. Checkout time was 11 a.m. and our plane wasn't leaving until after 3 p.m. so we had plenty of time to kill. We stopped by the Gingerbread House for one last breakfast. After that, we checked out and headed over to the lobby.
Dear Son is really enjoying himself here! He seems genuinely happy and it's great to see him smile!

More pics from the lobby...

Dream Mom and Dear Son. I can't believe he's really 18!
After a while, I fed Dear Son lunch in the lobby and then Dad and Dear Son headed over to the ice cream parlor for one final visit. Give Kids the World was great because they notified us earlier in the week that they called and set up someone at security for us at the airport. Griff from Vacation Mobility met us at the airport for the van drop off. What a great rental service for people with disabilities! Unfortunately, once we got to the airport, security was unaware of our escort however they made a few calls and within minutes they had a TSA there to escort us through security. I requested a visual inspection since I was worried about Dear Son's VNS being activated. Supposedly, according to the manufacturer, you are o.k. at the airport however they request that you stay some 10-15 feet away from the scanners. I opted for the visual for him. The airport was totally swamped so Dear Son's visual inspection took quite a while. They were extremely thorough and checked his back, socks, etc. It took around fifteen minutes. I could not believe the great service we got though at both airports. Each time, we were escorted right through security and never waited in any lines. That was really appreciated.
Dear Son at the airport.
Finally, we boarded the plane. As you may recall, Dear Son was pretty scared when the plane started moving around for takeoff however after I explained to him that "men" really like flying and that the pilot was going to step on the gas and go really fast, he loved it. For the return flight, he was really happy once we got on the plane and couldn't wait to take off! You can see him smiling with excitement now!
Here he is smiling as we prepare for take off!

On our way home!


One we arrived at the airport, we had to wait around forty minutes or so for United to get the aisle wheelchair for Dear Son. Another couple had to wait for one as well for their disabled child. United needs a better policy so they can deliver the aisle wheelchairs in a reasonable amount of time. Disabled people shouldn't have to wait until everyone has left the plane and the new staff arriving before getting them a wheelchair. When tickets are ordered, there should be a box on-line for you to check so that they can have the chair available. One of the flight attendants for the next flight recognized Dear Son from our trip to Orlando and decided to give him some "wings". She pinned the wings on his t-shirt. He seemed to enjoy it.From there, it was onto Windy City Limousines. They have executive busses that are handicapped accessible. We were the only passengers both times. The bus was only a week or so old.
Arriving home (O.K. I might have used the departure photo when we left, lol!) Overall, a really great trip. We couldn't have picked a better place for Dear Son's trip. When I asked for suggestions, most of you suggested Give Kids the World at Disney and you were right on the mark. It was so easy for us. Everything was totally accessible. Give Kids went out of their way to do everything they could to make it easy. They set up the TSA at the airport. At Disney, everything we did was accessible and easy. The passes allowed us to go on rides without any wait times. This was especially great for Dear Son since he didn't have a lot of energy and often was exhausted after a few hours. Our wheelchair van was like icing on the cake. It took our trip to a whole different level in terms of making it easier. It wasn't just easy getting around but having the van meant we could leave when it was best for Dear Son and come home when he needed to leave. I know it was certainly Dad's favorite thing since he didn't have to do any lifting. Dear Son is getting to be a pretty big guy at 180 pounds to lift into the car.
After arriving home, Dad made a picture CD and movies for school so Dear Son could show his classmates his trip. His teacher had stated that everyone was so excited to hear about it since a lot of times, not much happens in these kids lives and this time, it was not only big news but good news. The kids loved the movies and one of his classmates was laughing the whole afternoon. They said it was the perfect end of school day.
Now that we've been home a while, we still spend time talking about the trip. Dear Son loves to talk about it and see pictures from the trip. He watches the Barney Show that Dad taped from our trip, on his t.v. He seems to almost enjoy the trip as much now as he did when we took it. It's just a little easier for him now to take everything in because he can enjoy it lying down in his bed or sitting in his chair.
His favorite thing from his trip seems to be the Mickey Mouse they gave him. Each day, GKTW left presents in the room for the kids. The first day was a Mickey Mouse and a large shopping bag full of presents. He continued to get presents every day and there were so many by the end of the week, that we couldn't take them all home. I took the ones that were age appropriate and that I thought he would enjoy and left the toys for able bodied kids there. He smiles every time he sees Mickey Mouse and he sleeps with him every night. Ever since the H1N1 last November, he seems to like these stuffed animals. They seem to provide a sense of security for him. I've never seen him like that before so it's definitely different. As for the Barney pillow, I put that between his ankles to support his legs/feet at night to prevent bedsores. In the last month, the addition of the pillow seems to have helped the swelling in his leg go down.

In the end, we had a great trip and a lot of great memories. Next month, when he goes to summer school, I make a scrapbook of the trip. In the meantime, it helps to pass the time thinking about the good times. Give Kids the World has a policy where any time you are in the area, you can come and spend the day there (providing you have other accomodations). I told Dear Son we might go back next year to visit and he just smiles. It's nice having something to look forward to.

In hindsight, I think this trip would have been more enjoyable for him two years ago, when he could do more and wasn't so exhausted. I say that because if you have a child and have the opportunity to take a trip like this, you should do it while they are well enough to enjoy it. I mentioned this to a friend of mine and she thought that it was the perfect time for Dear Son since this is when he seemed to need it most. After thinking about it some more, I think she is exactly right. Sometimes, we need all need a vacation just to get away and think about something different. In Dear Son's case, I think our timing was perfect. He seems so much happier now and although he's still tired, I can always get a smile by showing him Mickey Mouse, showing him pictures or just plain talking about our trip. And after everything he's been through, I am thrilled he has some great memories.

Thursday, June 10, 2010

Dear Son's Make a Wish Trip-Day 6-Epcot

Friday, May 21, 2010~Day 6
We decided to start the day with more character photos. Barney was scheduled to be here this morning and Dear Son was very excited to see him again. By now, Dear Son was starting to enjoy the vacation and had a better idea of what was going to happen. Sometimes, it takes kids like this a few times to see something before you can tell they are really enjoying it. After Dear Son's breakfast, we walked over to the Castle of Miracles to see him. Every Friday, they have different characters visit.
We were greeted instead by Scooby Doo! Apparently, Barney was there last week so it must have been a typo. Anyway, it was fun nonetheless. I don't think Dear Son really knows who Scooby Doo is though whereas he definitely knew Mickey and Minnie Mouse along with Goofy. One of his favorite movies when he was younger was, "A Very Goofy Movie". They used to watch it at school and said he would laugh like crazy when he watched it.
More photos...

It was great getting the character photos done here, at Give Kids the World, since it was easier for kids like Dear Son than standing out at Disney and waiting in line. It was great everything was so easy.

After the character photos, we headed over to the Gingerbread House for breakfast. This was the first time all week we came as a family. Dear Son eats via a feeding tube so it doesn't feel right to take him to a restaurant and let him watch everyone else eat so we usually just fed him at home and then came separately to breakfast and dinner.

More photos of Dear Son at the Gingerbread House. This place is packed for breakfast!

After breakfast, we headed over to Epcot. It was hard to believe the week was almost over. It went really fast.
I thought the flowers were spectacular here.
It was a beautiful day however it was still very, very hot. One of the things I wanted from this trip was family photos. I am not photogenic and never would take any family photos. When Dear Son's condition deteriorated, I realized that I didn't have any photos of our family or of Dear Son and I. I always took tons of photos of him. I tried to take some family photos so I could look back and remember how he looked. I realized that one day he will be gone and I wouldn't have any photos of our family. I won't get a second chance so I decided to not worry so much and just take the photos.
Hopefully, I won't bore you with the flowers. I just love them.


Dad and Dear Son...

The first thing we wanted to do was to go on the ride, "Soarin'". This was one of your suggestions; I remember someone said it was the, "best ride, ever!" We were really looking forward to it. This was a big attraction and there was a forty minute wait.

Give Kids the World gave us these passes so that we wouldn't have to wait in line. We showed the pass and they whisked us up through the disabled entrance and to these special lines for wheelchair access. We probably didn't wait more than five minutes in line.

They asked that we transfer Dear Son to the seats. Dad transferred him and then they took Dear Son's wheelchair. What's great is that they had the entire procedure down for people with disabilities. They offered to help Dad get him in the seat. Once Dear Son was seated, they told us he could ride two or three times if he liked, just let them know once we were done with the ride and they wouldn't make him get off the ride. Here's Dear Son checking everything out.

All ready to go!
They took the wheelchairs over to the center of the aisle. They kept them near the ride and told us they would bring them to us when the ride was over. They had plenty of people working there and it seemed like they were each assigned to help certain disabled patrons or whoever needed help.
The ride was a lot of fun! It took us over many scenic routes! All virtual reality of course, but really fun. Here's one of the scenes. I took a picture while we were on the ride so you could see. It was too dark for some of the other pictures to come out plus it was really fast.

After the ride was over, we rode again and then they brought the wheelchair over to Dear Son and offered to help us get him back into the chair. They couldn't have been more helpful.
Next, we decided to check out this ride called, "The Seas with Nemo and Friends".
It was a wheelchair accessible ride and the wheelchair pulled up right into the clamobile. It was nice to have a few things indoors where there was air conditioning. With Dear Son's patch, we had to make sure he didn't overheat so this worked out great.

Once inside, we took to the "seas". It was very pretty and almost as colorful as the movie.





Next, we stopped to give Dear Son his lunch.

After that, we took a little boat ride. They had an exhibit called, "Living with the Land" or something to that effect. EPCOT, is actually the acronym for, "Experimental Prototype Community of Tomorrow". EPCOT was originally designed to be a futuristic model with a community based on a type of utopian communal living. Once you get that, the rest makes some sense. The ride takes you through different ecosystems around the world. The idea is that our natural resources will be depleted over time and that we need to begin looking at alternative farming methods; all of this is branded under the name of "sustainability". Essentially, they show you futuristic methods such as soiless agrilculture where instead of using soil, they use just water and nutrients to grow plants (they state that the soil is unnecessary since it's just a reservoir for nutrients), of course it's artificial nutrients. They also showcase other ideas such as vertical farming where plants are stacked on top of each other in these planters creating an efficient method of watering. (See below photo for vertical farming.)
What I didn't like about the exhibit was that there wasn't any mention of genetic modification. Of course, these plants are genetically modified to produce higher yields and to be grown without soil, etc. I don't care for genetically modified foods and will avoid them as much as possible. I also want to know when an item is genetically modified. To go through this exhibit and listen to the entire tour without any mention of genetically modified fruits, vegetables or plants didn't seem right, although I was certainly not surprised.

Papayas...

Fluted pumpkins...

Cotton...
Bell peppers...

I should mention that Epcot also has a fireworks show every evening, complete with fireworks, lasers and music however Dear Son wouldn't be able to handle that. He goes to sleep at dinner time and doesn't get up until the next day.
All in all, a really great day. We did a few other things and then after Epcot, we decided to head home, rest a bit and then headed back to the pool. It was hard to believe we would be going home tomorrow! We wanted to make sure to enjoy that pool once last time. Have I told you how much we enjoyed the pool, lol!

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