Showing posts with label vacation. Show all posts
Showing posts with label vacation. Show all posts

Monday, September 17, 2012

Mexico in Shannon's Words (Part 2)

Shannon: 
January 5, 2011

At the airport

I thoroughly enjoyed my time in Mexico and successfully achieved my goal of getting absolutely not one bit more of color than I came with. The day before we left it was a snow blizzard in Maryland. We got to enjoy a bit of the winter white and then it was off to the airport to make our way down south and to the warmth of Mexico. We were supposed to leave at 10:30am and ended up flying sometime around 2:00pm. Not too bad all things considered.

It was the first time that I have flown since having my ancillary lymph node dissection. I followed precautions and put on my compression sleeve and gauntlet about an hour and a half before the flight. When I arrived in Mexico I noticed that my fingers looked very swollen. I was worried that the flying had caused me to get some swelling. However, the entire flight and after it I felt like the gauntlet piece was very uncomfortable. After about 45 minutes after landing I decided to take off just the gauntlet. After about 10 minutes I noticed that the swelling in my fingers was gone. When we arrived at the hotel 2 hours later I took off the compression sleeve and did not notice any swelling in my arm or hand.


Our trip was so nice and relaxing. I had just finished my sixth cycle of treatment and needed a nice relaxing time with my husband to just breathe, have some adventure, and enjoy life.

The first couple of days we were there we really just ate, read, sat on the beach, and went for walks together. We enjoyed this time very much. We especially enjoyed the second day when the sun came out nice and bright and all the iguanas came out of hiding to sun themselves.


Unlike the iguanas, I am not allowed to bask in the sun unfettered and unprotected. I took extra precautions to protect myself from the sun. I coated myself with Fallen’s COTZ sunblock. This is a very nice product. I only use it on my face because I can’t use regular or even standard sensitive skin sunblock on my face. This is the only thing that doesn’t irritate my eyes. I end up using very little so it is worth the price. For the rest of me I used a 70 spf waterproof sunblock. I also re-applied my sunblock not only according to the directions on the bottle, but also every time I swam and then dried off. I also wore a hat and sat under umbrellas at the pool or beach and also wore a coverup.


On the day we went to Chichen-Itza I decided that I did not need my compression sleeve and gauntlet. We did a whole lot of walking! I loaded up on the sunblock like our days on the beach and also wore a hat. During some of the tour guide’s talks the group was standing directly in the sun. I chose to forgo part of these learning experiences and stand in the shade on my own. It was incredibly fascinating and I was able to hear enough during the talks in the shady parts of the area that I did not feel my experience was in any way incomplete.

On Christmas Eve day we went to swim with the dolphins. I did wear my compression sleeve, but not my gauntlet because of it bothering my hand so much when I was flying. Now, salt and oil breaks down the special weave of fibers that the compression garments are made of. What I did was ask the place where I get my compression garments from what to do while swimming in salt water. I wore my old compression sleeve and immediately cleaned it when I got back from swimming with the dolphins.



That night at dinner I ate some thing that I was allergic to. I broke out in hives all over both arms, neck, and legs. I chose not to see a medic because my airways were not in any way restricted and I was having no trouble breathing. I had brought Benadryl with me and chose to take that as recommended. The hives lasted long after our vacation had ended. They were pretty much gone about a week after they popped up.

Our last two days were spent in lazy enjoyment. Ben played golf, we went shopping in Playa Del Carmen, (where I found a Starbucks!), and I got a hot stone massage and pedi-cure at the hotel spa. Now, one of the precautions one should take to prevent lymphedema is to avoid massages on that area. I simply told the spa that I could not be massaged on my right arm, shoulder, and the surrounding area of my arm. It was not a problem and I got to enjoy the perfect relaxing day.


I suppose now it is back to reality and New Year’s resolutions. I don’t usually make any, but I think I am going to this year…even if they will start a month late.

Last picture we took together in Mexico

Tuesday, August 14, 2012

Strength in Weakness, Part 3

Susan:

I can’t tell you the exact moment, the exact day, but I can tell you that when Shannon told me she and Ben were going to fly to Mexico for her first Christmas with cancer in December of 2009, I was shocked and upset. It was one of those moments, as her mom, that I did not hide how I felt. I told her to please reconsider, to go just one week later, to let us go with them-- I offered many alternative suggestions. But anyone that knows Shannon knows that once that little girl had her mind made up it was as good as done. She did offer to let us go with them but the more I thought about it and got the idea of what she was going for, I backed off. I did wonder how I was going to get through Christmas without her. She was really such a big part of our little family and the only other female beside me.



So Shannon and Ben were booked on a flight to leave BWI on Sunday December 20th. To fly, Shannon had to make several different accommodations for herself. She had to bring medicine that had to be refrigerated. She had to make special arrangements with the airline to transport the medicine. Shannon had to fly with a compression sleep and glove and this would be her first time testing it out. I worried about many things.  If she swelled what would they do for her in Mexico? Also, if she got sick with any side effects what would they be able to do for her in Mexico? How would they be able to fly her back to the states if she had swelling due to the ancillary lymph node dissection?

I don’t know if Shannon gave much thought to any of that. She was not the worrier that I was, thankfully!

The first thing Shannon and Ben had to overcome was a huge snow storm. The storm began on Saturday night and continued on into Sunday the day they left. They got out of BWI right before they shut down the airport. Breathe Susan breathe! OK – on their way. I prayed hard that she had no reactions to the compression in the plane. 



Once Shannon and Ben arrived we could not call due to roaming charges and I wanted to let her find her way and get settled but she did email me to let me know they had arrived and she described the little room off the lobby where she could email and also Skype with me and her dad.

Shannon also let us know that she did not swell badly and by the time we spoke the swelling was going down. So far so good right?

During this week Shannon and Ben did many fun things. They spent time on the beach-- for Shannon this meant totally covered. They took an excursion to see ruins. They swam with dolphins and we have a picture of Shannon kissing one with her compression sleeve on. They had romantic dinners under the moonlight and tried different dishes. 



When Christmas day came I had arranged to do things differently to try to make up for her absence. Sean’s Dad, his brother Mark, Christopher, Sean and me all went to Carroll’s Creek for brunch. It was all very nice. Afterward, Christopher, Sean and me watched Sherlock Holmes with Robert Downey Jr. That night Christopher’s kids were flying in from Florida for their Christmas break weekly stay with their dad. So we had something to be excited about. But for me the highlight of that day was when we got on Skype with Shannon. I craved her female presence in our family gatherings. I did not love one of my children more than the other. But I had one very sick child in Mexico and she was my only daughter and I desperately craved her presence. After we used Skype and I laughed at her antics and funny stories I felt relaxed and ready to enjoy the rest of my family evening. Everything just felt right with the world.

Shannon probably had some type of internal bucket list or something like that. Because she was constantly reaching beyond what was expected of her. Doing for others in extraordinary ways and treating herself and her husband to an unusual but fun way to spend Christmas when you have recently been given a prognosis of 3-5 years to live. Looking back now I see so many things that she did that were daring and areas where she absolutely pushed herself beyond her physical limit.

Shannon was living her life to the fullest and enjoying each moment as if it could be her last. Her motto when she talked to me was always-- she was hoping for healing but if it was not to be so then she accepted that she might die. She was mature beyond her years and made me very proud by the example that she set.