Wednesday, April 21, 2010
EULOGY FOR SHANNON WATSON - BY HER LOVING HUSBAND
Thursday, March 25, 2010
Since Arizona
Wednesday, March 3, 2010
I'm in Arizona
Wednesday, February 17, 2010
Winter Blues and my great idea
I am just plain sick of this weather. I cannot believe it has not gotten over 30 degrees in weeks and weeks. The sun is non-existent here and the 10 day forecast never shows me any sign of relief. Usually I love winter but that is because I LOVE snowboarding. Since I cannot walk up the stairs without feeling like I could faint, there is no way in hell I could suit up and get out on the mountain and make it down the hill. Snowboarding was the highlight of my winters, but now I have nothing to look forward to. It’s only mid February and time is going slow since I am sick in my house.
My health has been struggling. I’ve been really sick and tired. Weak, sore, the list goes on and on. I’ve had to have people, like my friend Todd, take care of me every day since it is so hard for me to move around. I’ve had to have another blood transfusion. Pretty soon I will have a scan and we will hopefully see if this chemo is even working. The Penguin Caps may not be working anymore with this new chemo I am on called Abraxane. This past Friday I started having hair fall out. Every day it got worse and worse. I got one more round of chemo hoping that it wouldn't be the end of my hair, but it didn't work out that way. Today my hair was coming out 100 strands at a time. I was making a mess all over the house. Kevin shaved my head and I am now once again, for the third time in my life bald. The Caps worked for Gemzar, Cisplatin, and Carboplatin, but Abraxane is too strong for them. It's supposed to be easier on your body and bone marrow which is good since I was having to have so many transfusions, but it's really hard on hair loss. Oh well. Here is my list of positives now that I am bald...
1. Chemo will be super short. Maybe an hour and a half tops.
2. No more hair falling all over the house
3. I don't have to freeze my head anymore
4. I don't have to pay for the cold caps
5. I found a couple cute new wigs I should be getting within the next week
6. I get to hear everyone tell me how I can pull off the bald look
7. I don't have to be extra careful not to make my hair fall out when I shower
8. No more shampoo (since I am really smell sensitive and I end up hating every shampoo smell within a week of using a new one)
9. No more stressing about if all my hair will fall out or if it is just thinning. The mourning process is pretty draining on the spirit.
Anyway, I am convinced the caps work for some chemos, but not all. Not Abraxane.
I'll get some bald pics and show you all as well as new wig pics once I get them.
Trying my hardest to be positive
Shannon
Saturday, January 23, 2010
Thursday, January 21, 2010
The Rest of the Photo Shoot Pictures with Melissa
And of course I had Uncle David's commentary the entire time making me laugh so it was easy to have a natural smile.
A more serious one.
I did have a few of those fake eyelashes on so that is why my eyes look a lot better. My eyelashes are very short normally.
Laughing at uncle david again.
Melissa normally works with models. In some of her past photo sessions they have painted words on the models faces for the pictures. I was able to pick out the words I wanted written on my face. Hope, Love, Passion, Truth, Peace, Strength and a Chloe paw print is what I picked. I do have a tube top on and I have the blanket wrapped around me as well. The picture is cropped exactly where the shirt and blanket end.
After we did a number of these pictures we painted my lips white too.
And that is the rest of the pictures from the photo shoot. It was a lot of fun. I was surprised how good I looked despite having a really bad fever. The makeup worked really well for covering up black circles under the eyes.
Monday, January 18, 2010
Photo Shoot With Mellissa and Uncle David
Monday, January 11, 2010
Going to California
The first day I pretty much just chilled around their house. I opened every window in the sunroom, layed in the sun on the huge comfy bean bag and smelled the freshly cut grass as the lawn crew did all there work. There was a perfect Breeze to cool me off when I needed and it would also bring the grass smell rushing back in the room. After the
yard crew was done I got in little shorts and a tank top, grabbed a
lawn chair, a book and some shades relaxed and worked on my tan. Some
would say I did nothing that day, but for me it was awesome. Plus I got
to hang out with a really cool, smart, carrot loving dog of my uncle's, Ranger.
I might have overdid it in the sun because my skin was burning up all
night and I was completely drained, but oh well. I usually feel like
that all the time anyways, so what's the difference.
Day 2 I woke up with a mission. I was going to the beach. Now, it
might seem like everything is a-ok with my body, but nothing could be
further from the truth. When I left I was dealing with horrible bone
pain and 103.3 fever. Well, the infection picked up and my throat is
pretty raw. I still have fevers but lower grade. My bone pain was
replaced with some muscle pain that was very intense. I think my
muscle might be pinching a nerve. Then, the bone pain also came back.
On top of all that I have a headache that will not go away. I am so
sick of taking pain medicine, but I can't function without it the pain
is so bad. Moral of the story is, I can change my environment and love
it, but I can't change what is going on with my body.
Honestly though, just changing my environment is proving so refreshing
to me. Not being in my bedroom where I sweat all the time and have
sleepless nights. Not being on my couch where I resort to when I have
no more chance of going back to sleep. Not looking outside at the same
yard covered in snow and seeing the usually grey skies. Out here
everything is alive. There are flowers in bloom. It smells different.
I'm in a different bed without any negative stigma that I created like I have with my bed at home.
The beach was great. I went to Malibu first and watched the surfers.
There were some big waves. Then I drove down to the Santa Monica Pier
to have lunch. Afterwards I sat on the beach again. It was so nice and
relaxing. I love the smell of the ocean. My sense of smell has been
like a dogs since I started chemo. I can smell things from so far away
and everything smells so strong. Bad thing is, most of the smells make
me feel sick. All colognes and perfumes, anything scented, laundry
detergent etc etc.... But this day I could smell the ocean from inside
the resturant I was in and it was wonderful. I wish I could trap that
smell and somehow tape it over my nose.
My uncle's girlfriend Melissa and I watched Julie and Julia at night
and ordered Chinese. It was very nice and relaxing.
Today is day 3 and I have the worst bone pain ever. I was stuck in my seat and couldn't move because it hurt me so bad. I had the same thing a couple days before I left for California. I have to take Oxycodone and Oxycotin together. Those two combined make me pretty sick. I was throwing up a lot. I can't handle those two medicines combined. Actually I threw up here in California on just the 4-6 hour Oxy, so I just cannot tolerate that stuff. Anyway, just because I was in pain didn't stop me from getting a lawn chair and sitting out in the sun until I finished my book. I'm getting by though. I'll let you know how the rest of the trip goes. I am very happy I came out here. Still having a great time despite what is going on with my body.
Sending sun and warmth to everyone
Shannon