Sunday morning we had an early morning hockey practice at Erin Woods. After the practice the entire team decided to go out for breakfast. It was nice to go out with everyone and enjoy a nice breakfast with the team. The kids both had a good time with all the players. After breakfast we went swimming at the Southland Leisure Centre. It had been a long time since she had been allowed to go out to somewhere like a pool. She had a great time playing in the waves and going down the slides.
Sunday afternoon Ryley and Dad headed to the Heritage Classic. For anyone who doesn’t know the Heritage Classic was the outdoor hockey game between the Calgary Flames and the Montreal Canadians in front of 41,000 people at McMahon Stadium. We had special seats through Hockey Calgary with a limited view on the ice. We were in row 4 which was too low to be able to see most of the ice surface. The opening ceremonies with incredible; Paul Brandt sang the national anthem, the Snowbirds did a flyover and there were lots of fireworks and flames. The game was very cold and the crowds in the concourse were insane. You could not move and everyone was pushing and shoving. The lines for the washroom and food were incredibly long and slow. We made it through one and a half periods and then decided that we should go home and get warm. Overall it was a great experience and Ryley enjoyed the atmosphere and the fun; best of all the Flames played a great game, Kipper got a shutout and Montreal lost!
Monday was family day in Alberta and another outdoor game. We got better tickets to the WHL Outdoor Game. It was a lot warmer and the game started much earlier so it was warmer. The seats were on a very cold metal bench, but we had lots of warm stuff to sit on so it wasn’t too bad. We got to see a friend’s son do the pregame skate with the Hitmen and then enjoyed a couple of periods of hockey. Once again everyone started to get cold so we all headed home.
Karlee went to preschool both Tuesday and Wednesday and is starting to fall into a routine. She was at the front door on Tuesday dressed and ready to leave 30 minutes early. She is having a great time doing crafts and learning music. Hopefully we don’t have too many clinic days that interfere with her preschool days.
Thursday was clinic day and this time it was Dad’s turn to head up. Clinic day was really smooth and we left the hospital around 1pm. Mom didn’t tell Dad how much fun clinic day is now. The nurses were all having a great time joking around, we played a little DS, did a craft and watched some TV. Karlee and Dad both had fun and we got all the drugs and fluid into her without issue. Once again today reminded me of how lucky we are. There was a little girl just younger than Karlee. It took about 10 minutes of her yelling and screaming just to get her accessed. Karlee just sits there and talks to the nurses while they access her.
Thursday night we went to the final Skate-A-Thon meeting. We went through all the prizes for the bucket draws and got a few things finalized. We are going to have some great prizes packages. Now we need to makes sure we get lots of people out to support the event. If you have any questions about the Skate-A-Thon let me know at ronlewis@telusplanet.net.
Thursday, February 24, 2011
Saturday, February 19, 2011
Clinic Day & Preschool
Mom and Karlee headed up to the hospital at 7:30 Monday morning assuming that it would be a standard Monday morning for traffic. They were at the clinic before 8:15 – 45 minutes early for their appointment. Fortunately they took them in early and got her accessed and ready to go. Her counts came back great so she was good to go today. She had a procedure to inject chemo into her spinal fluid and then she received 2 different chemo drugs through her port. Everything went smooth and they were home just before 3pm and we all walked over to get Ryley from school.
Tuesday evening Karlee got to go to bring a friend night at the Bridlewood Beaver colony as Erica’s friend. She has a great time and enjoyed all the fun activities. She is looking forward to being a Beaver next year and is especially excited about going camping in the fall. Next year should be exciting with Karlee joining Beavers and Ryley moving up to cubs. Jennifer is going to be a cub leader while Dad stays with the Beavers to spend some time with Karlee.
Wednesday was Karlee’s first day at Jamie’s Preschool. Jamie’s Preschool caters to kids dealing with cancer and auto-immune deficiency diseases. It offers a cold and flu free environment where Karlee can go to get some socialization with other kids. It didn’t seem to be a big deal that she wasn’t in school at the start of the year when she wasn’t feeling well, but now that she is feeling better we could tell she was missing the socialization. She will go to preschool Tuesday and Wednesday from 12:15 – 2:45 and Thursday’s they start with Gymnastics from 11:30 – 12:30 and then school from 12:45 – 2:45. Mom dropped her off at 12:15 and the first thing they do is eat lunch. Karlee was a little shy at first, but by the end she was a little social butterfly (according to one of the other parents) and was enjoying herself. She really enjoyed the crafts and is now looking forward to preschool.
Wednesday night Karlee and Mom went to our Lifegroup potluck while Ryley and Dad headed to his hockey game. Mom and Karlee had a good time with everyone and Ryley’s team played a great game.
Thursday was gymnastics for Karlee’s preschool. Ryley was invited along as they encourage siblings to attend events like this so they don’t feel left out or excluded and it is teacher’s convention for him. After a little driving around and a trip around the building to find the door we got into Stars Gymnastics on the old Currie Barracks. They had several staff members helping the kids through the various stations and everyone had a great time. It was also a nice chance to visit with other parents and grandparents of kids who had gone through something very similar to our experience. There is one little boy, Levi, who is 5 and has been off maintenance for a while after going through treatment for ALL. It is nice to talk to his Mom and know that there is an end to everything.
Thursday night was another hockey game. It was also the first game of the year that Dad got to watch without being behind the bench or in the timekeepers box. Karlee behaved wonderfully so Dad could actually watch most of the game. It was another good game with us winning again. Mom did her normal Thursday night yoga again out at Red Deer Lake Community Centre.
Friday was another day off for both kids. We took Ryley to Harry Potter at the cheap theatre’s after Dad was done work. We tried to get to it a couple times during Christmas, but with everything going on it was just too difficult to find the time. Ryley jumped several times during the movie, but overall he enjoyed it. Karlee went over to Grandma’s and watch a movie and played dollies.
I have uploaded a bunch of other pictures of gymnastics on Facebook. It looks like we will have a busy weekend with 2 hockey practices, a hockey game, the Heritage Classic and the Hitmen Outdoor game!
Tuesday evening Karlee got to go to bring a friend night at the Bridlewood Beaver colony as Erica’s friend. She has a great time and enjoyed all the fun activities. She is looking forward to being a Beaver next year and is especially excited about going camping in the fall. Next year should be exciting with Karlee joining Beavers and Ryley moving up to cubs. Jennifer is going to be a cub leader while Dad stays with the Beavers to spend some time with Karlee.
Wednesday was Karlee’s first day at Jamie’s Preschool. Jamie’s Preschool caters to kids dealing with cancer and auto-immune deficiency diseases. It offers a cold and flu free environment where Karlee can go to get some socialization with other kids. It didn’t seem to be a big deal that she wasn’t in school at the start of the year when she wasn’t feeling well, but now that she is feeling better we could tell she was missing the socialization. She will go to preschool Tuesday and Wednesday from 12:15 – 2:45 and Thursday’s they start with Gymnastics from 11:30 – 12:30 and then school from 12:45 – 2:45. Mom dropped her off at 12:15 and the first thing they do is eat lunch. Karlee was a little shy at first, but by the end she was a little social butterfly (according to one of the other parents) and was enjoying herself. She really enjoyed the crafts and is now looking forward to preschool.
Wednesday night Karlee and Mom went to our Lifegroup potluck while Ryley and Dad headed to his hockey game. Mom and Karlee had a good time with everyone and Ryley’s team played a great game.
Thursday was gymnastics for Karlee’s preschool. Ryley was invited along as they encourage siblings to attend events like this so they don’t feel left out or excluded and it is teacher’s convention for him. After a little driving around and a trip around the building to find the door we got into Stars Gymnastics on the old Currie Barracks. They had several staff members helping the kids through the various stations and everyone had a great time. It was also a nice chance to visit with other parents and grandparents of kids who had gone through something very similar to our experience. There is one little boy, Levi, who is 5 and has been off maintenance for a while after going through treatment for ALL. It is nice to talk to his Mom and know that there is an end to everything.
Thursday night was another hockey game. It was also the first game of the year that Dad got to watch without being behind the bench or in the timekeepers box. Karlee behaved wonderfully so Dad could actually watch most of the game. It was another good game with us winning again. Mom did her normal Thursday night yoga again out at Red Deer Lake Community Centre.
Friday was another day off for both kids. We took Ryley to Harry Potter at the cheap theatre’s after Dad was done work. We tried to get to it a couple times during Christmas, but with everything going on it was just too difficult to find the time. Ryley jumped several times during the movie, but overall he enjoyed it. Karlee went over to Grandma’s and watch a movie and played dollies.
I have uploaded a bunch of other pictures of gymnastics on Facebook. It looks like we will have a busy weekend with 2 hockey practices, a hockey game, the Heritage Classic and the Hitmen Outdoor game!
Sunday, February 13, 2011
Lots of Happenings
Thursday was a quick day at the hospital… well as quick as can be expected. We left home and dropped Ryley off at school after lunch, made a quick stop and then headed up to the hospital. Parking was a little better Thursday, but the telethon was still going on so there wasn’t much to pick from. After a couple of loops around the lower level we managed to find a spot and were in the clinic on time for our 2pm appointment. We played a little Mario on the DS and chatted with another family in there and were in the back about 2:25 or so. They didn’t feel she needed to be assessed so they just deaccessed her and sent us on our way home. It was a nurse we had never had before, but like the trooper she is Karlee had no problems and the nurse was great like all the nurses in the clinic and on the unit.
On the way home we stopped by the KCCFA office to drop off some scrubbies and pick up some slipper money. Everyone was great there and was excited to see Karlee without her hair. They were excited about the upcoming skate-a-thon for Karlee and the KCCFA. We had a really nice visit, but unfortunately Mary was out of the office that day sick. Jennifer will have to stop in again to say “Hi!” to Mary after another clinic day.
Friday night was the unparented Beaver sleepover. We had 36 Beavers for pizza, crafts,a movie, sleepover and breakfast. Most of the parents were a little nervous about leaving their 5 to 7 year olds overnight, but overall the night went excellent and I think everyone had a wonderful time. I know Ryley enjoyed himself and I did my best to leave him alone so he would get the benefit of not having a parent hovering over him all the time.
Saturday morning the story about the Skate-A-Thon ran in the Calgary Herald so we had to stop on the way home from the sleepover to pick up a couple papers. Here is a link to the story: http://www.calgaryherald.com/health/Girl+cancer+fight+inspires+Lightning+Bolts+skate+thon/4270962/story.html. Ryley’s hockey team really is an incredible group of kids and parents. I have heard from a number of different people who will be skating and some other teams who are handing out pledge forms to their teams. We are really looking forward to this event and enjoying the support from all our friends and other people we do not know.
Saturday evening we dropped the kids off at Grandma’s and headed to Jennifer’s cousin Danny’s 30th birthday party. It was a great time and was a special night for Danny and his girlfriend Eva. They announced that they were engaged and would be getting married this summer. It sounds like they are going to have a wedding in Indonesia and another one in Calgary when they return.
Sunday morning we went to Church for the first time since before Christmas. Karlee was finally feeling up to going out and Ryley didn’t have hockey. It was nice to see everyone again and catch up with some people. Hopefully after hockey season we will be able to get to a normal schedule. Sunday evening we went to Grandma’s for dinner with the family. It was nice to finally see everyone there again as we have had to miss the last 3 weeks due to hockey or sickness.
Sunday evening we called about getting Karlee into Jamie’s Preschool for kids with cancer and other supressed immune systems. Mom had a nice 30 minute chat with Liz from the preschool and it sounds like this may be a great fit for Karlee. We are thinking of starting her on Wednesday so she has a day to recover after Monday treatment. Karlee would go 3 days a week – Tuesday – Thursday from 12:15 to 2:45. It sounds like they offer an excellent program with lots of diversity. Wednesday’s are music day and Thursdays they start out at the Gymtastics location and then go back to the school. Tomorrow Mom is going to talk to Karlee and make sure this is something she wants to do and they we will see what happens.
On the way home we stopped by the KCCFA office to drop off some scrubbies and pick up some slipper money. Everyone was great there and was excited to see Karlee without her hair. They were excited about the upcoming skate-a-thon for Karlee and the KCCFA. We had a really nice visit, but unfortunately Mary was out of the office that day sick. Jennifer will have to stop in again to say “Hi!” to Mary after another clinic day.
Friday night was the unparented Beaver sleepover. We had 36 Beavers for pizza, crafts,a movie, sleepover and breakfast. Most of the parents were a little nervous about leaving their 5 to 7 year olds overnight, but overall the night went excellent and I think everyone had a wonderful time. I know Ryley enjoyed himself and I did my best to leave him alone so he would get the benefit of not having a parent hovering over him all the time.
Saturday morning the story about the Skate-A-Thon ran in the Calgary Herald so we had to stop on the way home from the sleepover to pick up a couple papers. Here is a link to the story: http://www.calgaryherald.com/health/Girl+cancer+fight+inspires+Lightning+Bolts+skate+thon/4270962/story.html. Ryley’s hockey team really is an incredible group of kids and parents. I have heard from a number of different people who will be skating and some other teams who are handing out pledge forms to their teams. We are really looking forward to this event and enjoying the support from all our friends and other people we do not know.
Saturday evening we dropped the kids off at Grandma’s and headed to Jennifer’s cousin Danny’s 30th birthday party. It was a great time and was a special night for Danny and his girlfriend Eva. They announced that they were engaged and would be getting married this summer. It sounds like they are going to have a wedding in Indonesia and another one in Calgary when they return.
Sunday morning we went to Church for the first time since before Christmas. Karlee was finally feeling up to going out and Ryley didn’t have hockey. It was nice to see everyone again and catch up with some people. Hopefully after hockey season we will be able to get to a normal schedule. Sunday evening we went to Grandma’s for dinner with the family. It was nice to finally see everyone there again as we have had to miss the last 3 weeks due to hockey or sickness.
Sunday evening we called about getting Karlee into Jamie’s Preschool for kids with cancer and other supressed immune systems. Mom had a nice 30 minute chat with Liz from the preschool and it sounds like this may be a great fit for Karlee. We are thinking of starting her on Wednesday so she has a day to recover after Monday treatment. Karlee would go 3 days a week – Tuesday – Thursday from 12:15 to 2:45. It sounds like they offer an excellent program with lots of diversity. Wednesday’s are music day and Thursdays they start out at the Gymtastics location and then go back to the school. Tomorrow Mom is going to talk to Karlee and make sure this is something she wants to do and they we will see what happens.
Wednesday, February 9, 2011
Hospital Visit
The last blog I forgot to give everyone an update on Ryley. He got his first hockey goal of the year on Sunday night. Of course this was the first game that Dad missed this year as he was attending a Scout meeting and Mom was taking Karlee to the bathroom. He seems to have forgiven us and is still revelling in his first goal.
Tuesday we got an e-mail from Jo asking us to bring Karlee in on Friday to see where her numbers are and to, hopefully, continue treatment. We asked if we could bring her to the lab on Thursday and get her CBC done and come to the hospital on Friday only if she is able to start treatment. Since Karlee needs to have a lumbar puncture (and needs to be put under) we don’t want her to fast until they decide if she can start treatment.
So it looks like Thursday is now on hold as Karlee was up at the clinic today for a CBC and some IV antibiotics. Tuesday night Karlee was up just before midnight vomiting and complaining about her tummy not feeling good. She wasn’t up for too long, but didn’t have the best nights sleep. She was up a couple of times and just didn’t seem to be comfortable most of the night. Wednesday morning she stayed home with Dad since Mom was doing the bus run and then was going into Ryley’s school for home reading. She was a little warm most of the morning and a couple of times was running a fever. We called Jo around noon and finally go through to her about 1. We were instructed to bring her up just to get everything checked out and make sure she was ok.
While Mom was talking to Jo we were also talking to a reporter with the Calgary Herald. They want to do a story about the Skate-A-Thon for Karlee and the KCCFA. Dad spent about 30 minutes talking to the reporter on the phone and gave her some other people to talk to and sent her a few photos of the team and Karlee. The Skate-A-Thon is looking to be a huge success and will be a fun time for everyone. There is still room for more skaters so if anyone is interested let me know and I will put you in contact with the correct people. We are also still looking for prizes for both kids and adults. Again if you can help with that drop me an e-mail at ronlewis@telusplanet.net. Ryley is still looking for pledges so it you are interested you can drop of cash or cheques to us or give us a call and we can pick them up. It is sounding like there are going to be some great door prizes or bucket draws so hopefully lots of people can come out on February 27th at 3:15 –4:15 at the South Calgary Rec Centre.
Karlee and Mom were up at the hospital on the unit this afternoon and got her CBC and some IV antibiotics. Her counts are looking better, but are starting to get too high which can mean other things. We have seen her counts spike before and they have gone down again rapidly so hopefully this is another short abnormality. The unit is on lock down right now due to some of the stuff that is going around. That means that only one parent is allowed in and everyone has to stay in their rooms. Fortunately they were out of the unit just after pizza time and didn’t have to deal with the restrictions for too long. Ryley had a great workout tonight at Skillz with his hockey team.
After the last blog entry with all the links and other interesting information I was given more information about another great cycling fund raiser this summer. The KCCFA has their own tour which is one of very few allowed on the Icefield highway. This tour is also stopping at Camp Kindle this summer for one of the nights of camping. This is a great event with 100% of the money raised going to the KCCFA. Check out www.tourforkids.ca for more information.
Tomorrow Dad is going to take Karlee up for an assessment and maybe another dose of IV antibiotics. They should also let us know if we are going to start treatment on Friday or Tuesday. Hopefully we have a nice quick day tomorrow and are home in lots of time for Mom to go to Yoga and relax.
Tuesday we got an e-mail from Jo asking us to bring Karlee in on Friday to see where her numbers are and to, hopefully, continue treatment. We asked if we could bring her to the lab on Thursday and get her CBC done and come to the hospital on Friday only if she is able to start treatment. Since Karlee needs to have a lumbar puncture (and needs to be put under) we don’t want her to fast until they decide if she can start treatment.
So it looks like Thursday is now on hold as Karlee was up at the clinic today for a CBC and some IV antibiotics. Tuesday night Karlee was up just before midnight vomiting and complaining about her tummy not feeling good. She wasn’t up for too long, but didn’t have the best nights sleep. She was up a couple of times and just didn’t seem to be comfortable most of the night. Wednesday morning she stayed home with Dad since Mom was doing the bus run and then was going into Ryley’s school for home reading. She was a little warm most of the morning and a couple of times was running a fever. We called Jo around noon and finally go through to her about 1. We were instructed to bring her up just to get everything checked out and make sure she was ok.
While Mom was talking to Jo we were also talking to a reporter with the Calgary Herald. They want to do a story about the Skate-A-Thon for Karlee and the KCCFA. Dad spent about 30 minutes talking to the reporter on the phone and gave her some other people to talk to and sent her a few photos of the team and Karlee. The Skate-A-Thon is looking to be a huge success and will be a fun time for everyone. There is still room for more skaters so if anyone is interested let me know and I will put you in contact with the correct people. We are also still looking for prizes for both kids and adults. Again if you can help with that drop me an e-mail at ronlewis@telusplanet.net. Ryley is still looking for pledges so it you are interested you can drop of cash or cheques to us or give us a call and we can pick them up. It is sounding like there are going to be some great door prizes or bucket draws so hopefully lots of people can come out on February 27th at 3:15 –4:15 at the South Calgary Rec Centre.
Karlee and Mom were up at the hospital on the unit this afternoon and got her CBC and some IV antibiotics. Her counts are looking better, but are starting to get too high which can mean other things. We have seen her counts spike before and they have gone down again rapidly so hopefully this is another short abnormality. The unit is on lock down right now due to some of the stuff that is going around. That means that only one parent is allowed in and everyone has to stay in their rooms. Fortunately they were out of the unit just after pizza time and didn’t have to deal with the restrictions for too long. Ryley had a great workout tonight at Skillz with his hockey team.
After the last blog entry with all the links and other interesting information I was given more information about another great cycling fund raiser this summer. The KCCFA has their own tour which is one of very few allowed on the Icefield highway. This tour is also stopping at Camp Kindle this summer for one of the nights of camping. This is a great event with 100% of the money raised going to the KCCFA. Check out www.tourforkids.ca for more information.
Tomorrow Dad is going to take Karlee up for an assessment and maybe another dose of IV antibiotics. They should also let us know if we are going to start treatment on Friday or Tuesday. Hopefully we have a nice quick day tomorrow and are home in lots of time for Mom to go to Yoga and relax.
Monday, February 7, 2011
The Bigger Picture
This has been a pretty boring week with Karlee not being allowed to visit anyone or go anywhere. Today was her CBC at the South Calgary Lab and, of course, a nice little snow storm. We got about 6 inches of snow overnight and this morning. Mom’s bus run took a little longer than normal, but was still home in enough time to take Karlee for her blood work. When they came in the volunteer at the front desk greeted them for the 3rd week in a row. When they left she said, “See you next week.” Maybe that was a sign of things to come…
Once they returned it was again the waiting game – waiting for the phone call from Jo to tell us if she gets to continue treatment or if she is still delayed. Karlee really wanted to go with Mom on the bus run this afternoon so she was waiting patiently for the call. Of course the call didn’t come in time so she had to stay home again. We got the call around 4:30 and Karlee’s counts are still too low for her to start the next phase. Her ANC has come up to 600, but she needs to be over 750 to start the next round. Jo also wants to make sure she is well over 750 if we can get her up there. In this round they increase the dosage and challenge her with more drugs each session so she needs to be good and ready or will end up delayed in the middle of the phase.
Karlee is now off house arrest, but still can’t be out in close contact with other people. She was going to go to Bring A Friend Night with the Beavers tomorrow night, but now has to stay home again. We have booked another CBC for next Monday; hopefully that will be the last blood work at a lab for a little while.
I thought I would share some of the links and stories that have inspired us. Just so everyone understands not all the stories have happy endings, but in some ways these are the most inspiring. To see how a family can come through something as tragic as loosing a child to this awful disease and at the same time remain positive and help other people, is just as incredible as a family that makes it through their battle successfully.
We came across this video recently that was posted by the nurse at the Kids Cancer Care Foundation on Facebook. Megan McNeil was a childhood cancer patient who lost her battle with cancer about a week ago. She wrote a beautiful song to help patients in their battle and the cause was taken up by producer Garth Richardson. The result is a very moving and inspirational song that is raising funds for childhood cancer research and to support families going through this. All the singers in the video are childhood cancer patients which makes it even hard hitting. Please check out the video on YouTube and the Website. It is a great song and well worth the 99 cents on iTunes.
Megan’s Video:
http://www.youtube.com/watch?v=Y9pHISnIj2Y
Will to Survive Website:
http://www.willtosurvive.org/
When we were at camp there was a little boy, Alexander, who we saw several times. At the KCCFA kids Halloween party they let balloons go as a celebration of his life as he had recently lost his battle with cancer. Recently we found his web page on the internet and were very moved by his story and what his family is doing to help other kids with terminal cancer. This is another story of a family that has suffered more than anyone should ever have to, but has come through with a desire to help others going through similar events.
Alexander’s Quest – Little Wishes for Little Warriors
http://www.alexandersquest.ca/
Chloe is another little girl we met at the Alberta Children’s Hospital. Her story is fairly similar to Karlee’s and reading her blog is a nice way to know that there are other people going through the same thing as we are.
http://www.caringbridge.org/visit/chloedavidson
There is also a website that lists blogs and webpages for other kids who are battling leukemia, some who have lost their battle and many who have beaten this ugly disease. Reading these is very therapeutic in various ways. Many times it lets us know that we have it pretty easy compare to some; it lets us see the light at the end of the tunnel by reading so many of the success stories and reading about all the similar experiences we have all been going through.
http://www.acor.org/ped-onc/hp/leukpages.html
We have a friend who has been very moved by Karlee’s story and has decided to ride in the Enbridge Ride to Conquer Cancer and raise money for the Canadian Cancer Society. Please take a look at his website and his blog:
http://web.me.com/kelsomurray/RTCC_2011_-_Russell/About_Me.html
These are some of the links and resources we are using to stay positive and informed through this journey. We did a Q&A type of blog entry a while ago, but if anyone has any questions let us know and we could do another one as many people enjoyed it. E-mail your questions to ronlewis@telusplanet.net.
Once they returned it was again the waiting game – waiting for the phone call from Jo to tell us if she gets to continue treatment or if she is still delayed. Karlee really wanted to go with Mom on the bus run this afternoon so she was waiting patiently for the call. Of course the call didn’t come in time so she had to stay home again. We got the call around 4:30 and Karlee’s counts are still too low for her to start the next phase. Her ANC has come up to 600, but she needs to be over 750 to start the next round. Jo also wants to make sure she is well over 750 if we can get her up there. In this round they increase the dosage and challenge her with more drugs each session so she needs to be good and ready or will end up delayed in the middle of the phase.
Karlee is now off house arrest, but still can’t be out in close contact with other people. She was going to go to Bring A Friend Night with the Beavers tomorrow night, but now has to stay home again. We have booked another CBC for next Monday; hopefully that will be the last blood work at a lab for a little while.
I thought I would share some of the links and stories that have inspired us. Just so everyone understands not all the stories have happy endings, but in some ways these are the most inspiring. To see how a family can come through something as tragic as loosing a child to this awful disease and at the same time remain positive and help other people, is just as incredible as a family that makes it through their battle successfully.
We came across this video recently that was posted by the nurse at the Kids Cancer Care Foundation on Facebook. Megan McNeil was a childhood cancer patient who lost her battle with cancer about a week ago. She wrote a beautiful song to help patients in their battle and the cause was taken up by producer Garth Richardson. The result is a very moving and inspirational song that is raising funds for childhood cancer research and to support families going through this. All the singers in the video are childhood cancer patients which makes it even hard hitting. Please check out the video on YouTube and the Website. It is a great song and well worth the 99 cents on iTunes.
Megan’s Video:
http://www.youtube.com/watch?v=Y9pHISnIj2Y
Will to Survive Website:
http://www.willtosurvive.org/
When we were at camp there was a little boy, Alexander, who we saw several times. At the KCCFA kids Halloween party they let balloons go as a celebration of his life as he had recently lost his battle with cancer. Recently we found his web page on the internet and were very moved by his story and what his family is doing to help other kids with terminal cancer. This is another story of a family that has suffered more than anyone should ever have to, but has come through with a desire to help others going through similar events.
Alexander’s Quest – Little Wishes for Little Warriors
http://www.alexandersquest.ca/
Chloe is another little girl we met at the Alberta Children’s Hospital. Her story is fairly similar to Karlee’s and reading her blog is a nice way to know that there are other people going through the same thing as we are.
http://www.caringbridge.org/visit/chloedavidson
There is also a website that lists blogs and webpages for other kids who are battling leukemia, some who have lost their battle and many who have beaten this ugly disease. Reading these is very therapeutic in various ways. Many times it lets us know that we have it pretty easy compare to some; it lets us see the light at the end of the tunnel by reading so many of the success stories and reading about all the similar experiences we have all been going through.
http://www.acor.org/ped-onc/hp/leukpages.html
We have a friend who has been very moved by Karlee’s story and has decided to ride in the Enbridge Ride to Conquer Cancer and raise money for the Canadian Cancer Society. Please take a look at his website and his blog:
http://web.me.com/kelsomurray/RTCC_2011_-_Russell/About_Me.html
These are some of the links and resources we are using to stay positive and informed through this journey. We did a Q&A type of blog entry a while ago, but if anyone has any questions let us know and we could do another one as many people enjoyed it. E-mail your questions to ronlewis@telusplanet.net.
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