I don't repost a lot on this blog, but this video really gets the point across very well.
2010 Great Strides Walk
We would like to invite you to come out to our annual walk for Cystic Fibrosis in honor of our son Colin. This year we are participating in our eighth walk to help find a cure for CF. Many things have changed since last year. First of all the date for our walk is in May this year. The walk will take place on Saturday, May 22, 2010 at the Naperville Riverwalk with an evening party option at our home as well.
The other big change this year is that we exhausted all of our attempts and options to help Colin to gain and maintain a healthy weight. After three long years of apprehension, we decided to take our doctor’s recommendation. Colin had a surgery this past November to insert a permanent feeding tube in his stomach. He now receives nightly feedings that amount to over 700 additional calories. The most exciting news for us is that this surgery and his recovery went very well and Colin has gained over 5lbs since November! The feeding tube adds quite a bit of work and time to Colin’s already busy routine of AM and PM treatments, medicines and therapies. However, we know we made the right decision and we are grateful that this technology and treatment is available to help our son.
The technology and treatments are what brings us to writing this very important letter and pleading for your continued help and support. Many important advancements and great strides in research have been made this past year because of your generous donations. However, there still is no cure for cystic fibrosis and we still need your help.
As always, we would love to see you out at the Naperville walk site. It is a really fun family day. If you cannot make it there come out to our house any time on the 22nd of May after 5pm. Most importantly, please donate whatever you can to the Cystic Fibrosis Foundation under Colin’s Clan to help find a cure.
Colin has really grown up a lot. He cannot wait for his soccer season to start and is having a great year in first grade. He loves school and has become quite the reader and writer! He also is really starting to become aware of all the amazing people who continue to work towards finding a cure for cf!!
Thank you in advance and we can’t wait to celebrate the advancements in CF research made possible by all of you. Please donate and help us find an end to this disease. Thank you so very much.
1. Online Donations (Press Click to Donate at the bottom)
2. Join our team (5/22 at Riverwalk Grand Pavilion) and donate at the walk (Press Join My Team at the bottom) Map
3. Come to our party and donate there. (Email me for info)
More Info:
http://www.curecfnow.com
http://www.colinsclan.com
http://www.cff.org
Thank you so very much,
The Walsh Family Chris, Trisha, Allison, Megan, and Colin
walsh.family@curecfnow.com
The other big change this year is that we exhausted all of our attempts and options to help Colin to gain and maintain a healthy weight. After three long years of apprehension, we decided to take our doctor’s recommendation. Colin had a surgery this past November to insert a permanent feeding tube in his stomach. He now receives nightly feedings that amount to over 700 additional calories. The most exciting news for us is that this surgery and his recovery went very well and Colin has gained over 5lbs since November! The feeding tube adds quite a bit of work and time to Colin’s already busy routine of AM and PM treatments, medicines and therapies. However, we know we made the right decision and we are grateful that this technology and treatment is available to help our son.
The technology and treatments are what brings us to writing this very important letter and pleading for your continued help and support. Many important advancements and great strides in research have been made this past year because of your generous donations. However, there still is no cure for cystic fibrosis and we still need your help.
As always, we would love to see you out at the Naperville walk site. It is a really fun family day. If you cannot make it there come out to our house any time on the 22nd of May after 5pm. Most importantly, please donate whatever you can to the Cystic Fibrosis Foundation under Colin’s Clan to help find a cure.
Colin has really grown up a lot. He cannot wait for his soccer season to start and is having a great year in first grade. He loves school and has become quite the reader and writer! He also is really starting to become aware of all the amazing people who continue to work towards finding a cure for cf!!
Thank you in advance and we can’t wait to celebrate the advancements in CF research made possible by all of you. Please donate and help us find an end to this disease. Thank you so very much.
1. Online Donations (Press Click to Donate at the bottom)
2. Join our team (5/22 at Riverwalk Grand Pavilion) and donate at the walk (Press Join My Team at the bottom) Map
3. Come to our party and donate there. (Email me for info)
More Info:
http://www.curecfnow.com
http://www.colinsclan.com
http://www.cff.org
Thank you so very much,
The Walsh Family Chris, Trisha, Allison, Megan, and Colin
walsh.family@curecfnow.com
2010 Naperville Great Strides
We would like to invite you to come out to our annual walk for Cystic Fibrosis in honor of our son Colin. This year we are participating in our eighth walk to help find a cure for CF. Many things have changed since last year. First of all the date for our walk is in May this year. The walk will take place on Saturday, May 22, 2010 at the Naperville Riverwalk with an evening party option at our home as well.
The other big change this year is that we exhausted all of our attempts and options to help Colin to gain and maintain a healthy weight. After three long years of apprehension, we decided to take our doctor’s recommendation. Colin had a surgery this past November to insert a permanent feeding tube in his stomach. He now receives nightly feedings that amount to over 700 additional calories. The most exciting news for us is that this surgery and his recovery went very well and Colin has gained over 5lbs since November! The feeding tube adds quite a bit of work and time to Colin’s already busy routine of AM and PM treatments, medicines and therapies. However, we know we made the right decision and we are grateful that this technology and treatment is available to help our son.
The technology and treatments are what brings us to writing this very important letter and pleading for your continued help and support. Many important advancements and great strides in research have been made this past year because of your generous donations. However, there still is no cure for cystic fibrosis and we still need your help.
As always, we would love to see you out at the Naperville walk site. It is a really fun family day. If you cannot make it there come out to our house any time on the 22nd of May after 5pm. Most importantly, please donate whatever you can to the Cystic Fibrosis Foundation under Colin’s Clan to help find a cure.
Colin has really grown up a lot. He cannot wait for his soccer season to start and is having a great year in first grade. He loves school and has become quite the reader and writer! He also is really starting to become aware of all the amazing people who continue to work towards finding a cure for cf!!
Thank you in advance and we can’t wait to celebrate the advancements in CF research made possible by all of you.
Please donate and help us find an end to this disease. Thank you so very much.
1. Online Donations: http://www.cff.org/Great_Strides/ChristopherWalsh5948 (Press Click to Donate at the bottom)
2. Join our team (5/22 at Riverwalk Grand Pavilion) and donate at the walk: http://www.cff.org/Great_Strides /ChristopherWalsh5948 (Press Join My Team at the bottom)
3. Come to our party and donate there.
A whole bunch of stuff I missed
As usual, I am behind in posting. I missed a whole lot of things between the Tri (post just below this one) and today. A few of the major points:
In late fall, Trisha held her second annual Naperville Uncork A Cure. Fantastic evening and we raised $50k for CFF that night. Gene Honda, announcer for the Sox, was our emcee and he did a fantastic job. Great guy. Along with Rosie Woods, I gave my first real bid for a cure speech. I am a huge fan of the bid speeches, just not from me. It was emotional, but it worked out for the best. I'll put a separate post out on this with pictures when I get a chance.
In late November, we finally were backed into a corner and Colin went in for surgery to get a G-Tube. We fought it for three years, looking for alternatives and maybe sometimes denying that he really needed it. The surgery was a little rough on him, as was the first day of recovery, but since then, he has gained his first pounds in over two years. He gained five in the first 45 days. This deserves its own post...again, I will get to it later, with pictures.
Working on the Sixth Annual Casino Chicago (http://www.cfholdem.com). Check out the site, this is a fantastic night.
For good and bad, we have met a lot of new cf families in the last few months. We've probably scared one or two by talking to them, but we try to give is as straight as possible.
I'll try to spend some time with real posts for the items above. They all deserve a little space (even if no one reads this thing).
In late fall, Trisha held her second annual Naperville Uncork A Cure. Fantastic evening and we raised $50k for CFF that night. Gene Honda, announcer for the Sox, was our emcee and he did a fantastic job. Great guy. Along with Rosie Woods, I gave my first real bid for a cure speech. I am a huge fan of the bid speeches, just not from me. It was emotional, but it worked out for the best. I'll put a separate post out on this with pictures when I get a chance.
In late November, we finally were backed into a corner and Colin went in for surgery to get a G-Tube. We fought it for three years, looking for alternatives and maybe sometimes denying that he really needed it. The surgery was a little rough on him, as was the first day of recovery, but since then, he has gained his first pounds in over two years. He gained five in the first 45 days. This deserves its own post...again, I will get to it later, with pictures.
Working on the Sixth Annual Casino Chicago (http://www.cfholdem.com). Check out the site, this is a fantastic night.
For good and bad, we have met a lot of new cf families in the last few months. We've probably scared one or two by talking to them, but we try to give is as straight as possible.
I'll try to spend some time with real posts for the items above. They all deserve a little space (even if no one reads this thing).
Team CF at the Chicago Triathlon and meeting with Steve
The day after our racing adventure, we headed to downtown Chicago to see Colin's uncles in the Chicago Triathlon. Uncle Bryan was competing in the triple - three tris in 24 hours. Insane, I know. Uncle Mark was competing in the tri for Team CF. Both did great and we're always proud to see them doing their part to find a cure.
At the finish line, we bumped into Steve Ferkau. I doubt it was a total accident, Steve probably saw the CFF banners or knew someone competing. Steve is an amazing guy. Probably one of the most uplifting people we know, in fact. Steve has cf and about nine years ago, received new lungs. He was at 10% capacity at the time, wheelchair bound, and the outlook wasn't good. He had been passed over or the opportunity fell through a number of times for other lung transplants for him. Then, he received his gift. Unlike some transplants, this wasn't just an insert of a new organ and Steve went on his merry way. Steve received his lungs from a teen in Iowa who was killed in an accident. Steve made the connection with the family and to this day he carries around pictures and articles of the girl that saved his life. Within a couple months of the new lungs, Steve was climbing stairs at work that seemed an Everest to him in the past. Not only that, but he started doing the stair climbs in Chicago: Aon, Hancock, etc. He leads Kari's Klimbers in those stair climbs and raises a lot of money for organ transplant organizations. He tells this story way better than I do, so I encourage you to check it out here. And I highly recommend that you stop and talk to him the next stair climb you see him at. You'll never talk to a happier, more upbeat person.
Racing to a Cure
Last week, we were asked by CFF if Colin would like to head out to Chicagoland Speedway and meet with a real racecar driver. We jumped at the chance. The backstory: Beasley Allen is a national law firm. They have someone on staff with cf and to show their support, they give CFF a spot on their car for publicity. At the towns they visit for races, they try to put together a meet and greet with a local cf family. We happened to be that family in Chicago and we couldn't have been more thrilled.
We met the kids as they were getting out of school at 2:30 and headed as fast as we could to Joliet to meet up with Grant Enfinger, who drives car 83. He's also the mechanic, the rig driver, the janitor, you name it. He was an exceptionally nice guy and showed Colin around the car and even let him sit in it.
The PR woman mentioned that we could visit the winner's circle if Grant won the race that night. We figured it was a long shot, more of a tease than anything, but we hung out for the race.
Grant started the race in a position in the high teens, maybe even low twenties. On the final lap, he was in second place, a hair behind the leader. He crossed the finish line just a 1/2 length behind the winner. never have we been so involved in a race, jumping up and down and cheering him on the entire way. It was pretty exciting.
I was thinking about the race and realized that it's a lot like cf and fundraising to find a cure. Both are a long race. They take a lot of money, determination, drive, and it takes the best to even stay in the race, much less win it. In the end, Grant hasn't yet won, just like we haven't won, but he was so close. It was in sight, he could taste it, he could see the checked flag, but he hasn't yet won. Just like us. His day will come, and so will ours.
It reminded me of a story that was told to us at the very first event we attended for cf about seven years ago. We were the guests of the chair family, even though they had never met us. They wanted us to see a big event because someone saw potential in us way back then (or they saw suckers about to dive in head first into a whole lot of work - poh-ta-toe/pa-ta-tow). Anyway, the chair, a really down to earth, realistic guy sat us down and told us his view of this damn disease. It also had a car theme.
Cf is a car racing down the road. This is no Yugo or Bug. It's a big, old eight cylinder 4 ton caddy. Our kids are playing in the road. We'd do anything for our kids to push them out of the way of that barreling car, but there just is no way to put yourself in that position. There's no pushing them out of the way, there's no taking their place. So instead, we fundraise. We grab the bumper of that car (we fundraise) and we tell all of our friends to help us grab that car bumper. We dig our heels in and we don't let go. We're doing everything we can to slow that car down and give the scientists time to find a cure.
Whether it's a race that we almost just won or whether we're grabbing the bumper to slow the car down, we're super close. It's coming. It's going to happen in Colin's lifetime and it's going to happen soon enough that he'll be able to live to an age where he can almost forget it ever happened. Maybe he'll be racing cars....who knows, he has a long full life to decide.
Uncork A Cure
Please join us on November 7, 2009 at Maggiano's in Naperville for our second annual Uncork-A-Cure benefiting the Cystic Fibrosis Foundation. More info coming soon.
09/06/09 Update: We now have tickets for sale online. There's an early bird discount, so please go out today and buy your tickets at UncorkACure.com
09/06/09 Update: We now have tickets for sale online. There's an early bird discount, so please go out today and buy your tickets at UncorkACure.com
Subscribe to:
Posts (Atom)