Skip to main content

Today's CF Climb & a few ?s

Racing up 58 Flights For Me:

Aw, isn't he sweet! Andrew (my Boyfriend) raced up the 58 flights of stairs in Chicago at the Cf Climb to raise money for our Team ("like" our Facebook Page)! He raised $425 today and did an amazing job! I'm soo proud of him! To read about last year's climb (for pics) click here for CF Climb 2013!

Right Pic: Andrew enjoying the breakfast and fueling up before the climb! Below: Andrew's time recorded! 

This year Andrew did it in 22 minutes and 13 seconds! Which means his avearge (if I did the math right) was
22.9 seconds per flight! He may have been a little disappointed since his time was slower than last year, but I think at least some of that had to do with the way they had the people line up this year.


Pic Right: Andrew just coming out of the stairwell... 

Last year they announced 3 groups to line up to sort of divide the people up. This way the fastest people were first and didn't have to go around slower climbers. First group is Elite: under 10 minutes, 2nd group is Competitive: under 20 minutes( the group Andrew anticipated) and then recreational for people like me. Andrew was planning on trying to be at the front pack of the competitive group. However, when they announced it this year it they said the time for the 2nd group was an end time of 13 minutes. Since Andrew's goal time was 17 minutes, he figured he'd go in the next group. But it turns out they didn't add another group, just had everyone wanting over 13 minutes go as "recreational". And Andrew was in the middle of the pack. There were over 260 some runners (so probably middle of a group of 100 people). So even though he was discouraged a little, when he told me the first 10 flights were him trying to pass people in the stairwell to get ahead of them, I realized he probably lost a least a few minutes trying to get around the mass of children, and people who like me (intended to take their time).

So don't be hard on yourself Andrew, you did amazing and I'm very proud! I really wanted to do it this year, but with my stomach surgery scar just fully healing now (sort of done ish), I'm not quite ready for that climb!
We did get our picture taken together though!

However, I do plan on doing it next year and if anyone wants to do it "recreationally". Walk as slow as we want and stop every 5 floors for my small coughing attacks, let me know! I'd love to have some climbing buddies. :-)

Make sure to check the older post (below) I added the promo video we did (and it will give you a taste of what Andrew did today)! Not only did he run up 58 flights for CF, he did it for me. AND in the process raised another $425 for CF research. This brings our total up to $14,526 for the year of 2014! check out how much we raised at each function: on this Page HERE! 

Please do take the time to check out that page, it has lots of great info and has a full list of the events I want to attend next year. I travel to multiple sites so friends in other cities (like U of I buddies in Champaign), can be involved too! So if you want to walk in your city, let me know. Also, you can join in for Chicago's FestivAle (if you would enjoy a night of food & beer) AND of course I'd love for EVERYONE to come to Princeton's NEW Great Strides Walk! So if you want to join at any of these events let me know. More dates will be posted in the next month or two!

So thank you to everyone who helped make this happen today! What an amazing day for Team CF2! I can't believe how much just my family, friends, and community could raise for research and how much support the CF community has received from them!

I have a lot of walkers who have dedicated their time to more than one event over many years! So much to love everyone! THANK YOU!

Which CF Walk Location/ CF Event you have done is your favorite and why? (this will also help me make our Princeton Walk better- with new ideas). So please leave your comment below or on the FB comments. 




Comments

Popular posts from this blog

5K. I could cry. Beyond Annoyed.

My 5K I paid my registartion fee weeks ago, have been training and I'm ready for the 5K. However, I didn't get to run my 5K today. Why? Because Cystic Fibrosis decided to one up me. I got my spots back friday, and they just got worse and worse. They look like this: They take over my feet, and sometimes my calves. I posted about this a few weeks ago. I had them during the last few performances of Hairspray. I call it the "Mummy disease" because when it happens my joints freeze up and I can't move. So the morning of my 5K I wake up and they are on my thighs...     and on my arms. This is the worst they have been in years. I took pictures to show Dr. B at my clinic on the 11th.  I'm just really bummed and upset about my weekend! I was supposed to run my first 5K!!!!! I then had a bags tournament in Peoria for the Dream Factory, and was then going to head to Champaign for Sat night- Monday! My friend Alex, reserved me a ticket for Ren...

Calling All Who Care!

     Please Read : Okay, so first off I want to say that this post is tough. It's tough to think about and write. However, it is extremely important and a huge topic in the CF Community, and is VERY NEAR AND DEAR to MY HEART!  First I want to ask you... What if I told you I needed a Transplant. That I needed to reach a certain weight, get my kindeys functioning better, get a higher pain tolerance, and get off a couple medications I take right now. What if I said I couldn't receive a 2nd chance at life unless I reached these goals and I raised a certain amount of money that seems impossible to raise. What if I had been in and out of the hospital off and on for the last year, with many surgeries, had multiple infections and my lung function dropped from 40s to the teens and now is slowly dropping still. What if I was starting to wonder if my decision to go through the grueling Transplant tests was worth it. What if I start to get down about my cf and wondering why ev...

A Hospital at Home

Coming home from the hospital takes a balance..... Wait.... Did I just say home from the hospital??? That's right!  I get to leave Wednesday the 18th, after 8 days in the hospital. It was a logistical thing. I have a super important court date on for "Shoes (our AMAZING foster son) soon." So Doc knew before he admitted me that I would be leaving by that day... So what does this mean for me and my health??? Well, I need to make sure I continue the same treatment schedule I would in the hospital. So 4 sets of nebs a day. 8am, noon, 4pm, 8pm. Which means I finish my course of IVs at home. I will be on IV's at least until 27th (so 1.5 weeks left). I came into the hospital on Tuesday the 10th, but we didn't realize until Friday the 13th that my Psuedomonas is resistant to all of the antibiotic options for IVs except one med. So on the 13th we switched to Avycaz, which is a newer, hard hitting antibiotic that was brought to market less than 3 years ago. We were hoping I...