Skip to main content

Golf for a Cure & Other Fundraisers

Fundraisers & More:

Yesterday was a great day! Andrew and I attended the Suzanna Lee Memorial Silver Cup Challenge, Golf Outing for the Cystic Fibrosis Foundation. It is one of the Peoria CFF Chapter's yearly events and this year was the Golf Outing's 15th year!

Everyone arrives around 11am for the grilled outdoor lunch before Tee time starts at noon. The Golfers are out for 4 hours golfing, some of the holes have competitions at them (like longest putt). During the golfing volunteers help set up the banquet dinner hall. There are over 100 silent auctions, chocolate fountain, hors d'oeuvres, followed by the dinner served between 5:30-6:30pm.

Andrew loved golfing and I enjoyed helping set up the silent auctions. I was the speaker this year and was very honored to the speaking about my life with Cystic Fibrosis. The Golf Outing was started 15 years ago in memory of Suzanna Lee (a girl who went to my CF Clinic and was from Peoria). Her parents host it every year and it raises a lot of the money for the CF Foundation!

I've uploaded my speech to YouTube here and I will be posting the Golf Outing Album in the next few days on my CF Facebook Awareness Page, make sure to check it out!

Now that the Golf Outing is over, it is time for me to hardcore focus on the Princeton CF Walk! We still need a few more teams to sign up. We lost 2 big teams from last year ( do to moving, etc). I'm excited for their new chapters in their lives, but we could use some help in reaching our Goal Amount! We have brought in around $5,000 so far online, but at this time last year we had raised over $10,000. We raised $23,000 last year and this year we are projected to only raise around $8,000-$10,000 this year!

Some ways you can help is donate, share, or join us walking and form your own team! Also, hosting a secondary supplemental fundraiser is very helpful. My uncles host a dessert party every year. They make some dessert, get some wine, and ask friends to bring checks made to the CF Foundation. They raised $375 in the past! My Aunt makes homemade Jam and sells it in her town & through me on Facebook, she raised almost $300 last year.  Here is the link to her Facebook event she made for it this year!

Also, contests work: For example: I will shave my beard off for $1,000! Really anything could be made into a fundraiser, so please consider doing one and help us out! I have some great ideas for next year to change it up & raise more, but we need to succeed this year in order for us to remain a CF official Great Strides Walk site!

Here is the online link to the CF Princeton Walk registration & info page: http://fightcf.cff.org/PrincetonGS

If you can help or want to start a team in Princeton please let me know! I can help you :-)

Thank you!!!!

Comments

Popular posts from this blog

How Fostering and CF impact my work

I haven't been on my blog much.... I think that is because most of my blogging is currently been done on Health Union's Cystic-Fibrosis.com (here is link to all my posts on their site: https://cystic-fibrosis.com/members/cherizkunkel/ ). I decided last fall to step away from real estate after 3 years in the business. It was tough to say good-bye, especially since I had tripled my volume and business in the last year. However, I didn't have time to add any new clients; I kept saying, maybe next week, next month I can fit more work into my schedule. The truth is fostering takes a lot of time. We have between 5-8 monthly visits at the agency, 1 court ate a month, 2 home visits from the caseworker a month, plus e have 2-3 doctors/specialist appointments for our current kiddo. We have lots of paperwork we fill out, gas mile logs, receipts to add, and more! Our kiddo also participates in gymnastics and dance two nights a week. We go to a fosterparent support group with our kid ...

Today's BIG Appointment

 I discussed last week about my recent struggles & goals. I have been dealing with a lot all at once! Family planning (update on that in 2 weeks), my Grandma's funeral, lower lung function. Through it all I have remained very compliant with my meds! My health is VERY important to me. So this last weekend I took my vest machine, wabi sterilizer system , and packs of ensure to my parent's for the weekend. I wanted to make sure I did everything. While it was a sad occasion, it was still pleasant seeing almost all of the family together again. Actually 27 out of 29 of the cousins made it to the funeral. Grandpa is in the middle of the picture (can you find me?) LOL   On top of my medications I have been doing some dancing & walking, but no jogging or anything. I'm still counting calories on my fitbit (hitting over 3000) a day (& 40 grams of protein, 50 grams of fat at least). I knew I was feeling a bit better than before, but wasn't sure what to expec...

Antibiotic Free Streak Over

Clinical Trial & Uh-Ohs: A lot happened this weekend. Thursday was my clinical trial and yay!!!!! my lung function was still same. It's 55% by Docs standards, but by the trial standard it would be considered 60 still. So don't freak out and think my lung function has dropped since I wrote the Blog Post  Welcome to the 60s (read it here) . So that's good news. In 2010, I was struggling in the high 30s and low 40s. Then in 2011 I switched to Doc B, also I was done with school. I had more time to focus on meds and exercise. My extra effort and my proactive doc brought my lungs up to 58  in 2011. And Thursday I was happy to see it at the same place. No decrease in 3 years!!!!! However, I've gotten into the mid 60s before. But that was only after hospitalizations and IV treatments. Well, in the last year I have been enrolling in a couple clinical trials. Most trials are 6 months long. I'm  currently in one now. Its a 3rd phase trial and the 2nd phase trials show...