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!!!!

Labels:

Comments

Post a Comment

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 ...
2 comments
Read more

Oh the Joys of a Colonoscopy!

Colonoscopy, Fun: As you may remember from reading my October Posts (  Oct Post #1   &  2nd Oct Post ) that I was admitted a second time that month for Gastrointestinal issues. I was having stomach cramps and what was believed to be Antibiotic Associated Diarrhea. However, CT scan revealed my colon and intestines were inflammed.  After having a rough 2 months of GI issues, and cuting out most food (diary, meat, grease, carbonated beverages, and sugar). I finally am getting a Colonoscopy to see what in the world is going on! I'm been taking Probiotics, was on meds for both C. diff and AAD. I even added driking Kefir to add to the probiotics and good bacteria.  Only now am I seeing any changes, less stomach aches, etc. I add a 1/2 cup pf the Kefir to my smoothie, its not bad -yum! I really reccommend it and Probiotics (so talk to your doctor about it), it could really help you out! Read about Colonoscopies here! So I'm glad to be g...
4 comments
Read more

Um..Need to clear my head.

I was having a good day, it was one of my babysitting girl's bdays! We went for ice cream, I hung out with a friend and watched "Game of Thrones". I really liked it and I'm hoping to watch more this wknd. Then I logged onto Facebook to see that my best friend Laura (with CF) is down in lung function, on oxygen at night and her doctor is putting her on the Transplant list. I have lots of thoughts going through my head the MAIN one is "Please let her get a Tx soon, heal well and fast, and live her full life, they way she deserves to! PLEASE, PLEASE, PLEASE!" I can't imagine how she must feel, I know I'm sad knowing she is at point she needs one, but HAPPY she will get on the list! Happy, Sad, Scared, Excited. How do I feel..? The worst part is knowing that she is pain. I just want to take all that away, give her some good n plentys (one of our fave candy), kiss her on the forehead, tell her I love her, and that before she knows it she will have...
2 comments
Read more