Skip to main content

Mail It In May! Let's Do It!

Mail It In May!


 May is here! Yay, it's getting warm out and May is also National Cystic Fibrosis Awareness, so please also check out my  May Day Post from 2013!

Many great things going on in May! I love being able to share about CF Awareness month, it's a great way to  promote fundraising! May 1st always brings back memories too though. Memories of my Grammer (Grandma Allicks). I spent a lot of my childhood with her, she was an amazing lady that loved painted toe nails, purses, beanie babies, and most of all her family! I wrote about why May Day always reminds me of her,

This week is Andrew's Birthday and lots of CF events! Starting with tonight in Champaign, I I have the pizza fundraiser my friend Alex is hosting. (He's in the pic on the right with Sarah and Stacey, they did the last Champaign walk with me!) Then tomorrow is the Champaign CF Walk. I still have a ways to go to reach my goal, thanks to those who have donated in person though!) Feel free to donate here : http://fightcf.cff.org/goto/ChampaignWalk.

I'm also the guest speaker at that Walk. Then I work a few days and my mom is then coming up to visit for a to few. She is going to Clinic with me, because I'm going to discuss a lot with Doc. This includes changing some meds and my wanting to get my stomach tube out!!! So yay! We'll see. Sooo much is happening this month! We have another walk in Naperville as well.

So what else could be going on in May?

 I've decided to use this month to kick off my "Mail it in May" fundraiser. I got this great idea from a friend who raises money for cancer every year! How it works is VERY SIMPLE. I understand some people don't like donating online, or let's be honest we get busy and forget. We don't have time to get our credit cards out, sit down, yadda yadda. I'm guilty of that sometimes. So instead I'll ask for people who are willing to send me donations in the mail! I'll send you an already STAMPED and ADDRESSED envelope and you just put your donation in it! Any amount, a couple dollars, $20, or whatever you want! If you want to send checks feel free. You can either write them out to me  or Cystic Fibrosis Foundation. If made to me, I'll put the amount into the walk site online page using my credit card ( so your check is accounted for right away). If you prefer CFF, then I will just hold on to the check until the walk and turn it in then, or sending cash is always okay too!

So whether you know me or not, are walking with us or not, live near or far away, you can still donate and help out! Let's see how much we can raise before  the walk using our good ol' snail mail system! All I need is you to message me your name and current address and I will send the return envelope right away!

So let's get this started! Let me know if you want to send a donation in the mail :-)

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

What Else Should I Do?

Need Some Feedback.       May has almost come to an end. I love May, nice weather, summer starts, AND its Cystic Fibrosis Awareness Month! A lot of the CF walks are in may and its a great time to raise funds and awareness for CF! However, I'm also excited that it will be June soon! June 28th is the Princeton Cystic Fibrosis Walk. I've helped organize other events in the past. Whether for school or other non-profits I've volunteered at, but this CF Walk is a little different. It is the first time, I've put together a City event. Or put together an event that is so near and dear to my heart. I'm so thankful that I had so many people sign up so quickly. Pretty much everyone family member I have on my mom's side signed up the first day. And I've have had some family and friends help me (giving me ideas, helping me recruit, etc). But, Its the first time I didn't have a committee or team behind me to help execute the ideas and actually plan the event. I lo...
2 comments
Read more