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 :-)

Comments

Popular posts from this blog

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

Post- Surgery Appointment

Post Surgery Appt: As you prolly know, I had Laparoscopic Triple Hernia Surgery last Tuesday. Here was a picture of me devouring a piece of bread so I could go home afterward the surgery (4 hours post surgery and 20 mins post waking up from recovery). I was ready to go home! Today I had my post surgery check up. He said everything in the surgery went well and besides the finding the 3rd hernia there were no surprises. He pointed out where the staples/stitches (they are holding the mesh in place) are in me. I have two on each side at the end of the mesh (so 4 on top) and two down farther in my groin. Apparently, I just have one huge piece of mesh that runs the width and length of my whole abdomen/groin area. Bahaha. I am Inspector Gadget after all. He said a few more weeks before I can lift stuff or exercise. Also, he said the area where the staples are will hurt when bending or twisting. However, I only notice really when I twist or turn too fast. Overall, it was a nice appointment

Big Update Time & what I need!

Time Flies: I've been blogging about all these separate things I have going on in my life. My lung function drop, the hospital stay, my stomach/ GI issues, the surgery, the Princeton IL CF walk, my fight with insurance for my Cayston medication/machine, and soooo much more. So here's a bit of a catch up for everyone! Let me start at the very beginning: read my CF history in this brief post here . Now let's skip ahead to the last 6 months. From September 2014 - Feb 2015 I lost 3 CF friends ( it was really tough). In September my best friend with CF (from childhood & on) passed away from CF. I wrote a post about her journey, love for life, and how she was (& is) my inspiration to fund raise (read about Laura's Journey here ). Then in October I got my G-tube taken out/ fistula fixed and removed. YAY YAY YAY! The abdominal surgery was my 15th surgery, so I recovered pretty quickly. I'm beyond thrilled to say after 15 YEARS with a G-tube and needing to u