Skip to main content

Doing All My Meds, say Wha?? :-)

On Track:

I've done all my meds since last Saturday! Wow, a full week!!! Which means I have finished my 5th FULL week! I'm participating in a CF fundraising Walk and my I promised everyone that for each $100 raised I will do a full week of meds! So far we have raised $645 (online) so I have another full week of skipping NOTHING to go! I will count cash/checks when they are turned in (either before or at walk).

I'm going to add that for every 5 new walkers registered I will do a full week as well! So join the walk and get four family or friends to join us too and I will do another full week!

We currently have 20 members, so anyone who joins starting now will be counted!

I know, I know, "you should do all your meds anyway..."  I try. But it is hard to stick to it. Late at night when I'm tired after play practice I want to just fall asleep. I don't want to stay up another hour to do meds. But knowing my family and friends have been actively getting people to join or raising money, reminds me how much everyone cares and reminding me why I do them in the first place!

Doing all my meds, man, I'm hoping to keep this up and stay on track!

I'd love to start jogging more. I haven't had much time. Now, I'm back to work, school, still in the play, and don't have a lot of spare time and when I do... I sleep. Sleep=good. Being back doing everything has been wearing me out a bit, but I LOVE being back and eventually I will get used to it!
And the play and school ends soon, so this summer I should have lots more time!

Very much looking forward to summer! And hoping my Clinic next month shows some increase in my numbers (since I'm doing sooo many meds, etc)!!! It should pay off! :-)

To join or donate to my Team (and help add another full week of meds) click HERE!!!
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