If you are thinking of a gift to help us on our way,

A gift of cash towards our IVF journey will really make our day.

If you're insistent on a gift, please surprise us in your own way.

Hello Friends and Family!

It is with great pleasure to let everyone know that we were married in the presence of immediate family on 10.10.2020! We chose to have an intimate wedding in the mountains of Vail, CO mainly due to the unknown with health & travel concerns of all of our friends and family who would potentially make the trip.

As most of you know, Pete was born with a genetic disease called Cystic Fibrosis. CF is a progressive disease that causes complications within the lungs and digestive system, as well as potentially the reproductive system. While CF has impacted Pete’s daily life since he was a little boy, we learned several months ago that Pete is part of the 98% of males that will have complications with starting a family. That said, for us to be able to start a family, we were told we needed to undergo in-vitro fertilization (IVF). We are now well into our 2nd round of IVF with after an unsuccessful 1st round. While we are unsure with regards to what the future of the 2nd round of IVF has in store for us, we are incredibly optimistic. We hope that you understand why we have chosen this form of request rather than a typical gift/wedding registry for our big day.

If you would like to learn little more about Cystic Fibrosis you can do so by checking out CFF.org. Most friends and some family don’t know much about the impact of CF on Pete’s life, and there are thousands of young people out there who have, and are struggling with, more complications than Pete has had thus far in life.

From friends & family, acquaintances, giving strangers familiar with this journey, and unknown lovers of life, we appreciate any support you are able to give.

We truly envision this process not only brining joy to our collective lives, but also contributing to increasing awareness of CF on many different levels. To learn more about Cystic Fibrosis and how to give to the foundation, please visit https://www.cff.org/What-is-CF/About-Cystic-Fibrosis/. That said, if you would like to make a donation to the CF Foundation in lieu of a financial gift for our cause, we would be equally grateful.

Please also feel free to share our story and increase CF awareness by sending to your very own friends and family.

Love and Joy,

Pete & Crystal

843-813-0220 / 701-739-0467

3583 S Hillcrest Drive

Denver CO, 80237