Hello, I’m Alissa!
I have always had a passion for photography. Some might say my camera is permanently attached to my hand. In January 2013 I opened up Lissables Photography. I couldn’t be happier with the results. I am so thankful for all the support and love from my friends, family and clients.
The blog is a more personal project. I use creativity in all aspects of my life, and love to blog about it. I also blog my photography work, but it’s not strictly one or the other. I hope you enjoy it either way!
If you are reading this for Sawyers Craniosynostosis progress please feel free to ask me absolutely ANYTHING. No question is a silly question, and no question is out of bounds. There is no greater feeling than connecting with another Cranio family. You can email me at lissables@gmail.com
Hi Alissa
I followed your dad’s link here,
Something is up with you header images and Firefox. The page looks great in IE and Safari, but for some reason in Firefox they’re displaying behind the text rather than in front.
It’s likely a code glitch, because on the theme sample page over at wordpress eveything looks fine.
Mike
How do you find the time…lots of fun to follow:)
Kay I think you should have a section on your website where your fans can see your work, a photo section! Although I do love readying your writing I also LOVE flipping through all your pictures!! 😀
Cake is dumb.
Hi Alissa!
I’ve finally come around to going through your site! I love it!!!
Even though I check up on you all the time through fb, this is such a great website for you!
I hope everything is going well!
I can’t wait for you and Brandon to be parents! The nursery looks fabulous!
sending lots and lots of love
steph
Glad you had fun checking it out! We really cant wait to meet the little guy. I hope we are the good parents everyone thinks we’ll be! Haha Miss you tons. Hope your life is just as adventurous!
alyssa,
Your work is beautiful, and your pics are sooooooooooooooo entertaining!
Thanks for the inspiration
Wendy 🙂
OOOOOh… hurry up with the little man, we are all getting impatient! lol
Thank you for sharing your cranio journey. My daughter was diagnosed with metopic last month and will be haing CVR 8/21/13. Your story is an inspiration and I dont know how I will emotionally get through this but thank you for your blog!
Courtney Nichols