I love make friends so if you have facebook you can add me!! I will be very happy to talk with you !!

My site is the journey from birth to now, related to my cleft lip, cleft palate, my teeth, and my fistula. I'm campaigning for donations to help acheive my goal of a healthy mouth, teeth, and smile, which will allow me to live pain free and have a much improved quality of life. I'm also hoping it will serve as a guide to parents of clefts, so that they may be able to prevent their children from facing the same obstacles I have endured.

My site is mostly in relation to anyone interested in a home busines. Unfortunately I can not advertise the company due to copyright, but what I can tell you is that the products are NON-TOXIC, Environmentally safe that you would use everyday within your home.
I actually found this company by accident I was not looking for a home business I was more interested in the products that the company has to offer. Being a mum of a cleft affected baby and wanting to eliminate as many chemicals I use in my home this company is just amazing. Want to know any information I can certainly give you a call and tell you more about the products.

This is my blog about our family. I am a single mom to Katie, age 4, and Sarah, age 2. Katie was born in Kazakhstan and I adopted her in 2004. Sarah was born in China and I adopted her this year. Sarah has a bilateral cleft lip and palate. Her lip was repaired in China and her palate surgery will be done here.

This is where I blog about my pregnancy and Alice's arrival (with unilateral cleft lip and palate) and progress. Also includes various thoughts about writing and my 'career' as a poet, or lack of it...

Rachel was born August 31, 2004, with a unilateral cleft lip, palate, and aveolar ridge. I created this blog shortly after her birth to keep family, friends, and others to see and follow her progress in the journey to getting her clefts repaired.

Not only has it been a place of keeping others up to date on Rachel and her journey, it's become sort of an online scrapbook and journal of day to day happenings now that this stretch of the journey has slowed down a bit. To avoid all the posts of the day to day happenings, I have created categories, listed on the left side of the blog that take you directly to the cleft related stuff. I hope that the information and pictures and the sharing of Rachel's Journey will help others and be a source of encouragement to those who are also dealing with a child having been born with a cleft of some sort.