Emily had a heart of gold and as her parents we are doing something for her; we had these made:



They come in two colors Pink and Purple (non-latex). But currently we are out of the pink ones.

They read on them

Emily Elizabeth Brammer Foundation
Children of falling TV & Furniture Awareness

We are trying to get new bracelets ready for next year.

They will be reading:

Children of falling TV & Furniture Awareness

I  hope to put Emily's name and 4 other names of children that have died from this cause. I wish I could put more names on them but I am only allowed 4.

If you are one of these parents  and want your child's name on the band. Please email us. So we can get the fine print to printer and get them ready for the next year.

I am also considering the color orange for caution.

My mommy and daddy want to get the word out.
A loss of a child never goes away.


Please email
 emilyelizabethbrammerfoundation@yahoo.com

We are more than willing to talk to you.

Emily Elizabeth Brammer Foundation

2529 Jewett Road

Burleson, TX 76028

817-426-3550

We are working on a blanket for children killed by TV and Furniture. We are hoping that other parents will come and join us and add their child's name to this blanket. each blanket part for each child will be made by their family. So they can tell the child's story and we will link the blanket together as one. This is still a work in progress and I am thinking of ways to have a big celebration of life for these children. I would like this to help everyone understand the dangers and precautions one needs to take in their home, these things happen in seconds and can't be taken back. Contact me if you would like to take part in this project and help me plan more of it.

Legacy
of 
Emily Elizabeth Brammer
By
Mommy and Daddy
Robert & Julia Brammer



Legacy is to some people is something that is left to them by someone how has left this world. Well for us it is different.

I want you to know what Emily Elizabeth Brammer went through to get here on earth, and I want you know that she was a gift of life to all of s on earth that is left behide. So take a site and listen to the wonderful story of her life.



Hello we are the proud parent of Emily Elizabeth Brammer. We wer so lucky to have wonderful daughter. She will be in our hearts forever. Emily light will grow cause, We are taken the stand to ssave lives of children through out the world. Please take the time and get to know our wonderful little angel.



Emily Elizabeth Brammer cam in this world on 

September 10, 2004. She had fight for life from the start. Born at 29 weeks and fight began. She was so tiny and small. Hot day in September, she was 3lbs. 5oz. and 21 inch long. I don't remember it so well. I was so sick too. They decide she would better off out then in. Robert being by my side going through everything. She cam into this world. He was so over whelm by joy of her. Now our life as a family was to start. But Emily at NICU at Cook's Children Hospital and I at Harris Hospital in ICU. In which I stayed there for four day's. I remember waken up and asking him. What does she look like? He said just like you. I wanted to know what she looked like so bad. But being in ICU, I didn't get to see her just yet. Robert got a picture of her. I have to say she was so pretty. They ran test after test on me. But couldn't find nothing, or why this all happen. I ended up staying at Harris Hospital for eight days total. But when they put me in my room final. Robert needed to go and get my bag from the car. Not knowing about hospital's and all. He got lost and got up set in the ER cause the officer there. Told him if he could not use a softer voice to leave. I have to say I was up set and told my nurse to come and let me go home. I didn't need this on me after what I have been thur. I have to say that officer has no heart. I final got to go over late at night. She was just like a princess. Her room at home had pooh in it but that was not her. She was our little princess. So everything we found in princess's she had it. So not coming home right away gave us time to do a few things before she got home. Robert was getting things ready at home for her. I just didn't have the heart to leave her there at the hospital. 


Well the tiny thing in my arms is Emily. My heart was so full of joy and happiness. But then doctor's talked to us. They saidn some babies do just fine and some don't. But they say girls seem to fight more then boy's do. In the NICU at Cook's Children Hospital, we meet alot of people in passing. I think one family we ended up being good friends is Galinak. Their son was just born 8 day's after Emily. We talked in passing and waitting our turn with our child. There were a few others as well. I think as mommy's we looked out for each other there. I think Emily stay was ok not the best for us. But we had bad nurse's at time's.  I just sometimes with the job it self gets to them. But to me they can't have time for that in this job at NICU. I remember start off in one place and then moving to another. Room by her self. I remember her be moved again and again. So many time it seems you start off again from the first place she was. I can remember one day visiting and finding a red area on her chest. I asked the nurse if I could talk to the doctor. I asked him what that was? He told us it is nothing to worry about. But that area got bigger. So I told the nurse again can you get the doctor. I asked again what is that red area on her chest. So they used a pen on that area. They ran test on her. She had so many IV's in head~hands~arms~feets~ they just seem to stop working after she has so many. They decide put a central line in her, they said she needed one~ they tried her chest area and couldn't get it. Then they got it in her right leg. But the sad thing was she still go IV's. We didn't understand that one. But she ended up with staff infection twice. They thought it was my breast milk. That come back not to be true.