Saturday, February 28, 2009
Wednesday, February 25, 2009
Help this sweet family raise the funds needed to help adopt their sweet Baby O!
Visit In His Hands ~ Our Adoption Journey to enter Baby O's BIG Prize Package Drawing which includes a custom BbB doll!!!!!
Here is how YOU can win.... visit their website (link above) Donate securely using the ChipIn icon at the top of the blog. The suggested donation is $5, but you can donate any amount that you are led to give, as often as you'd like. For every $5 you donate, you will get 1 ticket in the drawing (so if you donate $15, you will receive 3 tickets, and so on). The more tickets you have, the bigger the chances are of YOU going home with one of the prize packages!
Soon after you donate using ChipIn, you will receive an e-mail (at the e-mail address you used while donating) from me that will include your ticket number(s).If you would prefer to donate without being entered into the Prize Drawing, simply let me know when you make your ChipIn donation. Thank you for your generosity!
GOOD LUCK EVERYONE!!
Tuesday, February 24, 2009
this was a quick picture with my phone right when we got our doll out of the mailbox, Hailey Grace LOVES it!!
Friday, February 20, 2009
Tuesday, February 17, 2009
Introducing the newest doll design here at Baby be Blessed!
Remember this little cutie from last year??
Well she finally made it off paper and into real baby doll life!
The only problem, is that she doesn't have a name!!
What should we call the newest addition to the Baby be Blessed family!
Leave a comment and let me know!
We will have a vote once we get some ideas!
Monday, February 9, 2009
Do you have a photo you would like to share on Too Cute...Tuesday?
Email them to firstname.lastname@example.org
HAVE A BLESSED DAY EVERYONE!
Friday, February 6, 2009
Tuesday, February 3, 2009
Monday, February 2, 2009
First I received an email from Janessa's Mom, which reads:
Well, Tuesday's the day. We head into clinic tomorrow morning (around 9) for Janessa to be prepared for her bone marrow procedure. They will put her "out" and then take a sample of what's going on in her bone marrow. The hope/goal is that the chemo she's endured over the past nine months has destroyed all the cancer cells and that she is truly in remission.If there are no cells, the next step will be to plan surgery for her port to be removed.She will be considered in remission if/when she remains cancer free for five years.So we will continue to go to clinic, but it will probably just be once a month.So, please be in prayer for her. She doesn't like to be put under and the sample is painful to the hip. Please pray for God's peace, comfort and protection for her during this procedure .....and most of all that the cancer is gone.We'll let you know when we know the results....Thanks Julie for all http://www.caringbridge.org/visit/janessaj
Second, here is an update on our sweet Carley from her Daddy Joel:
Hello Everyone, I am sorry that we haven't updated in a while but we have been on a roller coaster of emotions over the past week and have had to spend time processing all of the changes. Carley's tests did not come back as good as we would have hoped. Of course I already mentioned that her bone marrow is still dirty but the scans also revealed that she has stopped responding to the chemo treatments. Her newest set of scans showed that nothing had changed from the previous scans that were taken after her fifth round of chemo. Basically this means that her prognosis has gone from the good side of bad to the bad side of bad, humanly speaking of course. She is currently classified as having stable disease. The doctors at Riley have suggested that she be removed from her current therapy plan and that we look at other alternatives, which we are in the process of doing. The head of the stem cell department has put calls in to every neuroblastoma expert in the country. He has contacted individuals from Seattle to New York and is currently compiling a list of choices for us to make. At this point the most mentioned and most promising choice is a kind of radioactive MIBG therapy. Of course, like everything else in pediatric oncology, this therapy is only available as part of a clinical trial and there is currently only ONE spot left available on the current trial. This specific therapy was designed especially for children in Carley's situation. The only different approach that has been mentioned came from Sloan in New York and there recommendation is just to give her more chemo, we are reluctant to go down that path at this point because her cancer has obviously shown some resistance to chemotherapy. God is good and none of this has taken him by surprise. Percentages and human prognosis means nothing to him because ultimately this battle is of the spirit and not of the flesh. We understand the realities of Carley's situation but we also stand firm in our belief that when Man has little to offer, God is allowed to shine! Please pray that God would continue to work out all of the details and that we would soon be able to resume the type of therapy that he would have planned out for us. We hope to know something by Monday or Tuesday and we will let you know as soon as we can.
We lift these sweet girls up to you!
Please visit their Caringbridge site's to offer encouragement.
Let them know how many of us are praying for them!
Many Blessings to all of you!