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** For those of you who are looking for Stem Cell Advise**

Since Konnor's new diagnosis I don't feel that I am a very good source of information regarding Stem Cell Treatment & CP.  Although, I can point you in a good direction to get in touch with more parents who have done SCT w/their children with CP.  It is an online group called BIA4kids (Brain injury alternatives 4 kids), you can join by going to yahoo.com, groups and request to be a member of BIA4Kids.  It is full of parents who do alternative therapies for their brian injured children.  Even looking through old posts with give you alot of information and list results that other parents have noticed in their children after receiving SCT.*** 

 
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From Stan Carr

September 01, 2010

Wonderful website Lisa. I particularly enjoyed your reminiscence of going to Holland instead of Italy. You are a good Mom, and Ken is a good Father. You guys seem to make Holland work just fine. I love you, Stan

From Carolyn Swantek

August 26, 2010

Thank you, just reading you site has helped us, my 4yr. old grandsom Malaki was diagnosed with CP, and just 2 weeks ago after much prayers and worry his father decided to have a Rhysatomy. Malakis headaches were the worst. he cried for days if anyone moved him, even gave him meds is his tube. We are still waiting to see any good results, he is going back to PT 4 & 5 days a week now. Pray for Malaki..

From Grampa Boles

August 20, 2010

I woke up one morning after a storm, a long way from home. Lightning raced all night long. I laid thinking what the day would have in store for me. I thought about the day before,all the anticipation of where I was going. The smell of sage drifted through the air. The sound of that early morning bass fisherman headed for the perfect spot. The first sound of the birds awakening. Was put to peace with the sound of "Granpa are you there" comming from the tent next to me. My journey was complete.

From stephanie Kuiper

August 04, 2010

I love you Konnor! You stole my heart the first time we met. You are by far the strongest and happiest person I have ever known. I keep you in my prayers forever!

From kimberly Mahurin

July 17, 2010

Your site is great!! Great that you want to being awarness. Your story where you talk about not knowing what his condition meant, but you know its bad reminded me of when Tristan was diagnosed and how I felt. Very scary. But god has been blessing us every day!!:-)

From Carol Petersen

July 17, 2010

Hi Lisa, Ken & Connor, It's great to hear that Connor has started kindergarten. You are in my thoughts and prayers. God Bless PS. I am hosting the "Stem Cell Awareness Seminar" on August 28th @ Marriott Tampa Airport Hotel.

From Jeannie West

July 17, 2010

I didn't know about your website before, but it's wonderful. It's great to learn so much information and what is going on. I love you guys and am thinking of you.

From konnor daniel boles

January 18, 2010

good job momma! i love you.

From Keith Theobald

January 01, 2010

Hi from the east. This is Keith and Stefanie. Enjoy getting your updates and just wanted to say Happy New Year. Sounds like you guys stay busy. Connor looks good and like he enjoys life. I love to see his smile. Keith is doing about the same no improvement after China. He thought about going back has no plans as of now. Take care of each other. Stefanie and Kieth

From Stephanie

December 19, 2009

I have read your blog on your son Konnor and it brought me to tears. My son who is 18 mo now has been diagnosed with cp since he was 6 mo old. My heart feels for you and knows what a struggle it is to raise a child with special needs. You never expect something like this to happen you just think your going to have a normal child and everything will be perfect. I have spent many a night crying wondering why this has happened and why God would do this, however in recent months I have come to understand the gift my son has given to me. The gift to reach out and do something meaningful in my life and for other children who have special needs. I just want you to know my prayers and thoughts are with you and your family and hope that Konnor will receive the best care he can get in hopes of any improvement for his future life. I also want to tell you that your website is a wonderful gift for other parents. Best wishes, Stephanie