Lorrie, I didn't know the story behind Peyton. What a heart touching story. You and your family are close in thought. I will be honored to attend any fundraiser. I will check Peyton website for updated information. God Bless.

mike and lorri i will keep all of you in my prayers and you can count on me to help in any way i can. i will try to organized a fundraiser here for her.. god bless you all and what wonderful advocates Peyton has on her side... give my love to both the girls and know that you are amazing parents and miracles happen everyday . Love to all, barbie

What a beautiful girl who is lucky to have such strong and loving parents. Lorri, I had no idea of what had happened. Now that I have this information, I will share it with all my friends and family, as well as our large church. Please let me know when you have another fundraiser. We will keep you all in our prayers!

Peyton's EEG was moved to Jan. 4, 2010. We came home this afternoon. Peyton was monitored for 51 hours. The doctor was able to observe the changes in her brain while having seizures. He was also able to tell us where the seizures were occurring. Peyton had 5 seizures during the 51 hrs. We have a follow up appointment with her Neurologist on Monday Jan. 11, 2010. At this point, the doctor stated that Peyton's greatest chance for reducing the seizures is by medication. So... our goal is to completely stop any seizure activity and by this we will have to use alternative treatments. We are planning on resuming Hyperbaric Oxygen Therapy in February. She has responded well to this form of treatment in the past. Unfortunately, the benefits are not permanent. On a good note, the seizures Peyton did have while being monitored were very mild. The intensity and duration have greatly reduced in the last few months. The Stem Cell Treatments would be the reason for the change in seizures. Thanks again for keeping Peyton in your thoughts & prayers. I would also like to thank those who continue to donate to Peyton. Thank You!!!

Hi - I have been thinking of little Peyton recently and decided to check how she is doing. I don't know if you have time to answer, but I wondered if she is still getting HBOT treatments and if they proved successful in the long run. Many thoughts and good wishes remain with her and her wonderful family.