Abigail Renee Kasuba
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WELCOME
Our Dear Abby passed away March 10, 2009. We have decided to leave this website unchanged, but have added one new page, the "Last Page". Please check it out. It is in memory of Abby and tells the last part of her life with us. Abby's life will never leave our memories, so as times goes by, it is only sensible there will be new stories added to this website.
We are no longer in need of donations.
We encourage you to continue to look at this website and pass it along to others to remember Abby's
beautiful presence in this world and create awareness of mitochondrial disease. Now more than ever we need people to become aware. The reality is, once given this diagnosis, too often it is a death sentence for so many children.
Please always keep memories of Abby.
See our guestbook to write something if you like!
Our Dear Abby passed away March 10, 2009. We have decided to leave this website unchanged, but have added one new page, the "Last Page". Please check it out. It is in memory of Abby and tells the last part of her life with us. Abby's life will never leave our memories, so as times goes by, it is only sensible there will be new stories added to this website.
We are no longer in need of donations.
We encourage you to continue to look at this website and pass it along to others to remember Abby's
beautiful presence in this world and create awareness of mitochondrial disease. Now more than ever we need people to become aware. The reality is, once given this diagnosis, too often it is a death sentence for so many children.
Please always keep memories of Abby.
See our guestbook to write something if you like!
We are striving to raise awareness of mitochondrial disease, share Abby's and our family's story, and hope to receive help in order to better Abby's quality of life.
Thank you for visiting Abby's site.
Tom and Beth Kasuba
Thank you for visiting Abby's site.
Tom and Beth Kasuba
Abby at 1 year of age.
Abby now, at 8 years old.
Abby was an energetic girl with a spunky personality. She was very affectionate, strong-willed, had a sweet smile, was polite, loved music and singing along with songs and played well with her brother. I miss Abby's laughter, smile, and voice. Sometimes I almost forget how her voice sounded. I miss everything about her that she has lost, but still love her dearly for who she is today. I believe if we had not had this experience with Abby I would be a different person; more shallow and taking every day for granted. That is no more. Every hour with her is so important, as it also is with Timmy. Creating this website has been very difficult and sad for me. Thank you for your time to read about Abby, learn more about mitochondrial disease, and support us.
Beth
Beth
Hi! My name is Abigail Renee Kasuba. Everyone calls me Abby. Welcome to my web site. My Mom and Dad have created this for me and in honor of me. I have mitochondrial disease. I hope you will take the time to read my story and browse the site. Check out my photo page. I hope you will come back often for updates.
Love, Abby
Love, Abby
Abigail Renee Kasuba
April 16, 2000
6 pounds, 15 ounces and 19 inches
