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My name is Laurine age 45 and new to this site. I have 4 children

ages 22,21,19, and 17. All show some signs of Mito. My oldest

daughter started having some problems when she was about 2 years

old. She is severly mentally retarded, has severe scoliosis, and was

followed by Shriners since she was 8-18 years old. It was Shriners

who did a muscle biopsy and found abnormal mitochondrial but they did

not know what to do with this information so it was put on the back

burner. I had thought about not having anymore children after she was

born, but I was already 2 months pregnant with my second daughter. My

second child was said to be perfectly normal and my first daughter's

problem was probably not genetic. So I went on to have 2 more

children, both boys. My youngest was 6 months old when he had a near

SIDS. He is a junior in highschool today. When my oldest turned 18

she started having siezures and docs also discovered mitral valve

prolapse. I at this time was thought to have MS. I had a fresh

biopsy done in June 2004 resulting in a diagnosis of Complex I and

III. I had the biopsy done because my oldest daughter would not

survive a surgery. After the biopsy results it became very clear

what was happening in my family. My grandmother, and her sisters, my

mother and her sisters, my sister, myself, and my kids all have

symptoms of this horrible but terribly interesting disorder. Oh by

the way I am a nurse and it is all very interesting from a nurses

point of view. I have been researching this since 1999. You all

have been so helpful and I admire your courage and faith. Prayers

are with you always.

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