ONE IN A BILLION BABY! LITTLE GIRL BORN WITH ULTRA-RARE SYNDROMES NEVER SEEN IN ONE PATIENT STARTS MARATHON SURGERY LIST

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: In August Zoey had a surgery to attempt to fix her clefting but it since fell apart - she will need further extensive surgery, at least one a year until she is 18) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Megan with Zoey in hospital, the mum has Treacher Collin Syndrome, has daughter Zoey who is defying the odds to hit all her milestones despite being an unheard of case due to having so many problems in one child) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: In August Zoey had a surgery to attempt to fix her clefting but it since fell apart - she will need further extensive surgery, at least one a year until she is 18) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Megan who has Treacher Collin Syndrome, has daughter Zoey who is defying the odds to hit all her milestones despite being an unheard of case due to having so many problems in one child) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Mum Megan carrying little baby Zoey - Megan who has Treacher Collin Syndrome, has daughter Zoey who is defying the odds to hit all her milestones despite being an unheard of case due to having so many problems in one child) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Megan who has Treacher Collin Syndrome, has daughter Zoey who is defying the odds to hit all her milestones despite being an unheard of case due to having so many problems in one child) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Zoeys mum was told that no patient in records has the same collection of conditions that she does -she has The little girl inherited Treacher Collins Syndrome from mum Megan, the condition affects the development of bones and tissue in her face. But due to other chromosomal problems Zoeys condition manifested as a dominant form causing her bilateral cleft lip and palette, preventing her from feeding and forming words. She also has micrognathia, which stopped her jaw, chin and ear from developing correctly, as well as Pierre Robin Syndrome that contributes to the obstructions in her airways. She has an additional chromosome and a deleted one) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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captionPICS BY MEGAN TIDWELL / CATERS NEWS - (PICTURED: Megan who has Treacher Collin Syndrome, has daughter Zoey who is defying the odds to hit all her milestones despite being an unheard of case due to having so many problems in one child) - A little girl born with ultra-rare syndromes never seen in one patient starts her marathon surgery list to fix her face and help her to lead a normal life. Adorable Zoey Tidwell from Saucier in Mississippi, USA, battles an array of complications from undergrown facial bones, a large cleft, a smaller jaw and chin, difficulties breathing and more. Doctors recognised her issues during a 20-week ultrasound scan but after her birth pronounced she had one of the most severe bilateral clefts they had seen. She has no formed bones around her eye sockets and below, with even her jaw bones missing tiny chunks of bone. At only eight-months-old she is soon to have her second surgery attempting to fix her cleft, that will eventually allow her to eat without a g-tube and articulate words. Zoeys problems have been caused by genetic mutations leaving her with a deleted chromosome and an additional chromosome. Her case is so unusual that geneticists cannot find any other documented cases like hers and expect her to need surgery every six months until shes 18-years-old.- SEE CATERS COPY

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ONE IN A BILLION BABY! LITTLE GIRL BORN WITH ULTRA-RARE SYNDROMES NEVER SEEN IN ONE PATIENT STARTS MARATHON SURGERY LIST

01-12-2017

2017

Wacky People