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This booklet provides important information for women with PKU and their support systems about managing the condition, particularly during pregnancy, through a special diet and face potential health
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How to fill out Women with PKU

01
Gather necessary medical documentation and history regarding PKU.
02
Complete any required forms accurately, including personal details and health status.
03
Provide details of dietary restrictions and needs specific to managing PKU.
04
Submit additional documentation from healthcare providers if requested.
05
Review all information for accuracy before final submission.

Who needs Women with PKU?

01
Women diagnosed with Phenylketonuria (PKU) who require tailored dietary management.
02
Healthcare providers working with patients affected by PKU.
03
Dietitians and nutritionists specializing in metabolic disorders.
04
Support groups and organizations focused on PKU awareness and education.
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Even women with less severe forms of PKU may place their unborn children at risk by not following the PKU diet. Babies born to women with high phenylalanine levels don't often inherit PKU . But a child can have serious problems if the level of phenylalanine is high in the mother's blood during pregnancy.
If not picked up at birth and treatment then started, PKU can cause severe mental disability. Normal milestones won't be reached, and the brain damage can be irreversible. Luckily, there is a treatment available; each child with PKU is followed by an amazing Metabolic Team and a diet-for-life begins.
Lillian Rodriguez is an actress in New York City. She also has PKU. Recently she began hosting a Twitter chat called #PKUChat. She spoke with advocate and filmmaker Kevin Alexander about #PKUChat and how people can participate.
Phenylketonuria (commonly known as PKU) is an inherited disorder that increases the levels of a substance called phenylalanine in the blood. Phenylalanine is a protein building block (an amino acid ) that is obtained from eating certain foods (such as meat, eggs, nuts, and milk) and in some artificial sweeteners.
A PKU mother can produce a healthy infant if she maintains a very restricted and controlled diet before and during pregnancy. However, even the most recent reports describe a very high incidence of congenitally abnormal children of PKU mothers, hence dietary compliance is not working in all cases.
My name is Kevin Alexander, and I live in Shreveport, LA. I am an adult living with PKU and since 2012 I've been an advocate for PKU, newborn screening, and rare disease awareness. I'm also a professional videographer, and in that time I have produced numerous videos raising awareness for our cause.

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Women with PKU refers to women who have phenylketonuria (PKU), a genetic disorder that affects how the body processes an amino acid called phenylalanine. This condition requires careful dietary management to prevent health complications.
Women with PKU are typically required to file to document their medical history and dietary management plans, especially those who are pregnant or planning to become pregnant, as they face specific health considerations related to the condition.
Filling out Women with PKU typically involves providing detailed information about the individual's PKU status, any dietary restrictions, medical history, and plans for managing the condition. It is advisable to consult healthcare professionals for guidance.
The purpose of Women with PKU is to ensure that women with the condition receive appropriate care, monitoring, and interventions to manage their health, particularly in relation to pregnancy and overall dietary management.
Information that must be reported includes the individual's PKU diagnosis, current dietary plan, medical history, any treatments being received, and future health plans, particularly regarding reproductive health.
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