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Nutrition Equity Episode 12: HCU Awareness Month Cobalamin G Heather Parent

October 25, 2023 Joanna
Nutrition Equity Episode 12: HCU Awareness Month Cobalamin G Heather Parent
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Nutrition Equity Episode 12: HCU Awareness Month Cobalamin G Heather Parent
Oct 25, 2023
Joanna

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In this episode I talk with Heather a parent of a child with Cobalamin G.  Cobalmin disorders are named for the order in which they were discovered.  Some Cobalmin disorders fall under the Homocystinuria Family, some are Methyl Malonic acidemia's and some are both.  They are tested for on Newborn screening, but often missed.  Heather's child Kodi is one of the children who almost lost his life to Cobalamin G.  Kodi suffers from Seizures and Cerebral Palzy as a result of late diagnosis and he is also tube fed through a feeding tube that is surgically inserted into his stomach.  Thanks to a medical student he lives today.  He is can say a couple words, and he signs, but for the most part at 3 years old he is non-verbal.    If you would like to help us fight for the Medical Nutrition Equity act please visit nutritionequity.org.  On the website you can read patient stories, see state by state coverage, write your senate and house reps and much more.  Please consider subscribing to this podcast and writing a review.  You can also support the effort by donating to it, anything you are willing to give could greatly help the cause.  Thanks you for listening. https://www.buzzsprout.com/2204433/monetization/supporter_settings

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Send us a Text Message.

In this episode I talk with Heather a parent of a child with Cobalamin G.  Cobalmin disorders are named for the order in which they were discovered.  Some Cobalmin disorders fall under the Homocystinuria Family, some are Methyl Malonic acidemia's and some are both.  They are tested for on Newborn screening, but often missed.  Heather's child Kodi is one of the children who almost lost his life to Cobalamin G.  Kodi suffers from Seizures and Cerebral Palzy as a result of late diagnosis and he is also tube fed through a feeding tube that is surgically inserted into his stomach.  Thanks to a medical student he lives today.  He is can say a couple words, and he signs, but for the most part at 3 years old he is non-verbal.    If you would like to help us fight for the Medical Nutrition Equity act please visit nutritionequity.org.  On the website you can read patient stories, see state by state coverage, write your senate and house reps and much more.  Please consider subscribing to this podcast and writing a review.  You can also support the effort by donating to it, anything you are willing to give could greatly help the cause.  Thanks you for listening. https://www.buzzsprout.com/2204433/monetization/supporter_settings

Support the Show.

childs diagnosis story
deer story fed but not nourished
20 step schedule (brain)
Symptoms
Physical and Occupational Therapy
ER Visit
Cody responds
Medical student hero
teaching hospital like to solve problems
daily struggles
others don'r understand
popularity with fire fighters
hope
vitamins are covered by the MNEA
Favorite foods
favorite foods Cobalamin patients don't follow a low protein diet
Cobalamin disorders are often missed on Newborn Screening
Full panel genetic testing is required in most cases for diagnosis
How the MNEA would help
advocating
personal stories
awareness and support
how lawmakers, doctors, and the general public can empathize
resources
hopes and aspiraspirations for the future
advice to newly diagnosed