Quick Context: CTV's Catherine Lathem has the story of parents' desperate plea to keep their little girl alive. Carter Roberts was diagnosed with acute flaccid myelitis cases -- or AFM -- two years ago.

Family Advocates For Research Into Rare Disorder That Claimed Infant Son -

CTV's Catherine Lathem has the story of parents' desperate plea to keep their little girl alive. Carter Roberts was diagnosed with acute flaccid myelitis cases -- or AFM -- two years ago. Patrick and Laura Sargent are members of a club no one joins by choice: The

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  • CTV's Catherine Lathem has the story of parents' desperate plea to keep their little girl alive.
  • Carter Roberts was diagnosed with acute flaccid myelitis cases -- or AFM -- two years ago.
  • Patrick and Laura Sargent are members of a club no one joins by choice: The

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Family advocates for research into rare disorder that claimed infant son

Family advocates for research into rare disorder that claimed infant son

Read more details and related context about Family advocates for research into rare disorder that claimed infant son.

Parents of baby with extremely rare disorder seek help for round-the-clock care

Parents of baby with extremely rare disorder seek help for round-the-clock care

CTV's Catherine Lathem has the story of parents' desperate plea to keep their little girl alive. Subscribe to CTV News to watch ...

Family Fighting for Research for Son’s Rare Genetic Disorder

Family Fighting for Research for Son’s Rare Genetic Disorder

Read more details and related context about Family Fighting for Research for Son’s Rare Genetic Disorder.

Kansas City parents become advocates for families dealing with rare diseases

Kansas City parents become advocates for families dealing with rare diseases

Patrick and Laura Sargent are members of a club no one joins by choice: The

Infant Who Survived Devastating Disorder May Go Home Soon

Infant Who Survived Devastating Disorder May Go Home Soon

Read more details and related context about Infant Who Survived Devastating Disorder May Go Home Soon.

Mother advocates for research after polio-like illness claims son's life

Mother advocates for research after polio-like illness claims son's life

Carter Roberts was diagnosed with acute flaccid myelitis cases -- or AFM -- two years ago. Her mother described the experience ...

Clovis baby battling rare genetic disorder, family fundraising for a cure 

Clovis baby battling rare genetic disorder, family fundraising for a cure 

Read more details and related context about Clovis baby battling rare genetic disorder, family fundraising for a cure .

Family Fights for Universal Screening for Son's Rare Disease

Family Fights for Universal Screening for Son's Rare Disease

Read more details and related context about Family Fights for Universal Screening for Son's Rare Disease.

Mother of child with rare disorder advocates for health care

Mother of child with rare disorder advocates for health care

Read more details and related context about Mother of child with rare disorder advocates for health care.

Family in Florida advocates for approval of medical treatment for a rare genetic disorder

Family in Florida advocates for approval of medical treatment for a rare genetic disorder

Read more details and related context about Family in Florida advocates for approval of medical treatment for a rare genetic disorder.