Linda Franco Official: Instagram, Facebook | Linktree

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Linda Franco Official: Instagram, Facebook | Linktree

Linda Franco

Fundadora da Família ALD Brasil e mobilizadora social.

Aula sobre Adrenoleucodistrofia - ALD - com médicos neurologistas.

Sentimentos: segunda reportagem da série fala sobre coragem e resiliência

Instagram
 

Meio Dia Paraná - Curitiba | Junto de uma médica, mãe luta contra doença degenerativa que atinge filho | Globoplay

Portaria 199 - de doenças raras

II Simpósio Paranaense de Doenças Raras marca o Dia Estadual de Conscientização

Adrenoleucodistrofia - Doença abordada no Filme - O Óleo de Lorenzo

Instagram

Principais sintomas da Adrenoleucodistrofia

Sobre o café com as mães atípicas 2022 - Após perder filho por doença rara, mulher cria projeto para ajudar mães de crianças com necessidades específicas: 'A missão não acaba na morte'

Link do Programa - Como Será?

Sobre os grupos de doações entre as mães de crianças com deficiência.

Recebemos a visita dos caçadores de Bons Exemplos.

Sobre a nossa vivência e a nossa missão - Adrenoleucodistrofia.

Facebook

Sobre o Livro Mães Raras.

Grupo de Ação Social

Documentário/Site sobre a Adrenoleucodistrofia

Blog

Instagram

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About this account

lindafranco To help keep our community authentic, we're showing information about accounts on Linktree.

Joined April 2021

Linda Franco has been a member of Linktree for 5 years and joined in April 2021.

Resources lindafranco has populated their site with include:
• Aula sobre Adrenoleucodistrofia - ALD - com médicos neurologistas.
• Sentimentos: segunda reportagem da série fala sobre coragem e resiliência
• Instagram
• Meio Dia Paraná - Curitiba | Junto de uma médica, mãe luta contra doença degenerativa que atinge filho | Globoplay
• Portaria 199 - de doenças raras
• II Simpósio Paranaense de Doenças Raras marca o Dia Estadual de Conscientização
• Adrenoleucodistrofia - Doença abordada no Filme - O Óleo de Lorenzo
• Principais sintomas da Adrenoleucodistrofia
• Sobre o café com as mães atípicas 2022 - Após perder filho por doença rara, mulher cria projeto para ajudar mães de crianças com necessidades específicas: 'A missão não acaba na morte'
• Link do Programa - Como Será?
• Sobre os grupos de doações entre as mães de crianças com deficiência.
• Recebemos a visita dos caçadores de Bons Exemplos.
• Sobre a nossa vivência e a nossa missão - Adrenoleucodistrofia.
• Facebook
• Sobre o Livro Mães Raras.
• Grupo de Ação Social
• Documentário/Site sobre a Adrenoleucodistrofia
• Blog

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Linda Franco Official: Instagram, Facebook | Linktree

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