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Контент предоставлен Raising Rare. Весь контент подкастов, включая эпизоды, графику и описания подкастов, загружается и предоставляется непосредственно компанией Raising Rare или ее партнером по платформе подкастов. Если вы считаете, что кто-то использует вашу работу, защищенную авторским правом, без вашего разрешения, вы можете выполнить процедуру, описанную здесь https://ru.player.fm/legal.
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Manage episode 324399525 series 3294266
Контент предоставлен Raising Rare. Весь контент подкастов, включая эпизоды, графику и описания подкастов, загружается и предоставляется непосредственно компанией Raising Rare или ее партнером по платформе подкастов. Если вы считаете, что кто-то использует вашу работу, защищенную авторским правом, без вашего разрешения, вы можете выполнить процедуру, описанную здесь https://ru.player.fm/legal.

Have you ever been listening to a podcast and wish you could suggest a question for the interviewer to ask? You know there is something else you want to know but the conversation just seems to miss it.

We have and we wanted to try something new to address the issue. Recently, Sanath put out a request to ask him anything with the promise we would answer as many as we could on our show. It was a bit scary, not knowing what we might have signed up for. But a commitment is a commitment.

In this episode Sanath address a few of those questions.

  • How to give it your all to help your child with an ultra-rare condition when you don’t know where to start?
  • Any treatment for kids with Sanfilippo Syndrome? Can I get access to clinical trials? https://curesanfilippofoundation.org/what-is-sanfilippo/
  • Parenting I so hard but parenting a rare disease child is even harder. What can the community do to help? How do you manage emotional and mental toll that comes with raising a rare disease child?

These questions gave us a chance to talk about other important issues like risk, access, and the inherent issue of our healthcare and support systems.

If you like the “Ask Me Anything” format, watch for future requests for questions.

  continue reading

89 эпизодов

Artwork

Ask Me Anything

Raising Rare

published

iconПоделиться
 
Manage episode 324399525 series 3294266
Контент предоставлен Raising Rare. Весь контент подкастов, включая эпизоды, графику и описания подкастов, загружается и предоставляется непосредственно компанией Raising Rare или ее партнером по платформе подкастов. Если вы считаете, что кто-то использует вашу работу, защищенную авторским правом, без вашего разрешения, вы можете выполнить процедуру, описанную здесь https://ru.player.fm/legal.

Have you ever been listening to a podcast and wish you could suggest a question for the interviewer to ask? You know there is something else you want to know but the conversation just seems to miss it.

We have and we wanted to try something new to address the issue. Recently, Sanath put out a request to ask him anything with the promise we would answer as many as we could on our show. It was a bit scary, not knowing what we might have signed up for. But a commitment is a commitment.

In this episode Sanath address a few of those questions.

  • How to give it your all to help your child with an ultra-rare condition when you don’t know where to start?
  • Any treatment for kids with Sanfilippo Syndrome? Can I get access to clinical trials? https://curesanfilippofoundation.org/what-is-sanfilippo/
  • Parenting I so hard but parenting a rare disease child is even harder. What can the community do to help? How do you manage emotional and mental toll that comes with raising a rare disease child?

These questions gave us a chance to talk about other important issues like risk, access, and the inherent issue of our healthcare and support systems.

If you like the “Ask Me Anything” format, watch for future requests for questions.

  continue reading

89 эпизодов

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