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    At the Mito Foundation we strive for continuous improvement and want to ensure the online resources we provide continue to help improve the lives of people impacted by mitochondrial disease (mito). When we discuss 'you' or 'your' in this survey, we are including your child, family member, or friend living with or impacted by mito. By sharing your experience and answering the questions below, you contribute to shaping better resources for yourself and others. Thank you.

    Relating to the online resource you have just viewed, please rate the following:

    • 1. On a scale from 0 to 5 (where 0 is very poor knowledge, and 5 is all the knowledge you feel you need), how would you rate your knowledge?

    • Before you viewed the resource

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    • After you viewed the resource

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    • 2. On a scale from 0 to 5 (where 0 is very poor confidence and 5 is all the confidence you feel you need), how would you rate your confidence?

    • Before you viewed the resource

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    • After you contacted the Helpline

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    • 3. On a scale from 0 to 5 (where 0 is very poor wellbeing, and 5 is what you feel your wellbeing should be), how would you rate your wellbeing?

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    • 4. On a scale from 0 to 5 (where 0 is very poor access to the services you need, and 5 is you have access to the services you feel you need), how would you rate your access to services:

    • Before you viewed the resource

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    • Your understanding to access services you may need after you viewed the resource

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By submitting this form, you acknowledge and consent that your information will be collected, stored and used in accordance with Mito Foundation's privacy policy.