A diagnosis of FPIES can be life-altering. So, when The Mighty asked our community for some
of the things parents of children living with FPIES are doing, because of the
diagnosis, that other people may not realize, the response was incredible.
With over 150 million readers and thousands of contributors,
The Mighty has been building a community of online rare disease support. They “publish real stories by real people
facing real challenges”. They have
created a safe platform for rare disease community members and organizations to
connect with others, share their stories while raising awareness and support
for rare diseases as a whole. Together
we are strong.
The Mighty has given us the opportunity to share your
experiences in stories such as:
We are proud to be among the over 200 rare disease non-profit organizations that support and partner with The Mighty. We will continue to bring
additional awareness stories in the future.
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