the rare village


where families with rare conditions will help each other navigate the unknown



This isn't live yet. We'll only build it if enough families want it.
are you in?

You are not alone in feeling alone

We have all been there.
The fear.
The loneliness.
The endless unknowns.
But we don't have to do it alone anymore!
This is our village. A place where we share what we’ve learned, so no one has to start from zero. If it can help even one person feel less alone, our village has succeededYes, each of our children is unique, and these conditions are ranges. But the more information we share, the clearer the picture becomes:
- What to look out for
- What to fear (and what not to)
- What has helped others
By ourselves, we're alone. Together, we can get through anything.


Why current options fall short

When your child is diagnosed with a rare condition, doctors often can't answer your most important questions: When will they hit milestones? What medical issues should you watch for? What will the future look like?You eventually find a Facebook group, but information is scattered, hard to search, and new families ask the same questions over and over.And if you don't use Facebook? You might never find your community at all.


A Searchable Database of Real Experiences

The Rare Village is a platform where families anonymously complete questionnaires about their experiences. We aggregate the responses by diagnosis so you can see:✓ What percentage of kids hit milestones at different ages
✓ How common specific medical issues are
✓ Which therapies families found most helpful
✓ The real range of outcomes- not just one story
Think: crowdsourced data, not a forum.


For families, by families

📊 See the Range
Not just one story - see experiences from 10, 20, 50+ families with the same condition
🔍 Actually Searchable
Find what you need without scrolling through years of Facebook posts
🔒 Your Privacy Protected
Anonymous sharing. No data sold to pharmaceutical companies. Ever.


This is for you if...

👋 You just got the diagnosis and feel completely alone.
👋 You're wondering "is this normal?" and can't find answers anywhere.
👋You want to see the full picture- not just one story, but the range of what's possible.
👋You remember how terrifying the early days were and want to help the next family.
👋You're tired of Googling at 2am and finding nothing useful.
👋You're looking for your village.


Imagine if..

The day you got your child's diagnosis, you could search their specific condition and see:
- 47 families have shared their experiences
- Most kids walked between 18-36 months
- 12 families had the same scary symptom - all turned out fine
- Physical therapy started early made the biggest difference
That's what we're building.


be a part of this vision

This only works if we're in it together.
We need enough families who are not just interested in using it, but willing to share their own experiences to make this database meaningful.
Sign up to show there's demand.
Let's help each other and be the help we wish we had when we had started out on our journeys!


Are you in?

Because it really does take a village.


Questions? comments?

Reach out at [email protected]

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