TPIRC

This is the final week.

All month we have been sharing what food allergy families carry every single day. The fear. The survival mode. The emotional weight that no system has ever been built to address.

4 days left for this campaign.

Help us build what should have existed all along. Link in bio to support.

There is no standardized system of care for food allergy families carrying the emotional weight of this disease. Our team knows it. This is what they have to say about it.

5 days left in May. This is the final push.

Treating the physical burden is only half the picture. As bodies find freedom, the fear, the anxiety, the years of survival mode, those need support too. No integrated system has ever been built to do that.

Help us finish strong.
Link in bio to learn more.

There is a moment every food allergy family knows.

The Epi-pen is in the bag. The action plan is on file. The physical side is being managed. And yet the fear hasn’t gone anywhere.

So you look for help. You search for someone who understands what it actually feels like to live with a life-or-death allergy. Someone who gets the hypervigilance, the sleepless nights, the panic that doesn’t turn off even when everyone else has moved on.

Here is what you find. Out of pocket costs just to get an initial evaluation. A therapist who has never heard of anaphylaxis. No connection back to your allergist. No standardized protocol. No one tracking whether you are actually getting better.

You are left to bridge that gap completely alone.

That is the current mental health system for food allergy families. And it has existed for too long.

We are building the alternative. The first end-to-end clinical model designed specifically for food allergy families. Insurance covered. Specialists trained in food allergy distress. A consistent standard of diagnosis and treatment integrated directly into the care journey.

Help us replace a broken system with one that finally works for families like yours. Donate at the link below. 💙