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Too Much – LET’S CHAT
I am NOT a doctor but I have been living with MCAS for decades (before even knowing what it was). Always wish, I could get support (a little talk therapy) during all this trial and error. Even once I found a doctor (which I love, love, love) I still found it hard to talk through things as appointments can be months or even a year away. 🙂

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Mel Robbins – Let Them – Let Me – Chronic Illness
Online MCAS Communities
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MCAS and LDN (low-dose naltrexone)
MCAS and Migraines: Understanding the Connection and Managing the Pain

Hydration Drops.

Check It Out!
This is what I use -FYI – I will if you click from here get a little residual and you should get 20% off but check out the chronic illness option.

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Mast Cell Activation Syndrome is hard to understand – as a community, let’s put the pieces of the puzzle together.

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