Parenting Children with MCS

The Chemical Sensitivity Podcast

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This episode is titled "Parenting Children with Multiple Chemical Sensitivity (MCS)."
It features an insightful conversation with a woman who has MCS and is the mother of two teenage daughters who also have the illness and Mast Cell Activation Syndrome (MCAS). My guest and her daughters live in Colorado in the U.S. and have chosen to remain anonymous to protect their privacy.

If you’re listening and have children with MCS, you may find my guest shares:

• Helpful information about the importance of listening to your intuition about children's chemical sensitivities or intolerances.
• That it's helpful to back up your thoughts with research.
• And above all, to trust yourself in advocating for your children.

I hope you enjoy the conversation and find it of benefit.
DISCLAIMER: THIS PODCAST AND WEBSITE DO NOT PROVIDE MEDICAL ADVICE
The information, including but not limited to, text, graphics, images, and other material contained on this website are for informational purposes only. No material on this site is intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health care provider with any questions you may have regarding a medical condition or treatment and before undertaking a new health care regimen, and never disregard professional medical advice or delay in seeking it because of something you have read on this website. No material or information provided by The Chemical Sensitivity Podcast, or its associated website is intended to be a substitute for professional medical advice, diagnosis, or treatment.

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Thank you very much to the Marilyn Brachman Hoffman Foundation for its generous support of the podcast.
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1. Parenting Children with MCS (00:00:00)

2. Guest talks about her shock when she first considered how she would help her daughter when she developed MCS. (00:00:05)

3. Aaron introduces the podcast and episode. (00:00:19)

4. Guest introduces herself and talks about her daughter. (00:02:56)

5. Guest talks about other illnesses her daughter has. (00:03:40)

6. Guest talks about when her daughter first developed MCS. (00:04:32)

7. Guest talks about how she adapted and responded to take care of her daughter. (00:05:40)

8. Guest talks about mould toxicity. (00:07:09)

9. Guest talks about how state officials did not believe her daughter has MCS. (00:09:55)

10. Guest talks about how she reads her daughter's body to understand her symptoms. (00:12:12)

11. Guest talks about how parents can understand how MCS affects their children. (00:13:56)

12. Guest talks about parents trusting their intuition about the illness. (00:16:07)

13. Aaron concludes the episode. (00:17:42)