Living with MCS in Connecticut/New York?
My name is Miriam, I'm a college student and I'm trying to learn more about living with MCS. If anyone here lives in the CT/NY area or knows anyone who does and would be willing to talk about their experiences with me, I would really appreciate it.
If you'd be willing to talk with me, please let me know: email@example.com
Thank you all so much and best of health,
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