A mother’s thoughts on having a daughter with disabling MCS
Life in the City with a Future
I asked my mom for the ultimate act of love this week. I asked her tell about her journey having a daughter who is disabled with MCS. Mom asked me for questions for her to answer. These are her words:
1. What did you first think when I told you I was disabled with MCS and you would have to eliminate all toxic chemicals from your life if you wanted to physically see me?
I thought, God. How do we do that — chemicals are everywhere? How bad is this going to get for my poor daughter? And of course, I thought about myself also. I have lived for so long doing everything using all kinds of awful stuff and not even paying attention until you get an awful wake up call and have to hope and pray it is not too late.
2. Two years after my disability from…
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What a lovely post..thank you for sharing Colleen’s post with your followers.
I love what Colleen is doing this week <3 My energy has been going elsewhere, and I haven't been able to focus on writing about it (although I will someday).
I've shared the original posts on fb and people there really love them so I thought my readers here who don't follow fb might also benefit from them :-)