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07-03-2012, 06:33 PM
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#7 | |||
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My girls were 1 and 3 when I was dx. Ive never sheltered them from this. I had one more child, a son, after my dx. They have been raised knowing, and therefore knew from early on that mama cant always do the things I wanted or that they wanted me to do. IMO, its best they know young, but in their language, age appropriate is what I mean. Someone mentioned the books from NMSS and its a great idea. They give you alot of info on how to tell the wee ones. Its very helpful and free.
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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