I figure there are two ways that a parent can let their kids in on the presence of a chronic health condition... Either we have a dramatic family meeting at some point (think Lifetime Original movie) where everyone sits down with serious faces and tries NOT to scare the kids (ultimately terrifying them, of course) or it can just be a part of our everyday lives from the beginning. I'd prefer that. I'm happy I was diagnosed when Emily was just a baby -- This will never be new to her or to Jacob.
My neurologist is urging me to go back on my disease-modifying therapy (Rebif) sooner rather than later. He's pushing for me to stop breastfeeding at 6 months so I can return to giving myself injections 3x / week. For obvious reasons, I'm not super motivated to do that! Thankfully I'm a dairy cow and have a full freezer of breast milk already (Moo). My symptoms have returned with a vengeance since Jacob was born and I doubt I'll be able to hide my Tin Man walk when I see the doctor this month. I still plan on arguing for at least another month or two, though.
Once I go back on Rebif I've decided I want to do my

 
 
You are amazing!
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