I'm a newbie in this world of parenting a “medically fragile” child. I have found that almost a year in I still have a truck load full of questions. For other moms who have been in this world a while, I'd love your hard-won insight. Comment below or email me: stephanielanier@gmail.com
Does the grieving end?
How do you help other people understand your child without making excuses for them?
How do you deal with the medical bills, insurance, coverage limits, disability claims, medication administration, the doctor's appointments, marital stress, IEPs, etc. Do you really adjust to the amount of work that is involved in caring for your child?
When and how did you make the decision about having more children?
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