I am worried about, Sarah, of course.
About the other kids and how they are holding up.
That I will not have the mental strength to sit through a 2-3 hour MRI with Sarah today.
What the MRI might find.
I am worried that her neurologist will push for drugs like Avonex even harder if her MRI comes back with new lesions.
That if I tell him 'no thanks' once again to drugs such as these for Sarah that he will try and take my daughter away from me for being an unfit parent.
I am worried that things will never settle down for long enough for me to come up with a game plan for her and the care her father and I would like to give her.
I am more worried that she will lose her vision permanently, and that her world, as she puts it, will indeed go black.
I am worried that I will let this disease eat away at my soul, and make me a bitter person.
I am worried that I will start judging people even more than I do now - wondering why they can't/don't have a disease like MS, and Sarah does.
I am worried that Sarah will become bitter herself.
I am worried that I am not strong enough to be able to carry out family through this disease day in and day out for the rest of our lives.
I am worried that a cure will never be found.
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