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Maintaining Caregiving Services
I’m currently waiting for an appointment where I basically have to prove that I’m still very much disabled and still very much need caregiving services.
I know this is all par for the course if I want to continue receiving services, but I always get a little nervous that they’re going to take away some of my monthly hours. Sounds a little funny typing because nothing in my health has changed— or improved I should say. But I’m always afraid I’ll be a victim to budgetary cuts and federal changes.
Anyone else feel this way? Caregivers are the heart of my livelihood and the thought of losing hours terrifies me.
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3 Replies
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Oh my gracious, yes! No matter how many time we do it, it’s still a bit nerve wracking. Like said, there’s never any reason why it should change, but it still causes some anxiety.
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Sad but true. Especially when the ones making the rules have no clue.
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I’m so glad I’m not alone in this!
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