10 things I know about MS as a caregiver

  1. Your friends stop coming around.
  2. Finding help to get things done is next to impossible
  3. The MS Society will give you token help and then disappear
  4. Once you find a good neurologist, you hang on to them
  5. Your friends stop calling
  6. Each day is a lesson in frustration and anger
  7. It is possible to both hate and love someone at the same time
  8. Being a caregiver is exhausting
  9. Staying sane is a tightrope walk
  10. Very few people hear your pleas for help
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About doggonedmysteries

Agented Mystery Writer, Bull Terrier owner --we have two, Avid gardener.

Posted on March 14, 2016, in MS related and tagged , , , , , , , , . Bookmark the permalink. 1 Comment.

  1. I hear you. I sympathise. I wish I could help. Your words do not fall on deaf ears.

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