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

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.

Leave a Reply

Fill in your details below or click an icon to log in:

WordPress.com Logo

You are commenting using your WordPress.com account. Log Out / Change )

Twitter picture

You are commenting using your Twitter account. Log Out / Change )

Facebook photo

You are commenting using your Facebook account. Log Out / Change )

Google+ photo

You are commenting using your Google+ account. Log Out / Change )

Connecting to %s

%d bloggers like this: