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They pushed him to not go to school, to never work and frankly, to just stay home and do nothing.Since my husband is RRMS, he had full use of his legs and despite tremors in his left arm, if you were to look at him, you would never know he had MS.Then you’re instructed to put on your own oxygen mask first before assisting your fellow passengers.Hearing that simple directive always gives me a guilt twinge — I’m a caregiver at heart — even though I understand the reasoning behind it.
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I think one of the best places to start reading this blog is the article, Finding Caregiver Support I know exactly how you are feeling.
My husband was diagnosed when he was 18 and received very little support from his parents.
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His whole focus is working part-time and even though he chooses to goof off with other co-workers which has caused problems.