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MS And Mental Health

UJ TeaWhen you are diagnosed with MS, there is no emotional support.  When you have had a relapse, there is nothing either.  You are told to ‘get on with it’ and similar phrases.

To which I say… ‘what?’

I was diagnosed at 23, which is young – I didn’t know who I was, where I wanted to be, or, at that point, what meaning I even attached to my life.

When I lost my legs, at 26, I went literally mental.  I ended up in mental hospital.

I now have yearly episodes of psychosis – and unsurprisingly the delusions always centre around my health.

I wasn’t able to cope with my illness and I wish I had had more support.  My health outcome would have been better.

Emotional support is necessary for people with MS.  Spread the word.

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