My husband was diagnosed last year with CH by our GP and confirmed by a Neurologist.
We have started noticing since his last attack (+- 2 months ago), that his short term memory is not what it used to be.
I had to rush him to hospital for O2, who left him waiting for treatment for at least 45 minutes. We now have O2 at home.
I was just wondering if other people have noticed any side effects after an attack.