My cousin is 44 and has a severe learning disability as well as cerebral palsy and epilepsy. She went into residential care over a year ago and was recently moved to a new bungalow where the staff decided to stop her 1mg Lorazepam that she has taken every night for many years because the new GP mistakenly wrote 'Take one at night when needed' and staff are now following PRN policy.
After I expressed my concern an emergency appointment was made to see a (new) psychiatrist who stated that because she had been on the Lorazepam for so long it would probably have no effect on her and to continue it as PRN.
We would rather she was tapered off it than given randomly. They administer 1mg if unsettled 20 minutes before bed - or administer 1mg if awake and anxious over a 20 minute period during the night.
Although family disagreed we gave the staff the benefit of the doubt but was shocked when we visited my cousin after 5 weeks to see she is ripping her hair out, is screaming and screching for much longer periods and has lost almost a stone in weight.
We know her well and the sad thing is she has no voice and relies on the kindness and understanding of the staff who unfortunately did not give themselves time to get to know her or allow her to settle in before they withdrew the drug and the decision to give or not to give is left to support workers.
I know 1mg is a low dose but I do believe she is having withdrawal symptoms because it was suddenly stopped and then only given now and again, sometimes at 4am and then not for a few days or even a week and then given again.
We feel that nobody understands our concern and they think we are being over protective.
I'd be interested in anybody's thoughts on this. We just want her to be happy and well looked after but I am wondering if it is too much to expect.