Almost all of the work on this blog and on twitter is being done by a small group of people, with a much wider group of people supporting us.
We've had 3 - soon to be 4 contributions from local service users about their treatment and what being treated locally means to them and two anonymous contributions from people working in the trust.
Here are the top 5 reasons for not contributing, in ascending order.
5. Someone in my family works for the Trust and I'm scared they will lose their job.
4. Nothing will happen so what's the point? The Trust doesn't care about us, just money.
3. I'm just too ill to deal with this right now. I want to help, but I just can't.
2.I'm scared that if I share my story, someone will read it and know it's me. I don't want people to know I've been to Ridge Lea.
1. I'm scared that even if we DO get the beds back, if they know I'm involved, next time I'm ill, they'll send me away to punish me for speaking out.
So that's fear if being punished, fear of being judged for having a mental illness, fear for your family, despondency and illness.
Thank goodness some of us are able to stand up for those who want to, but can't.
Showing posts with label fear. Show all posts
Showing posts with label fear. Show all posts
Saturday, 8 November 2014
Sunday, 2 November 2014
Clare's Story - A near miss, distressed children and a fear for the future.
In April 2014, I was assessed in A&E under the Mental
Health Act. I’d been depressed for a
long time, but the descent was long and slow, until it reached the point where making plans seemed like a perfectly rational thing to
do. Fortunately I had a good friend who
knew it was absolutely not a rational thing to do, so she took me A&E with
me protesting all the time that no one would believe it and it was a waste of
time.
After being assessed by the MH liaison nurse, I was asked if
I would go into hospital, but the only bed available was at The Priory in
Manchester, a private hospital well over an hour’s drive from where I
lived. I refused as I didn’t want to be
so far away from home with no possessions and no means of my husband getting
there, as he had our two small children to look after. In the end they decided not to detain me, but
pass me over to the care of the local Crisis Team.
Like Crisis Teams all over the country, they are massively
overstretched and a decision was taken to leave me in the care of the community
team as I was seeing my psychiatrist the following afternoon. By mid-morning the following day, I was
waiting on the platform of the station for the London express train, however,
the same good friend as the day before had sent her husband speculatively to
see if I was there. That was the near miss.
If a local bed had been available the day before then I would’ve been in
hospital, safe.
Thankfully this time there was a bed in Ridge Lea hospital in Lancaster and I was admitted and stayed there as an inpatient before the
hospital was closed and all of the patients transferred to The Orchard, the new
unit in Lancaster. I was in hospital for
around 3 months.
The impact of my admission on my family was enormous. My son has autism and was extremely disrupted
by my being away as it changed his routines. His autism meant that couldn't express how he felt easily, so he got cross every day. His home to school diary was filled with
examples of him being upset by my absence and struggling in school. My young daughter didn’t remember the last
time I’d been admitted as she’d been too young, but this time she was very
aware and her behaviour became very difficult as she struggled to come to terms
with my being in hospital. She became
clingy to everyone else in the family and anxious that I would never come back.
The only thing that made it better for them was that I was
still close by. My husband bought them
up nearly every day after school and nursery and we got to spend time together,
even though at the time it took monumental effort for me to be ‘normal’ with
them. As I got better and had leave, I
was able to go home to dinner, or do bedtime with them or all the small things
that a parent does for a child.
Sometimes this was more for their benefit than for mine as mental
illness takes away some of the person you are, but to them it meant everything.
If I had been at a hospital miles away, none of that would
have been possible. My children’s
struggles would have been even harder.
The visits would be more sporadic with long journeys to get to see me
and the impact of my absence would have been amplified many times over. At the beginning, my only motivation to get
through the day was the obligation I felt to see them. As I got better, that changed to wanting to
see them as I missed them, till eventually I was discharged.
Even when they are unwell; mothers need to be near their
children and children need to have regular contact with their mothers. Isolating me from my children would have
caused distress on both sides, but now this is what would happen if I was
admitted again.
Getting ill again already scares me as it has had a huge and
lasting impact on my life emotionally and financially and has shaken my whole
world. Now I have the additional fear
that if I get ill, I will be taken away from my family, my friends and everyone
who means anything to me. I will be ill,
alone and isolated from the very people I need to support me to get well.
Closing The Orchard to women like me, may mean more near
misses like mine as they are too scared to take help knowing they will be sent
away. Speaking to other women in the community, I know I am not alone. Fear when you already have a mental illness is not good. Not good at all.
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