Hospital Disaster

Over the past couple of months i have been having numerous hospital appointments and then had an operation. It was to remove 4 teeth (3 wisdom teeth and one other tooth).

It seemed to be one disaster after another. Although the operation was successful it was not without drama, trauma or stress. They really did not seem to have a handle on how to deal with Autism at all and has left me having nightmares about it.

It all really started with a mix up with hospitals. I went to Fairfield Hospital to see the surgeon and have xrays done. I then had a further appointment for MRSA screening as part of the pre-op before the operation, I turned up at Fairfield hospital to be told the actual appointment was at North Manchester hospital. So this test was rearranged and i went to North Manchester Hospital, to have the test done and was given an operation date and letter saying the Operation would be done at Fairfield Hospital. It really didn’t help that all the letters came from Fairfield hospital, including the one for the appointment at North Manchester Hospital. All these appointments happened within weeks. Not very helpful and quite an information overload.

I received 2 letters in the post regarding the day of my Operation. The First one said I had to be at the hospital at 12 noon for an afternoon operation and the second letter arrived on saturday afternoon before my operation on the Tuesday (monday was a bank holiday) to say I had to be there at 7:30am for a morning operation. Due to the Time of arrival and the bank holiday i couldnt contact the booking department to find which time i was meant to be there for, so we took the 2nd letter as the most up to date and went to the hospital for a morning surgery.

I wasn’t allowed anything to eat or drink from 11pm the night before. We arrived at The hospital and checked in at 6:45am. The little waiting room was very hot and stuffy. The receptionist behind the desk was eating her Breakfast and drinking cups of tea in front of patients who were nil by mouth which I thought was quite mean. I was already quite nervous and anxious before arriving at hospital and at around 11am nothing had happened and was still sat in the waiting room. I went up to the receptionist to find out if they had forgotten about me and after she looked into it i was told i was not due to have my operation until later in the afternoon and apologised that no one had told me. During the time we had been there we had seen other people being called in and some already coming back from their operations. At around 11:45am i was on the verge of having a major panic attack as i had been trying to hold it all together since the night before. After discussing it with my partner i decided that i was no longer in a fit state and really didn’t want to have the operation that day, I had reached my limit. I wanted to cancel it and rearrange for another less stressful day. So i went to speak with the nurses and asked to cancel and rearrange, i was asked why and i had explained i had autism i’ve been waiting for almost 5 hours with nothing happening, hadn’t eaten or drunk anything in 12 hours and was starting to have a major panic attack. The nurses really didn’t want me to cancel and tried everything to get me to stay and said they would ask the surgeon if i could go next instead of having to wait until later. I really did feel rail-roaded into having the surgery done.

The surgeon agreed to change his schedule and I was then next in line for surgery. I met with nurse’s, the anaesthetist and the surgeon. I was asked multiple times about my current conditions and medications, which I explained about my autism, PTSD, anxiety and depression. I was then taken down to the operating theatre around 12:40pm.

While I was in theatre my partner was sat waiting in the waiting room, he received a phone call from North Manchester Hospital asking him where he is and could he come into hospital as there was a problem with my surgery. He explained he was sat in the waiting room of the day surgery unit, so they said they’d be down to collect him. Around 10 minutes later he gets a call back as they can’t find him and he explained he was by the reception desk of the day unit at Fairfield hospital. For some reason they were looking for him at North Manchester Hospital. The switchboard was at north Manchester so they had assumed the surgery was being done there.

Once the confusion had been cleared up, A staff nurse came and collected him and took him into the operating theatre where I was and he was horrified to see me being forcibly held down and me “fighting” to escape. There was nurses holding my arms and legs down and others trying to keep the oxygen mask over my face. He explained that i had autism and they needed to stop as they were doing to much at once. He also explained about my medication and my anxiety, depression and what i had been through that morning. They hadn’t been told any of this, despite me confirming it numerous times that day. I remember bits of this as I started to come round during the operation. Apparently I had a bad reaction to the anesthetic due to the medication I was on. So they had to bring me round during the operation in order to give me a different type of anesthetic. My partner was told verbally what anesthetic I had a bad reaction to and was told that in future operations I should not be given it, however this was written down.

The operation which should have only been half an hour turned into a 3 hour one, once done I was taken back to the day unit. Instead of being put onto the ward to recover with the other patients. I was put into my own room in order to come round in my own time. Everything seemed to change at that point, myself and partner were treated with ‘kid gloves’ lots of tea and extra biscuits. Everything done at my pace. They seemed to be falling over themselves to be helpful, it seemed like everyone knew something had gone wrong and were trying to make up for it.

After hours recovering I was discharged and sent home. It was days later, when the swelling had gone down that I could see there was a stitch in one of the wounds and a week later another stitch came out.

No one had told me I had stitches put in (how many, how long they’d last etc), I wasn’t told by any hospital staff what had happened in theatre or what anesthetic I need to avoid (hopefully this will be on medical notes). As I will need to make people aware of this in future. Now feeling left very let down, traumatized and have loss quite a bit of trust in hospital.

Throughout my treatment from my dentist, to the consultant, the pre op appointments and the morning of the surgery. I told everyone I was autistic and had other health issues, but it all seemed to be ignored on the day.

There are however 2 silver linings throughout this ordeal that I can take comfort in. Firstly, the painful and troublesome teeth have been removed and secondly, how my confidence has grown (through the help of life coaching) in order to stand up and say I wanted to cancel and rebook, despite being forced into it, previously I would never have stood up for myself in that way.

So all in all a disastrous hospital trip with NHS staff needing a lot more autism recognition and training. Being overwhelmed with information and dates at different hospitals and lasting nightmares about being held down and ignored however I will seek treatment for it and will give feed back to the hospital as no-one should have to endure what I was subjected to. It would be difficult for a normal person to deal with let alone someone on the autism spectrum.

Where to start?

Argh! Don’t know where to start or what to do for the best. I have so many different issues both physically and mentally that need addressing. I have noticed however all these issues overlap and interact with one another. The way the mental health team and the GP work is to focus on one issue at a time. Which in theory would be a good idea, but by doing this its causing different issues to get worse or has unintended consequences.

I have just finished an ‘Anxiety group Workshop’ course of treatment. To be honest I think it made things worse than it did in actually helping. It was good to find out and hear from others that they were experiencing the same anxiety symptoms as I was (although for different reasons) so I learnt that I wasn’t alone and that I shouldn’t be so scared of the symptoms of anxiety. But it did show how bad and deep my depression was, we had an exercise where we had to challenge ‘negative thoughts’ and turn them into positive ones. For example I’m nervous of going out of my flat. “Something bad will happen if I do” so we had to change it into a positive thought “something good will happen if I go out” but I found that although I could make up something and change it into a positive I didn’t actually believe it and just made me more depressed.

Things that need to be sorted:

Depression – Have had depression for around 15 years, It comes and goes but is always there. I was in an abusive relation for 6 years, in a job that i was constantly bullied in for 10 years. A lot of people have taken advantage of me and my good nature, which makes trusting new people difficult. Have struggled with coming to terms with my sexuality, and struggled with my disabilities – Dyslexia, Hearing loss, musculoskeletal issues, mental health issues. and often depressed about money. Feeling low increases my anxieties. I have been suicidal and don’t want to fall back into that.

PTSD – Still getting flashbacks and nightmares of the events in 2013. This increases my anxiety and depression.

Anxiety – Because i’m anxious all the time and have physical symptoms (sweating) and panic attacks means I often don’t go out, makes me feel guilty and stops me from doing the things i used to enjoy and this makes me depressed.

Health – Due to musculoskeletal issues I’m constantly in pain, which makes my mood low, I tend not to go and get anxious that if i do go out i’ll be in pain or make it worse and i’m not in the right mental state to face surgery on it. I’m on 13 tablets a day, which i know is a lot and proves to me everyday that i’m unwell and increases my depression and my anxieties. I’m very conscious of my hearing aids and how people might react to it.

It’s only a brief description of the things i need sorting, because theirs lots more involved and i’m not comfortable sharing or bringing up everything at the moment, hopefully will give people an insight into how everything is interlocked and overlapping. So when your focusing on one single issue the other issues get worse, and its like taking one step forward and 2 steps back. GP wants to know how i want to move forward with my treatment and what i want to focus on, but i really don’t know as everything is connected. Nothing is worse than anything else, they are all as bad as each other. Ideally would need to work on all of them at the same time to slowly reduce the effects but the Health system doesn’t appear to be set up to accommodate that.

Starting to move forward again

Well things are starting to move forward again, after grinding to a halt.

I Have received my appointment for the Orthotics Department, Was referred to them back in January 2016 and was told of a 9-13 month waiting list, but its come through after 6 months months so hopefully will be able to help. Although i am meant to be doing physiotherapy along side this, but that still up in the air between the mental health team and the physio departments.

After speaking with my GP and saying i didn’t think that CBT (Cognitive Behavioural Therapy) was right for me at this time. I was referred to the Healthy Minds team in Bury. And Have an assessment next week with a Psychological Wellbeing Practitioner. Hopefully will be able to get someone for me to talk through things, as thats what i think i need and have been trying to get since 2013 without success.

Also Purchased a new pill box for myself:

pillbox

As I Take 6 pills of different medication daily (42 a week, 168 a Month!) I kept getting confused with which ones I had or hadn’t taken that day. Put now can just have a quick look and i’ll know. Also saves lots of space as don’t have big boxes stacked on each other anymore.

All Small Things, but all positive.

Asking for help

After speaking with family down in London, Went to GP and told her that I didn’t think CBT (Cognitive Behaviour Therapy) Was right for me at this time, I needed someone I could talk through my thoughts and feelings with. So I Have been referred to ‘Healthy Minds Bury’, so will see what comes of that. Also mentioned that i’m having mood swings and that my mood is normally a bit flat / nonchalant mood. So have had my medication increased. (6 pills daily now).

Been going regularly to Bolton Hospital since January for the dizzy spells I’ve been having, from when I fell and hit my head. Although they found that i had damaged and lost my some of my hearing, Reason why i know wear a hearing aid, but it seems that the dizzy spells i have been having are a symptom of anxiety, but GP didn’t want to do anything else as that’ll be for the Healthy Minds team and medication to help control.

So fingers crossed, hopefully be able to move forward again.

Health Update

Health Update:

CBT: (Cognitive Behaviour Therapy)
Had my first (and last) session yesterday. They are unable to help at the moment due to physical issues and high pain levels. As part of the CBT process involves mobility and as I’m in pain it will apparently distract me. So have to get my knees sorted before they will work on my mental state. However surgeons won’t help till my mental state is better. Catch 22. Waited 12 months for this to be told no, had it happened earlier i might have gotten it done.

Physiotherapy:
Went to physio today. Very painful. Apparently I have issues with my hips to add to my knees and feet. They are weak and rotating my legs more than they should. Been given exercises to complete over the festive period and have to go back first week of January.

GP:
Doctors keeping my current meds the same but given me more pain killers. Takes my total of pills to 14 a day.lol

Physical Illness Vs Mental Illness

Mental Illness rules my life, whether i want it to or not. However I have been suffering alot of physical issues too. I never know it its part of my mental illness, or side effects of medication. Everytime i’ve gone to see the GP, my mental health has been my priority cause of the state i’m in. I have let things slide, they were only small issues that i could ignore as they weren’t a major issue. But now i got to the stage that they have all built up and now causing bigger issues.

I have also been afraid to speak to the GP about it as, i keep feeling it’ll just be boxed off as ‘Mental’ issues, but after speaking with my Doctor it turns out there was some serious issues:
– Got a fungal infection on my foot so been given some Daktacort Ointment to help clear it
– Had ringing in my ears since my collapse in 2013 when i knocked myself out. GP’s gonna refer me to the hospital to see an ENT specialist.
– Got 3 moles , 2 on my forehead and one on my side that have started to grow lumps. Doctors not worried so been booked in for minor surgery to have these removed. No date as yet
– Also having lot of pain in my knees and my reconstructed one ‘crunches’ when i bend it. So going back next week to GP for a full exam and so she can go through the x-rays from the hospital.

So hopefully well get some things sorted.

Advice, Assistance, Directions…

instructions-directions-advice-assistance-four-way-intersectio-words-road-signs-intersection-to-help-you-find-42614989

I don’t know what to do for the best…

When i finished my last counselling session in 2014, i was starting to get back on track and finding my way again. The sessions helped with my PTSD. My flashbacks and nightmares were the biggest challenge at the time. Then in January 2015 i felt strong enough to get help for my next issues which was anxiety and my GP Referred me for CBT (Cognitive Behaviour Therapy). Which I agreed was right for me at the time. However i was expecting a 12 month waiting list. I’m now 9 months in and social anxiety is my biggest issue, however I’m not sure that CBT is now right for me in my current state of mind. I think talking to someone about my anxieties and things that had happened in my past (domestic abuse and past issues) that seem to be running rampant around me mind at the moment.

I’m scared of saying anything to my GP or asking for different help, cause i really don’t know what is for the best. I don’t want to end up in the same situation, if i cancel or change the CBT, i might then go back on a waiting list for another 12 months and that wont help. But at the same time, doing counselling/CBT when your not ready for it or in the right frame of mind, is also dangerous. (Numerous GP’s and mental health people have said this).

I feel i’m not only letting myself down, but letting friends and family down. Everyone wants me to get better ASAP, even though there is no official timescales for recovery. I don’t want to be a burden, a worry or a cause of stress for anyone.

There is always the crisis team, which i know have helped others before, but without a GP or someone referring me, i feel like a fraud asking for help. I just don’t know what to do or where to go!

 

Lost

Been feeling very lost lately. Still having trouble planning for the future and my social anxiety seems to be getting worse. I don’t feel safe or comfortable going out the flat. Not sure where its come from. A Lot of it predictably is in my head, feel i’m being judged by everyone and i feel some how that i’ve got a big label hanging over me saying “Hes nuts, stay away.”

Have a lot of support on facebook, twitter and other sites i’m on across the internet. A Lot of people wanting to meet me and say hello. I’ve never been great at ‘first contacts’ and with my anxiety since my breakdown its a huge barrier. I would love to meet some people and get out more, its just trying to cross that barrier that’s difficult. I’m still on a waiting list for CBT (Cognitive Behavioural Therapy), which has been months, hopefully will be able to chase it with the GP this week.

My Left knee has been acting up again. I had it reconstructed in 2010 and its been pretty good, but think it dislocated and popped back in, bruising and swelling suggests this too, GP’s given me lots of pain meds, but yet another barrier to getting out as i cant bear weight on it.

On the positive side of things during the late May bank holiday, i went with my BF and parents to Liverpool to see Cunards 150 Year anniversary 3 Queens event. Over 1 million people descended on Liverpool. There were crowds everywhere and tbh i didn’t cope great. Think i was able to mask a lot of it. but got to the stage where everyone was concerned and knew it was causing me issues (except for the crowd stewards who refused to help u, when we needed it).

 

Almost Christmas…

Well Quite a week I had last week, Went to see the GP on Monday as had been feeling rather low, kept having dizzy spells and had a sore throat. Doctor increased my medication and gave me an oral solutions for my throat. Turns out i had been brining stomach acid up during my anxiety/burping fits and had damaged my throat.

Tuesday i was not feeling great at all. Very dizzy and and very low on energy, managed to make it through most the day but then collapsed in the kitchen. Luckily was able to shout my partner before i fell who managed to catch me. He called 111 for advice and they sent out an ambulance. Very lovely and understanding ambulance crew. had loads of tests done and an ECG. But they think it was a combination of exhaustion, increase in medication and anxiety attack. Took me a while to get back up to full strength but getting there. Hopefully that’ll be enough of the excitement this year (fingers crossed).

Almost ready for Christmas, cant believe its only days away. Cant wait, am so excited. Unfortunately wont be going home to see family for Christmas but will see them for New Years.

Wishing everyone a very Merry Christmas!

Christmas

Guilt…

I feel so Guilty that i’ve had a breakdown and its affected my friends and family. In ways I couldn’t have foreseen or planned for.

I know I shouldn’t. I know i’m unwell and will get better but it doesn’t stop the guilt.

Friends and family have been brilliant and supportive, So huge thank you to them.

Others have distanced themselves or disappeared completely.  Some I think just don’t know how to react or feel i’m pulling them down. My Moods can change at the drop of the hat, but is a lot better now my new meds have  started working. Hopefully will start connecting and building friendships back up.

 Slow small steps but any progress is good.

This song from Matchbox twenty suits me, “I’m not crazy, I’m just a little unwell”

Unwell

Getting Help with Mental Health….or not…

It is scary, when you need help and there’s no-one there.

There are charities and organizations out there:

Anxiety UK

Mind Charity

Time to Change

 

Unfortunately I have found that a lot of the help out there you have to go and find yourself. When your nervous of social situations and terrified of using the telephone it doesn’t help. Quite often it feels like you just have to be quiet and get on with it but not disturb anyone else with it. Which in the 21st Century is really disgusting!

We had the Greater Manchester Police (GMP) come to our flat as they were ‘Concerned for our welfare’ back in February 2014. We were put on a ‘Vulnerable Adults list’ Were told we’d get a social worker and guess what, nothing happened.

My Doctors Surgery depending on which doctor you see sometimes helps. But when going in and being asked “How can i help you?” when you’ve explained everything going on, doesn’t really help, if i could cope and knew how to fix it i would have already. Trying to get medication from them is difficult as well, because the medication is strong, it cant be put on repeat prescription, i have get an appointment and go into the surgery every time to see the doctor. Which i can understand. But there are no appointments available currently and they would re-order medication over the phone (understandably), but leaves me without medication. So all the work and progress i’ve made could be unravelled.

My Local Council ‘Bury County Council’ Doesn’t seem to have anything set up for people with Mental health Issues, not that i have found. I have asked them on numerous occasions through a variety of different means and they have responded with silence. As with a lot of services is they do have anything its either not on there website or hidden away under loads of different options. The Mind Charity has recently written a report which reveals an ‘Unacceptably low spending on public Mental Health.’ (See the report Here).

Although i agree at times i’m not able to accomplish anything but with the proper help and support not just me but other sufferers would be able to recover or at least cope better with the Issues and get back into society which surely would be good for everywhere. Why people see Mental health as a taboo and something to be brushed away out of sight is beyond me. Hopefully attitudes will change.

Sleeping Issues

Been having a huge amount of Sleeping problems since the events in November 2013. I used to struggle to function if i didn’t get a good 7 or 8 hours of sleep a night, would wake up grumpy and tired if i didn’t. But for the past 10 Months I’d be lucky to get 6 hours a night. And even then its not full restful sleep. Its unbroken and difficult. Although on the plus side do get to see some lovely Sunrises over Manchester as I’m still awake as the sun comes up (chance for a Twitter or Facebook upload).

Suffering from lack of sleep is horrible. It brings your mood down, you cant concentrate on anything. Everything is so much effort and there is just no motivation at all to do anything.

I’ve been having Counseling through Bury IAPT services for the past 3 or 4 months to help with my flashbacks and nightmares that started after my breakdown.  This has helped to control my nightmares and Flashbacks but they still appear from time to time, Classic symptoms of PTSD. The main flashback that troubles me is one of the memories i had when Greater Manchester Police (GMP), first came to the flat and made me think that my Fiancee and love of my love had died. Its of a police officer that was stood in my the flat. in a certain stance, he was wearing full police uniform including high-vis jacket. And had his arms up holding onto the top of his stab vest. This image haunts me. The Police tell me Officers stand like that cause its more comfortable as the stab vest and equipment they have is uncomfortable. But i saw it as a very aggressive stance. It looks like his fists were up and ready for a fight and he was ready to launch at me any moment.

The Nightmares are truly awful, waking up covered in sweat, heart pounding, jumping up and screaming. The nightmares although were different in scene setting, people in them but there are 3 main themes which keeping troubling me and keep coming up time and time again. The first one is seeing Police in my nightmares, this would start of my anxiety/panic attacks and after waking i wouldn’t have a chance of getting back to sleep. On numerous occasions the Nightmare of the Police raiding the flat or me opening the door to see a policeman there, would require me to get dressed and walk around the block to confirm that there are no Police nearby, this sometimes stops the panic attacks but rarely stops the anxiety attacks. The policeman is always the same, same face, doesn’t matter what I’m dreaming about he’ll walk my nightmares to find me. The second theme again stems from the PTSD and the thought that my other half had died. In the nightmares I’m loosing someone close to me. friends, family the person who dies or goes missing is always different but the emotions and feeling of loss just brings me back to the way GMP left me in November after the first visit they paid me. The emotion and feeling of loss is huge and very dark, Some very dark places and thoughts come after these nightmares. The 3rd theme is quite simply fear. Just being afraid scared of everything and anyone, again down to GMP and me loosing my ‘safety net’, no-one is there to help or protect me and this leaves me feeling very alone, very vulnerable and very scared.

At the moment i have no sleep routine, I sleep when i can and when needed. I still try and go to bed and sleep but normally just lie there for hours in between 20 minute power naps. I’m constantly tired and not through lack of trying to sleep. Back in December the GP put me on medication (Zopiclone), some strong sleeping tablets. I was only allowed that one prescription of it (28 tablets) due to them being addictive. They did allow me to sleep for a good uninterrupted, restful time.

Although the flashbacks and nightmares have improved with the help of counseling. Its not just the sleeping that’s an issue. My Anxiety disorder is next on the list that i need to get help for. I’m actually scared/worried of waking up. As silly as it sounds, but when I’m asleep, no one can hurt me. There is less people about at night and generally less noise so allows me to get things done and completed without jumping at every noise from outside or elsewhere in the building. In November the 2 days the Police arrived at the flat they woke me up and got me out of bed. So I’m extremely anxious in the mornings. This could be why i stay up all night before going to sleep when the sun comes out. Then again when my Partner Mike was having his flashbacks/rough/dark times they generally were at night. So I’m not sleeping as heavily as i was to listen out to keep me eye on him.

So really my Sleeping issues are a mess. And that’s just the mental health side of things troubling me when i try to sleep. Not to mention the back or knee pains.  [whohit]Sleeping-issues[/whohit]

Waking up with an Anxiety disorder

I wake up most morning normally with a jump/start and so the day beings. Every morning starts with physical symptoms,  a racing heart and shakiness. The shakiness has calmed down a lot since November, but still affects my life in a massive way. The GP Has put me on Beta Blockers to slow my heart down so I’m not in such a panic state all the time, and although it does have a large affect it it is still very noticeable.

I’m so scared of what the future may hold. my life was turned upside down by Greater Manchester Police, through no fault of my own. If i had done something i could understand it, but i didn’t and nothing can stop it happening again. So scared of going out, every where i go now i always purchase something along the way so i have receipts i.e. a paper trail, to follow so people cant say i was some where else. This is not a nice way to live.

After getting up and checking each room in the flat (just to make sure no one is there) i have my morning brew and my cocktail of medicines, all prescribed by the GP. It’ll normally take me a couple of hours for me to calm down and stop panicking after waking up before I’m able to do anything productive. On really bad days I’m just pacing the flat back and fourth, if the fight or flight response is too difficult to ignore. Then i will go for a morning walk around the block, Mainly to check that there are no Police around (a fall out from November again).

Once I’m calmer and more in a stable state of mind then i can get up and do things, not massive things everyday things like washing and cleaning.  At the moment I’m only really going out the flat either for a walk to calm me down (which doesn’t stray to far from the flat), or I’m going to GP, Hospital, or Counseling appointments. All the fun stuff i used to do like go shopping, Going out with Mike on the Bike, or going to Transport Festivals. I no longer do in case i meet a police officer, i don’t know how I’d react. I’d have a panic attack and either run away, causing the officer to chase, or the officer would have to deal with my panic attacks calling paramedics and probably causing more stress. Hopefully next couple of weeks I’ll try and get to the Bury Transport Museum or Manchester’s Transport Museum. Used to love both of them. But depends on my state of mind and current financials (living on benefits is not as easy as people make out, but that’s for another blog maybe).

Most days is me trying to find things to take my mind of things, e.g. Baking cakes, Puzzles or computer games and of course my Blog (hello there my dear readers 🙂 ). Other days after waking up i don’t feel i can keep myself safe, in a sense that I’ll lash out at something or go do something silly, So I’ll just stay in bed and try and sleep cause tomorrow has to be better. Mike by other half is brilliant on these days always keeping me engaged and keeping an eye on me.  [whohit]Waking-up-with-anxiety-disorder[/whohit]