Showing posts with label accessible. Show all posts
Showing posts with label accessible. Show all posts

Tuesday, 1 July 2014

Disability Facilities Grant – discriminated against yet again.

Introduction.

Many readers will have followed our struggles to find a wheelchair accessible home in Spalding Lincolnshire. So just to recap, we have tried to help ourselves by:-
  1.  Private rental but nothing out there ready to move into, and landlords will not give you a long enough tenancy to apply for the grants for alterations needed.
  2. We are currently on SHDC s waiting list, but again they do not have suitable properties on their books, and they are about to change the rules so that our local connections will not be local enough anymore. We currently have the maximum points for a medical grounds move.
  3.  We are on numerous housing charities waiting lists, but they do not have properties in Spalding where we want to live.
  4. We spoke with the organisations that report to help the disabled with specialist mortgages, but because I am of working age, likely to return to work, not disabled myself, they will not help us.
  5.  Have tried to educate and make local politicians aware that the system is not working for the poorest, most disabled in society.
  6. We found an organisation, MIVA Partnership that are trying to help us, but once they get this latest news I think they will run for the hills. They proposed buying a place for us to adapt and rent off them long term. Their biggest struggle is getting the necessary finance so that they can make the standard buy to let return ratio of 8%.

Update.
Two weeks ago we thought we had found an ideal property to alter for Hubby’s needs. Just so you know we are not looking at palaces it was at the £120k mark. Our contact told us to start the ball rolling for the Disability Facility Grant as the property would need some substantial alterations to make it suitable for partially tetraplegic (paralysis in all four limbs) Hubby, me and our care team. Our contact in the housing team at SHDC sent a referral for us to the Lincolnshire County Council OT’s based in Lincoln.
Today I had a very depressing conversation with one of the OT’s where it has become very apparent that we do not stand a snow ball in hells chance of getting any financial help, not because we do not qualify but because the procedures in place are so rigid that they discriminate against the most disabled and poorest in society.

Why do I say that ?

1.       I was told , the whole grant procedure can take 5-8 months to release the monies, meanwhile you would have to live in the property.

                        WE can not do that, I would be putting my Hubby in physical danger if I did that. He can not go 5-8 months without having a shower, not being able to gain access via ramps to the property, not being able to access several rooms due to door sizes, etc. Also he is not well enough to live on a building site. I also have to consider the Health and Safety of our care team and myself come to that. Working in confined badly designed spaces is an accident waiting to happen. I am in constant pain at the moment because my back is close to giving out on me, due to all the manual lifting I have to do, in our currently badly designed space.

2.       What private landlord is going wait 5-8 months before he gets his monthly rent ?

NONE ARE.

So it looks like to me , that unless you own your own home, and are therefore not the poorest in society, there is no help for you to ensure that you live in a safe, and accessible home.

In Summary.

CAN SOMEONE PLEASE EXPLAIN TO ME WHAT SEVERELY DISABLED PEOPLE WHO NEED TO RENT ARE SUPPOSED TO DO, as I have run out of ideas?

Most people when we tell them what has happened to us, can not believe that in BRITAIN today we do not look after our most vulnerable, what does that say about the society we live in.


Please RT this, copy it, spread the word, people need to know the present system is not helping the most needy in society.

Wednesday, 29 January 2014

Housing and Care a User’s Perspective.

Introduction

I am writing this to give those working in Housing and Care one users perspective of what is wrong with the current system and why it does not work for us and from what is seen, heard, around us does not work well for others as well.

Background

Back in 2009 my then 64 year old husband qualified for NHS Continuing Care, having been infected in his neck with Staphylococcus Aureus which caused crushing of his spinal cord, leaving him a partial tetraplegic with the added complication of having only one kidney as the right one was removed due to cancer. He has lots of medical complications caused by his spinal cord injury, is very severely physically disabled, cannot walk or stand and has limited arm/ hand function, needs help with all bodily functions, but is very much fully compos mentis.

We had recently returned from working abroad so to get local social services help had rented a totally unsuitable bungalow where Hubby had to be bathed in a paddling pool sat in his commode, stretching the shower hose over him. So when we were moved to the fairly new first floor flat in a development at an extra care facility, we were relieved to have at least a very small wet room.

Very soon after moving in we realised what a huge mistake we had made.

·         The master bedroom is not big enough to take a hospital plus a single bed for me at weekends when I am in charge of Hubby’s night care. Not big enough to allow care workers enough room to safely use a mobile hoist and be able to access the bed all around for using sliding sheets etc.  This has meant that I feel I have been forced to use a very dangerous to me manual lifting regime to get Hubby in and out of his wheelchair / bed. The room is carpeted which is causing difficulties in keeping it hygienically clean, water transfer from wet-room, accidents,  wheelchair tire tracks. The building construction means there is nothing solid to attach either a ceiling or wall track hoist.

·         There is a lack of storage space which means when I sleep in the spare room I have a usable bed which is surrounded and crowded out by stuff that we have nowhere to put. No secure storage for bicycles (my hobby), lack of built in wardrobes and not enough space to be safe in the flat and build some ourselves.
·         The wet room is so small that we have had some accidents when manoeuvring him in his shower chair, painfully catching my fingers, Hubby’s knuckles and toes.  

·         All of the doorways are so narrow that Hubby has to be extremely careful when lining up his chair to get in and out of the two rooms that he uses.

·         Our living room is too small to take a sofa, chairs and Hubby’s wheelchair plus the two side tables he needs so that things are within his reach.

·         All of access in, out and around our flat is very difficult to manage so Hubby is in effect imprisoned in two North facing dark rooms except for the occasional trip out for hospital visits.

·         Only access is via a lift that is so small that in an emergency it will not take an ambulance trolley. Also when we venture out I have to send the lift down and run down the stairs to meet it.
·         Our care workers when here sit at our small dining room table, with no proper storage place for their files and paperwork.

·         One luxury we have is a second bathroom which gives our care workers a separate hygiene area, and somewhere to store the hoist that they have to use. Not really a luxury as our home is their place of work, we don’t want to share a toilet with them. Accidents happen as well and they need some where to shower and change. It also means that I get to soak my over worked family carer aching bones in a hot bath now and then.

·         Our kitchen is totally inaccessible to Hubby.

·         A couple of years ago our housing association thought it a good idea to take away the wooden threshold strips leaving a 1 ½ inch gap under the door which then sucks into our flat the second hand cigarette smoke of our neighbour. Not an ideal living arrangement for a tetraplegic who is on the very limits of being able to breathe unaided. Also she is an added fire risk that with limited evacuations options is not acceptable to us.
Since writing this in January, our next door neighbour set her flat on fire, sadly losing her life. Despite what was reported in the local paper we did not have a safe exit option, we were trapped in our flat while they put the fire out. There was dense smoke blocking our only exit from the flat. It is even more urgent that we are moved to some where that is safe.


Needless to say we are both totally fed up with living somewhere that is totally unsuitable, is not enhancing what little life Hubby has left, and putting me as his carer at physical risk.

The Challenges

So what have we done to try and remedy the situation?  Three years ago we met with a council OT, who agreed that in principle we were housed in the wrong environment, were awarded the maximum points for a medically based move. Looking back on the interview, with the hindsight of doing more research, I now realise, from the way we were spoken to, that we were being condescended, that our concerns were not being listened to, but being replaced with pre-conceived notions of where disabled older people should live.
Since being on the housing list we have met with the obvious attitude that “you should be grateful for a roof over your head”. People in general do not recognise that disabled people should have the same choices as everyone else as to where and what kind of place they want to live in. This is obvious with the few places that we have been given the option of looking at. OAP bungalows with even less space, houses with tiny internal wheelchair lifts that Hubby cannot operate safely etc. It is becoming very obvious to me that no one has thought to build or adapt existing bungalows to meet the growing need for disabled wheelchair users that maintain their independence in the community by making use of care teams. Local Authority teams do not recognise the different space requirements of totally independent wheelchair users and those that need a care team.

The other day I looked at the floor plans for a new over 55 development in Bourne Lincolnshire. Not one of the floor plans had a bedroom big enough to accommodate 2 single beds plus wheelchair manoeuvre room or a separate hygiene area for care workers. Everyone seems to think the elderly and disabled want to live on a postage stamp.

So having increasingly despaired with the social housing market I turn my sights to private rentals. We would have to contribute more to our rent as the housing benefit allowances for private are not as generous, but as I fully intend to return to work as soon as possible this is not a big issue if we can get a landlord to work with us to make a bungalow accessible. We came across somewhere that we could have made perfect for our circumstances, it needs some alterations for has lots of potential. We got past the first hurdle of the rental agencies that usually suddenly make the property unavailable to disabled enquirers, got to speak to the landlord to explain our situation. He seemed very understanding of our plight, I explained that we would need to change the on suite bathroom into a wet-room out of our meagre savings, then once moved in apply for a disability grant for the other changes that we needed.  Also that longer term if my work situation panned out we would look to buy it off him. I also explained that we would need some sort of secured tenancy as to apply for the grant the council want to know you can live in the property for five years. Anyway we left the conversation at that point, as we had to involve the estate agent he was using to manage the rental. So I talked it through with the agent explaining the different type of rental agreement we would need, as she had no experience of other types other than the short-hold, 6 month, 12 month assured tenancies more usual in the private rental market. The estate agent and landlord subsequently had a conversation and unfortunately the landlord was not in a position to grant us a 5 years short hold or an assured tenancy so our perfect property fell through.

This means that in most cases the private rental sector is totally unavailable to mobility restricted renters, but the local authorities / social housing associations are not providing it either, does not sound very equitable or fair to me, or looking after our most vulnerable in society, does it you?

Still we have not given up, we found a company that sounded promising at first. They said they would find an investor to buy somewhere for us, for us to rent from them. This company so far has failed to find such an investor to help us.

Then I heard about a scheme for part ownership / part rent shared ownership scheme especially for disabled people on benefits. Guess what no help there because Hubby is over 65 and because I hope to return to work.

A Way Forward.

With the pooling together of Health and Social Care I am hoping that local authorities will feel more obligated to get housing right for those that have care teams. There needs to be recognition amongst all involved that health does suffer if housing is not right. Not just the disabled person as well, but family carers and the risks in the work place for paid care workers.

More people are having care provided at home, not just the short visit kind, but up to 24 hour coverage, which enables them to stay out of care / nursing homes. Suitable housing must be made available for this group.

Space for a wheelchair user is not a luxury it is a basic health and safety requirement.

Social Housing Providers need to do the following :-

1.       Make those needing specially adapted properties a priority as this group has very little choice to go elsewhere.
2.       Study in close detail, and case manage the disabled / older persons on their housing lists.
3.       You may not have the right housing stock. Think outside of the box where necessary to provide solutions either through new build or the adaptation of existing open market available properties.
4.       Listen carefully to the disabled as to what they need to get by, they are the experts on what it takes to get them through on a daily basis.
5.       Make sure properties are not in socially isolated areas, disabled want the same location choices as everyone else in society.
6.       Remember it will be a home but also in many cases a place of work for care workers.
7.       Stop putting wheelchair bound users on anything but the ground floor, it is not safe, even with lifts available , if cannot walk down/upstairs.  Increases evacuation time, can get stranded outside home if lift out of order. Puts unfair onus on care workers and fire department to evacuate person.

We will keep fighting on to get suitable housing for ourselves, not what someone else thinks is suitable but what we know will work well for us.


Angela 

Thursday, 15 August 2013

Commission on Residential Care - call for evidence

Dear readers for what it is worth, here are my thoughts,

Introduction.

I write this paper as the carer of a complex spinally injured Tetraplegic husband, the sister of a severely affected learning disabled adult, and the daughter of an adult with reoccurring, severe, complex mental health episodes.

Firstly to answer the specific questions posed by the commission.

The Questions.

1.       How do you define residential care?
Residential care to me is the care provided in registered care homes, nursing homes, and hospices. These places are supposed to provide round the clock appropriate support for their residents and should provide a safe and comfortable place for those that need extra support that in their particular cases living in the community could not give.
a.       Do you see extra care, retirement villages and other “housing with care” options as different by definition?
Yes, they should be but it is becoming apparent to me that because of the stigma of putting loved ones in care homes, many family members are inappropriately putting their relatives into places like this and then wondering why there are problems and sudden deteriorations in health.
b.      What makes them different?
These extra care facilities and retirement villages should be for people that need minimal care and help for daily living tasks. They should be for people that like to be part of a community feeling but still want a high degree of independence. Excellent for people who live on their own to combat loneliness, make them feel safer as people they can call on if needed. Have replaced the old warden controlled bungalows in many areas. They are totally unsuitable for people with late on set dementia, or others that need round the clock support to stay safe. The latter, because they are not usually big enough dwellings to accommodate full time care worker teams or the medical equipment that comes with complex medical conditions.

2.       What outcomes do people value when it comes to care and support?
Firstly that whatever environment a person lives in it supports them to live life to their fullest potential. That it gives the person as much choice as they can handle. Examples of, that they can choose, if appropriate to their condition, when to go to bed, get up, eat, what to wear, who to associate / socialise with, what hobbies to pursue. That the care and support provided is delivered by people trained appropriately to their need. For example people with dementia have access to specialist care-workers to help them through the different stages of the illness, people with learning difficulties have care staff that appreciate the need to constantly re enforce learning, people with a physical disability have care workers that understand the processes of SCI / MS/ MD / spina bifida / arthritis /blindness / deafness etc.

3.       Can existing residential care deliver these outcomes?
Residential care in its current form has the general reputation that the Victorian workhouses had of the past. That of somewhere no one wants to end their final days in. I believe that things will have to change or people of the next generations given a choice will refuse to use them, which cannot be a sustainable business model for the future. People’s expectations of living standards have and will continue to change. Where in the past it was quite acceptable to live in a bed sitting room arrangement with a shared bathroom / dining facilities, many would find this arrangement if fully compos mentis totally abhorrent today.  Residential care is also being used to paper over the cracks of the shortage of wheelchair accessible homes, this abuse needs to stop. Many generations now find communal living an anathema , people value their personal space, so the thought of communal sing-a-longs, being forced to associate with people they do not know, eat and live with strangers can be very frightening. The generations to come will value technology, [that technology use has changed the way we socially interact] like doing things many times on their own, will be more orientated towards their own inner circle of family and friends.
One other thing to note is that people are becoming more and more, savvy regarding medical knowledge and will not accept the poor standards of training and knowledge currently prevalent in the care sector.
So in short I believe the current model is unsustainable and will not deliver the expectations of next generations that end up needing to use such facilities.

4.       Is there a difference between good residential care and other forms of good care, if so what makes it different?
Good care where ever it is delivered should be appropriate to the individual needing that care. The persons delivering the care must be appropriately trained. The best examples of good quality care are that which is delivered by family carers because they usually actually care about the outcomes of the cared for, somehow paid care-worker companies need to “bottle this” and replicate this among their workforces. Hospices seem to also have a generally good reputation, but since their clients usually have a poor prognosis this may be the reason, or it might be because they tend to be staffed with competent specialist nursing staff.
Good care is a person centred approach that recognises that we are all different with various aspirations. That provides appropriately trained staff, that are adequately supervised. That has measures such a password protected remote web viewing so that family can see what is going on in the facility at any time as a reassurance.  Care provision that fulfils an individual’s hierarchy of needs as defined by Maslow, basic needs (e.g. physiological, safety, love, and esteem) and sometimes growth needs (self-actualization) as well or as Carl Rogers would have it that humans have one basic motive, that is the tendency to self-actualize, to fulfil one's potential and achieve the highest level of 'human-being-ness' they can.
Residential homes that provide services that actually do more than just house and feed their clients have to been seen as providing good care.

5.       How will the role of residential care change in the future?
There will always be a need for establishments that provide care that would be provided in a hospital setting if they did not exist. I cannot see how residential care can change in being anything but the place of last resort for most groups that would need to use their facilities.
It is my view that residential care should only be used in the following circumstances,
·         Where the individual’s current living arrangements would mean them coming to significant harm due to a mental incapacity.
·         Where an individual actually wants to live in a communal setting and a retirement village / extra care facility is not appropriate.
·         Where specialised end of life care is needed.
·         Where specialised respite care is needed and only if not possible to be done in own home.
Since it is the home setting of last resort in most cases, it should be made as painless a procedure as humanly possible. People should be able to have their personal possessions, some personal space, access to technology such as Satellite/Cable TV, internet, phones etc. Personal bedrooms, bathrooms, sitting space. Should be more like a high class residential hotel. In the future I can see the need for these places to have unique selling points, such as hydrotherapy pools, access to physiotherapy, specialised OT sessions etc. to make them more palatable.

6)      What future role would you like to see for residential care?
i)        #1 priority where ever possible and if the individual wants it, care should be provided in a persons’ own home.
ii)       More action needs to be taken by the government to ensure there are adequate wheelchair accessible homes available for people in the community to rent and that disability grants for people to adapt their existing homes are still supported and adequately funded.
iii)     That there is a national set of training standards and qualifications for care workers.
iv)     That care workers are considered in the same line of promotion as hospital health assistants and nursing staff, and come under the auspicious of the Royal College of Nursing in the setting of standards and codes of conduct.
v)      A national framework is developed as to the necessary levels and standards of staffing needed to look after the various conditions supported in a residential care / nursing home.
vi)     That someone is made responsible for taking an overview role of the types of care available in residential care homes large and small ensuring that they meet the spread of need in each geographical area. For example make it unacceptable for immediate
family to have to travel great distances to keep up a relationship with their LD kin.
vii)   A designated person is made responsible for ensuring that extra care and retirement villages do not house people that are inappropriate to their level of expertise.
viii)  That fire departments are stricter on the requirements for safe evacuation from shared premises housing people with particular needs, whether they be extra care facilities, retirement villages, care homes, or nursing homes.
ix)     That council planners ensure that mobility restricted individuals are not housed in buildings where they cannot be easily evacuated quickly from in an emergency. Should be a maximum time limit for evacuation like an aircraft. That building owners conform to ‘excellent’ standards of maintenance, heating, ventilation, noise control, rubbish storage and collection. 
I still firmly believe that moving into residential care will always be seen as the course of last resort for many. If the sector were developed carefully, taking into account the aspirations of the new generations, and so that no one that did not really need to be in such an establishment had choices of where to live, more people would be better accepting of the time when they became too ill / dependent to live on their own.

In summary.

Let me use my knowledge of my own family to ponder the alternatives they currently have as an example of how things have to change.

1)      My Severely Learning Disabled Brother.
My 47 year old brother has the mental capacity of a limited 2 year old having contracted TB Meningitis and epilepsy as a baby.  He lives over 60 miles away from his family in a small residential home.  The staff to care ratio is higher than some establishments, I believe it is 1 carer to 2 residents. The distance from family has severely limited the contact of family and made it impossible for me to maintain reasonable contact despite wanting to. Social services do make monthly runs to mother so that she can maintain some contact. He seems to be happy where he is, his care-workers genuinely seem to care about him. When he has not been happy in the past he has exhibited behaviour that lets us know that things are not well. Hand biting and self-harm being some examples. So well run and appropriate residential care in this case but too far away from his family.

2)      My Mother with reoccurring mental and physical health problems.
My 75 year old mother lives with her partner who also has mental health problems in a tiny one bedroomed council provided bungalow. She suffers from acute episodes of mental health illness, where she becomes totally detached from reality, becoming a danger to herself and verbally abusive to those around her. She also has mobility problems caused by the excessive weight gain caused by the mental health drugs she is on and a stomach hernia / intestine problems. She likes living independently where she is when she is well. But if you were to visit their home it is quite obvious that they are not coping well, the place is dirty and untidy. She has a visit by care worker every third day to help her shower. It is my belief that she and her partner are not supported appropriately by the social care system. They would be better living on an extra care complex, where they could socialise, people could keep an eye on them regarding their mental states and help with cooking and cleaning.     

3)      My Husband with severe and complex physical medical problems.
My 69 year old partially tetraplegic, husband and I (46) live in a two bedroom first floor flat in an extra care facility. He has passed the assessment for NHS funded continuing health care (CHC) and is supposed to have a team of care workers to look after him around the clock, enabling me in theory to return to work. We have had problems with the provision of care workers from the onset of the award of CHC. We find it incomprehensible that having passed an assessment that proves an on-going medical need we have been supplied with minimum wage under qualified care workers, that lack the capacity to take on board the complexities of his medical needs. We also live in housing that is totally unsuitable / unsafe for a full time wheelchair user. We have been put under not so subtle pressure to dissolve our marriage and place my intelligent, fully mentally aware husband into a nursing home to save the authorities money. Instead we have struggled on at home myself, putting my own physical health at risk, being used as a human hoist because of the space/ safety issues with using an electrical hoist in such a confined area. My husband becomes very down with being confined to four walls every day and longs for the private use of a small garden. We are top of the rehousing list on health grounds but since there are not the suitable specialised properties available and the lack of willingness to find us a bespoke solution to our housing problem here we sit and have done for the last three years. We are currently trying to help ourselves by engaging a philanthropic property investor consultant to buy us a bungalow for us to rent, at first with an option to buy should I get back to the full time work I dream of. We can then apply for a disability grant to make the modifications we need to make. Safety net what safety net? So in our case residential care is not wanted or welcome at this time.


Finally, slightly off piste, as it were, if more people are going to end their days in shared facilities such as residential homes. Someone is going to have to do something about the inordinate numbers of care workers that smoke. Smokers and non-smokers cannot happily co-exist.


Saturday, 13 July 2013

Wheelchair Accessible UKHousing

An essay on the plight of wheelchair bound citizens in the rental housing market.

Unfortunately people who are unable to walk and totally reliant on a wheelchair will find there are many barriers to finding somewhere to live. If you are lucky and your incapacity comes when you own your own home, you will be able to apply for a disability grant to help with making modifications to your home as long as you don’t have over the prescribed limit in savings & income.

For those without their own homes that rent to provide a roof over their heads you will encounter several difficulties. Private landlords unwilling to provide secured tenancies, and local councils / social landlords that will not take into account your particular needs. You will be left with choices all extremely unpalatable and in varying degrees unworkable.  

I write from personal experience as we have been looking for a home, rather than a roof over our heads on and off for the last 4 years.  Currently we live in a first floor, small two bedroom flat, which although it has a tiny wet room is totally unsuitable and unsafe for both my husband and his care workers. We have written to the council regarding the reasons why we need to move and they have given us a high priority for housing that just does not exist, and only allocated us 2 bedrooms which is totally unworkable for us. We need rooms of varying sizes for the following, 
  • 1 small bedroom for me to sleep in during the week so I can return to work,
  • 1 small study / changing space for care-workers,  
  • 1 small room / space to house a tilt table + all the spare equipment + charging space,
  • 1 very large (4m x 4m) master bedroom capable of taking a hospital bed that can be accessed all around + another single bed so that I can look after Hubby at the weekends during the night and maintain some intimacy in our marriage. 

We also need a large wet room + separate shower / washroom to maintain separate hygiene with the care-workers. Then open plan living / kitchen space. Barrier free front / rear access doors and interior doors wide enough to easily manoeuvre an electric wheelchair through. Outside we need somewhere safe, sheltered for Hubby to sit to make sure he gets enough daylight to maintain his vitamin D levels which is very important to his bone health.  
  
So far we have been offered two bedroom bungalows which report to be accessible which we know will be totally unsuitable and lead to us swapping our current unsafe conditions for even more problems such as
  • ·         serious infection control issues,
  • ·         rooms not big enough to allow for free access of a wheelchair,
  • ·         having to give away all our possessions to squeeze us in,
  • ·         socially isolating Hubby even more than presently,
  • ·         no storage space or room for rehabilitation equipment,
  • ·         no cognisance taken of the fact that not only a home but a place of work for full time care workers .

It is becoming increasingly apparent that no one is interested in supplying housing that is fit for purpose for disabled people. They are supposed to be grateful for anything they are offered, even if it will contribute to deterioration in their health and hastening the day they will need to move to a nursing home.

So having increasingly despaired with the social housing market I turn my sights to private rentals. We would have to contribute more to our rent as the housing benefit allowances for private are not as generous, but as I fully intend to return to work as soon as possible this is not a big issue if we can get a landlord to work with us to make a bungalow accessible. 

We came across somewhere that we could have made perfect for our circumstances, it needs some alterations but has lots of potential. We got past the first hurdle of the rental agencies that usually suddenly make the property unavailable to disabled enquirers, got to speak to the landlord to explain our situation. He seemed very understanding of our plight, I explained that we would need to change the on suite bathroom into a wet-room out of our meagre savings, then once moved in apply for a disability grant for the other changes that we needed.  That we would make changes that would not devalue his property. Also that longer term if my work situation panned out we would look to buy it off him. I also explained that we would need some sort of secured tenancy as to apply for the grant the council want to know you can live in the property for five years. Anyway we left the conversation at that point, as we had to involve the estate agent he was using to manage the rental. So I talked it through with the agent explaining the different type of rental agreement we would need, as she had no experience of other types other than the short-hold, 6 month, 12 month assured tenancies more usual in the private rental market. The estate agent and landlord subsequently had a conversation and unfortunately the landlord was not in a position to grant us a 5 years short hold or an assured tenancy so our perfect property fell through.

I have come to the realisation that this means that in most cases the private rental sector is totally unavailable to mobility restricted renters, but the local authorities / social housing associations are not providing suitable properties either, does not sound very equitable or fair to me, or looking after our most vulnerable in society, does it you?


Any ideas people how we are to find suitable housing that meets our needs.  

If is quite obvious that the local authorities do not have the expertise to deal with housing the severely mobility disabled. This leads to their housing needs being put in the too difficult basket by the housing managers leaving the disabled without suitable housing for very long periods of time. I would like to suggest a new means tested system. If the disabled person does not have assets, capital or compensation pot, that the local authorities give them a personal budget to either build or buy housing that can be adapted. With that grant being repayable on the death of the disabled person, either by handing over the house for someone else to use or by selling and repaying the grant. This would mean that the disabled could ensure that they have the housing that fits their particular circumstance rather than what the local authorities think they need. In our case we would need £200k to find a 3 bedroom bungalow that we could adapt to our needs within that budget. (175k cost + 25k adaptations ) . I know that would mean if my husband died or became too ill to live in the property I would be homeless but I could accept that if that meant he could live some where suitable.

Readers will think this too expensive, but it is only marginally more expensive than the new not fit for purpose so called accessible housing that is being currently built or actually not being built as there is a national shortage. Also there are savings in poor health outcomes that the disabled in poor housing currently suffer.

We need some out of the box thinking to help get us out of the current housing problems faced by the severely disabled. 

Sunday, 17 February 2013

Mobility Accessibility " Build it in, don't Exclude it out"

Most builders , hoteliers, landlords if you have a conversation with them about including accessibility in their building will tell you of how difficult it is, how confusing the regulations are, as an excuse as to why it does not figure on their collective radars unless confronted with a situation they can not get out of.

I know in certain situations there is a need to build to the full accessibility standards, providing the ramps , hand rails, contrasting colours, sound aids etc. and the more of this the better of course.

I would like to get people thinking of what they can do to make everyone's environment more mobility accessible and not to the exclusion of the able bodied, giving a little more choice all round.

1. Showers -
If you are going to have a separate shower and bath , why not consider making the shower a wet-room area? Wet-rooms can look very stylish / chic and if the opening wide enough allow access to a wheeled shower chair. They are easier to clean as well.

2. New build / Refurbishments -
Why not make the doors wider than the norm, it does not cost that much more, allows access to wheelchair users. Hotels easier access for those hostess trolleys, residences easier to move in with furniture.

3. Steps & ledges.
Is it really necessary to have that high lip to a patio door , that step to the front door ? Able body people will you never have a visit from a wheelchair-ed friend member of family?

4. Luxury Hotels.
You supply high end furniture to your hotels, why not investigate whether companies do stylish high-low reclining  beds. Even more luxury everyone would love.

5. Restaurants.
You supply parents with high chairs for their children, why not adjustable(height) tables for those in wheelchairs ? When buying new tables do you think about whether someone in a wheelchair can get their foot plates under the table ?

6. Carpets.
Does that carpet have to be a thick pile ? Tiles can look great, are easier to clean and allow easy pushing for wheelchair users.

7. Lifts (Elevators).
Is the lift you are building big enough to take an ambulance trolley, electric wheelchair plus attendant / carer ?  Does it have a low set mirror that allows the disabled person to see how close their feet are getting to the edge. Dual controls at a good height to allow for not being able to reach over / turn around to operate.

8. New Pool
Make one access point ramped, not all disabled people can use hoists. People love zero entry pools, they can sit in the shallows keeping cool, older people find steps difficult, severely disabled people find floating out of a wheeled pool chair a lot easier and safer.

This list could go on and on, but hopefully has been thought provoking enough to get everyone thinking about what they could do to make things a little more accessible, for EVERYONE.

look around you, while you are refurbishing / building , at what YOU can do and not at what you can't do.  



       

Monday, 4 June 2012

What could I do if we won the Euro-millions

I got to thinking what good could I do if we were the lucky winners of the enormous Euro-millions jackpot.

There is a empty plot of land opposite us, I would love to have 5 state of the art accessible bungalows built on it. I would build a little community, with a ramp accessible warm therapy pool , that the local community could use as well. Staff up the place with physiotherapists, senior experienced nurses to run the place and well paid / trained carers to help the people living there.

The spacious 2 bedroom, bungalows would be open plan so that wheelchairs have easy access everywhere. for example , ceiling hoist tracks built in. Electronic sliding front doors. Use the latest technology in Eco friendly heating and recycling of water. Make use of technology to aid those living there with their independence. The site would also have office / shower  facilities for the support staff. The gardens with shade, would be accessible, with sensory elements, raised beds etc.

if we got the business template right we would then open other sites around the country in areas where the council is failing to meet the needs of the local disabled community. I would also use the project to indulge my passions in developing business talent as I would encourage the physiotherapists to develop themselves into business units using the provided facilities to provide services to the wider community, in the spare under utilised slots for the bungalow community residents.

I would also like to fund research into new electric wheelchair battery technology, to make them last longer, maybe by some sort of recycling energy technology, plus make the batteries physically lighter and smaller. Why can't the disabled have chairs more akin to Professor Xavier's wheelchair from the X-Men.

On a personal front we would of course get Hubby the best treatment available , hire well paid / trained personal staff to help him. Buy the equipment that would make his life a lot easier, place to live, car, specially adapted electric wheelchair etc.

But at the moment no amount of money in the world would probably  be able to make him be able to walk again. 


Final thought for today : Money can do a lot of things but can not make the impossible, possible.

Thursday, 8 March 2012

Travel same old problems. Part 1.

Planning.


So you have mobility challenges , your health is a bit up and down so you cant book way in advance. If you want a hotel you will probably be okay in the bigger cities of the first world.


We wanted to stay in villa in the Orlando area, where we could do our own thing, our own washing, cook as we pleased. So I started using the web to find a suitable villa. You will find many sites listing villas with various search options. Some even report to have searches based around disability access. Buyer beware, as many owners report to have an accessible property but when you look at the limited information and photos it soon becomes apparent that their idea of accessible is that it is on one level. Forgetting that the mobility challenged still need to have a shower, use the pool and gain access to the property all of which are extremely difficult where there are steps and small enclosed showers with 4" drops and overhead shower fixings that don't allow for washing your bottom in a commode.  If you are able to book about a year in advance then there are specialist travel agencies such as http://accessibletravel.co.uk , and the handful of villas that have been made accessible to ADA standards. Be prepared to pay a lot more when using these companies. There is no equality when it comes to disability travel.  


What needs to be done:


People who run the search sites must develop and be forced to adopt proper search parameters that allow the disabled to find , easily a property that is suitable. Private owners must not be allowed to advertise as having properties that are accessible when they do not conform to any recognisable standard. 


Roll In Shower StallFurther more and more controversially I think people who own villas for sale to the general public should be made to make reasonable adjustments to their properties to allow access to all. For example Villas with more than 2 bathrooms the 3rd should have to be made into a roll in shower. Villas that are part of a resort complex should have shared access to ramps to allow access through French windows , and where no bathroom is accessible one of the available portable showers should be made available. Glenbrook Resort where we stayed did not even have a pool hoist at the clubhouse pool. This is in a country the great USA that says it is one of the best for handicap access as they call it.  



We eventually gave up and decided to try and manage especially as it was clear that the holiday company did not have a clue as to what we needed. I will be writing to their MD by the way pointing this out. http://kenwoodtravel.com and their associated company http://thetraveldirectory.com 


Equipment Hire


All I can say is shop around. We needed a shower chair prices ranged from $1000 - $200 . I want to rent it not buy it! The quality of the equipment can be a  pain in the arse, literally. We settled for mid price but still had problems with the footrests that were not big enough or safe for man sized feet, the cushion had a hole that was too big for a slender framed man as well. We had to put a cushion on top so that we could manage. Having said that I still got a snotty email back from the company at the beginning when I questioned their prices, stating they bought only quality equipment , hummmm. I don't think so. I probably could have bought a chair in better condition for $100 more at Walmart online. 


The Journey


We know that because of Hubby's particular level of disability we had to travel premium economy . So I write a detailed email to Virgin Atlantic explaining what we need. We book a meet and greet service as we cant cope with luggage and looking after getting Hubby on one of the car park buses. We used Maple Manor we do not recommend this company for disabled access as you have to meet them miles away from where you need to be, having to go up in the lift, across the terminal and then down again. There are no good spots to decamp from the vehicle where they meet you, if you transfer from a car seat to your wheelchair there is no safe place to do so. You then will have to wait in freezing cold (time of year dependant) conditions for the Gatwick assistance team. After eventually getting some help from a passing Gatwick manager we arrive at the disabled assistance corral. Warning: DO NOT RELY ON THE GATWICK STAFF TO GET YOU DOWN TO THE GATE IN GOOD TIME TO PRE BOARD. If you need to pre-board get down to the gate early (1hr +15mins prior) and make it known that it is essential that you need to pre board. We didn't, Gatwick staff came to us at 12 noon , the flight had already started boarding. Hubby had to fight his way through hundreds of others boarding then stop them while we transferred him to a special chair. Hubby then got injured as he was rammed into a cupboard in the rush to get him on board. If you are wheelchair dependant you will note with irony that the most disabled get the least help as the buggy they use is not wheelchair accessible and only for the walking wounded, not to be rude to those with lesser mobility problems. If you are totally dependant on your wheelchair you have to be pushed to the gate or roll down there yourself. The accessibility team will if you ask take your hand luggage for you. Keep your passport + boarding card with you. 


So not a good start to a long flight. Then Hubby found that the seat he had been put in , meant that he got constantly banged by passengers using the facilities and staff going up and down. We also had a cupboard door that was banged into his foot in a regular basis. The old Boeing plane used for the journey has an entertainment system that is totally unsuitable for someone with limited hand function, it being stuck in place at the seat side. By the way Virgin your food service has gone way down hill, the food is horrible. 


The assistance to get off the plane at the other end was fine if a little slow. Do not forget to tip the helper ($5 for some minimum help, $10 if a lot of help involved) or you will get cursed a tight uneducated Brit. 


Car hire 


We thought we could mange in a small people carrier so we booked with http://AVIS.com using some BA air miles left over from our trip to Australia. Big mistake the design of the car made travelling in it impossible for hubby.  I was somewhat annoyed  that when we returned the car early it was then we were informed that Avis have a special department for accessible vehicle rental. We ended renting from http://wheelchairvansofamerica.com they are very good but very expensive be prepared with insurance to pay at least $120 per day, a normal car rental would be about $50 . 


more to follow...