DISABLED ENTREPRENEUR - DISABILITY UK

Disability UK Online Health News Journal, Disability Business Directory, All-In-One Disability Business Solutions. Working in Partnership With Cymru Marketing Journal (CMJUK) & UK Website Designers

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Why Do People Assume or Presume?

July 1, 2021 / EDITOR / 2 Comments

Why Do People Assume or Presume?

Taking People For Granted, Assuming, Presuming and Mental Health.

People make assumptions as an efficient way to process the world. It is a shortcut to knowing the facts. As one Yale neurobiology professor explained, the brain’s vast neural network requires huge amounts of energy to keep it running: … One way our brain saves energy is by making assumptions. Making assumptions can ruin people’s lives.

Assume vs Presume

Presume is a verb that means to suppose, to take for granted, or to dare. Assume is a verb that means to suppose, to take for granted, to take upon, to do, or to undertake.

Assume and presume both mean “to take something for granted” or “to take something as true.” The difference between the words lies in the degree of confidence held by the speaker or writer. … ‘Presume‘ is the word to use if you’re making an informed guess based on reasonable evidence.

Therefore as an example I ask you some questions.

These are all hypothetical questions.

  1. Would you assume for example someone could find nearly $100 per month only by giving them one month’s notice for an increase in rent? Would you presume they could afford to find the $100?
  2. The second question would you assume someone who is self-employed to drop everything because you were arriving without even asking them if the date of your arrival was suitable for them? or would you presume they would just find the time because you snapped your fingers?
  3. The third question would you message a VIP and assume they have time to chat with you or that they will phone you when what you could say could have been written in an email that would take a minute or two to read, or would you expect that person to take time out of their busy schedule to hear you waffle on about something that could have been put in writing? or would you presume they would drop what they are doing to casually chat with you?
  4. Would you assume or presume that whoever you asked to call you or meet you could afford to do so? Would you assume or presume that their finances can meet the budget of an excursion for example or meeting up to go to a fancy restaurant? A self-employed person has more commitments than the average person, they have to pay the overheads of their business not just their own personal expenses.

These are all hypothetical questions that a disabled entrepreneur is faced with and I want to teach people to consider others before making rash decisions. It is unfair to put anyone on the spot regardless of their status, disability or situation.

Always discuss things and be very understanding and be respectful of someone’s wishes. Never judge based on a person’s choices.

Always find out the facts first and understand people’s circumstances before making plans or assumptions.

A self-employed person may not have the time to meet and maybe 100% dedicated to their work. “Just because you have free time or work for someone else, there is a difference. If you work for someone else your wage is guaranteed, however, if you work for yourself your income is not”.

Do take off your rose-colored tinted glasses before making plans. There is a saying “put your brain in gear before putting your mouth in motion”.

People with Rose–colored tinted glasses tend to be optimistic and have a cheerful way of looking at life. … Someone who looks at things through rose-colored tinted glasses looks on the bright side, sees the glass half full, and looks for a silver lining in all things. So their way of thinking maybe if you lose work because of a casual meet-up to not to worry as another job will come along, having a go-lucky attitude. They also may think that life is too short to worry about finances and just go with the flow and live for the moment. Their excuses will always override your thinking and you cannot win.

NEVER ASSUME OR PRESUME ANYTHING!

  1. Do not assume or presume that people can talk to you when they are working 24/7.
  2. Do not assume or presume people can meet you even for five minutes if they have a busy schedule or a critical time path and manage other people’s businesses.
  3. Do not assume or presume people can pull money out of their a##es just because you are demanding. Think about what this will do to a person’s mental state of mind if you go on your high horse and be expectant.
  4. You would not expect, assume or presume the likes of say, someone like “Elon Musk” to drop everything for you so do not think you are so special that anyone will drop everything for you.
  5. Consider the other person’s circumstances before assuming or presuming they can travel. They may have health issues and may find it difficult to travel. Do not assume or presume that someone with a physical or mental disability will recover miraculously within a short space of time of your arrival, never assume or presume anything.
  6. Never assume or presume that within a month someone can find an extra $100 per month for a rent increase when they could have lost business because of the pandemic or their job.
  7. Never invite yourself to anyone’s home without asking them first if it is convenient, do not assume or presume that you turning up someone will drop everything for you.

“It really rattles me when people are so narrow-minded and do not care about anything apart from themselves”.

People simply do not care: https://disabledentrepreneur.uk/why-people-do-not-care

I am venting my anger because not only do I have time wasters trying to waste my precious time, attempting me to do work but refusing to sign contracts, I also have those that think they can waste my precious money.

If you cannot support me, why bother talking to me? If you are just wanting to meet up to be nosey and judgemental, you can read about me online and do not have to see me? https://renataentrepreneur.com/irenata-my-sites

Do take people’s circumstances into consideration especially if they are running a business and have health issues.

If you want to see someone but they are not comfortable meeting you consider Facetime, Skype, Zoom, Teams to name a few, I personally do not have to see you in person.

Do not assume or presume that I for one will drop everything for you because you are arriving, you should never put anyone on the spot and expect to meet if you know they have health issues.

Do not assume or presume that my health issues will miraculously go away within a short space of time when I personally have battled my illness for 30 years. Do not put people on the spot and force them into a situation they do not want to be in.

Do not be selfish.

Do not assume or presume because you are turning up on a weekend that someone such as myself does not work weekends. Always find out the facts and give the other person plenty of time to make adjustments if at all possible and discuss a happy medium where both parties can agree to something, consider the person’s disabilities, and do not expect too much from that person if you care about them.

Ask in advance if that particular date is suitable for both parties concerned, do not assume or presume that they can take time off work, and be aware that may lose business because of your selfish, careless thinking.

Life lesson does not matter how old you are, if you want something from someone be prepared to compensate them for their time, service, and resources.

Never assume or presume people’s financial circumstances or their health and never assume or presume to take up people’s time.

Assumption can lead to resentment and animosity. Always communicate properly and understand that people that run small businesses may not have free time especially if they are trying to build their empires. Always consider other people’s circumstances first before being selfish.

There are so many self-centered people in this world, that simply only care about themselves but live a lie pretending they care about others, do not be one of them!

Note From the Editor.

Putting my health issues aside for a moment, I run several businesses www.irenata.com, and manage over 100 websites. I support startups that may not have the money to pay for a website upfront but want a helping hand to get them started. In return, they recommend me to other businesses. Just because I have over 100 websites they may not all be payable until the end of the trial period. Where I have to dedicate at least 2-4 hours of work a month to each website, so do the maths, that is 2-4 x hours per website x 100 websites = 200 – 400 hours per month divided by 4 weeks is 50 -100 hours a week which divided by 7 days is 7-14 hours per day without me doing anything else, so where have I find the time to meet up for a casual chit chat? I don’t and I can’t. I am not going to jeopardize my business for anyone.

This Is How My Critical Time Path Should Look Like below:

However, I cannot keep to my plan and most certainly cannot take time off work.

This is just an example CTP.

“So before assuming or presuming I can take time off work, take into consideration that I run several businesses of my own and manage other people’s businesses also”, so do the maths.

So before being judgemental and labeling me, I will protect my business with my life and will put it before anyone and anything else. I know there are people who are just watching and waiting for me to fail but I will not let that happen.

“Just because I have a disability does not make me crazy”.

If I choose not to waste my time walking around a park aimlessly for 10 minutes a day that’s my business. If I want fresh air I can step outside or if I want to do exercise I can do it in the comfort of my home.

I can manage my disabilities using my own methodology and do not like people trying to change my way of thinking unless I specifically ask them to.

If you have not walked in my shoes you have no right to make opinions, assumptions, or presumptions.

#assume #assuming #presume #presuming #takingforgranted

Personal Experience with claiming (PIP)

May 2, 2021 / EDITOR / 3 Comments
PERSONAL INDEPENDANCE PAYMENT

When does reform become dangerous?

Over three years ago the Conservatives began to roll out personal independence payments (PIP) – in essence, the mandatory, mass re-testing of disabled and chronically ill people – and the answer is getting stark.

Are you entitled to Personal Independance Payment?

You can appeal by writing an in-depth letter and collecting all the evidence to help with your claim. My evidence is my online journal on this site which I own.


Personal independence payments assessment is designed to punish the poor and ill, regardless if it is a legitimate claim or not. Everyone is thrown into one basket.

A report released by the Muscular Dystrophy UK is the latest piece of evidence to expose an administrative catastrophe: appointments canceled at the last minute, lost applications, year-long delays.

Two in five respondents report being sent to an assessment centre that wasn’t accessible for disabled people. This is designed purposely to save the government money as the people that genuinely want help may give up in the process of fighting back. Not everyone knows how to appeal and if the government makes it hard for them to claim and appeal, the disabled person will just simply just give up. The assement is designed to break you down.

Since the pandemic interviews have been suspended but prior to the lockdown and my own personal experience once you manage to make it inside the building, the picture is as dire: widespread reports of assessors – employed by private firms hired by the Department for Work and Pensions – who showed no respect for disabled people, (this is especially true in my case and the humiliation I personally felt and the length of time I had to stand ), while some didn’t even understand the condition they were testing (one man, with muscular dystrophy, pointed out that the word “progressive” means “muscles don’t come back”).

Once you are at the interview you will be asked to answer a series of questions and perform endurance manoeuvers to see if you can balance on your feet, walk or how mobile you are etc. My daughter’s neurologist wrote in his report my daughter has a spastic gate and the assessor undermined the neurologist report saying my daughter could walk fine.

You will also be asked questions about your finances and if you are coping or if you are in rent arrears and credit card debt to mental health issues. I was asked what I do for a living and did not elaborate on it other than to say I do web design.

I think this form of questioning is to intimidate and degrade you.

Just because one can manage finances does not make you a healthy person. Even if you spend 60 hours or more on the internet working as some entrepreneurs do will not make that person any less disabled.

Even if the person who is an entrepreneur but disabled could successfully trade online would not mean that because they are successful at what they do that there is nothing wrong with them.

I just have a problem with interacting physically and germ contamination, I have no problem being online.

I was personally asked about my toilet hygiene and routine and if I sat on the toilet and how I wiped my you know what and how I maneuvered around in the bathroom. I felt humiliated and felt the whole ordeal very upsetting and I still have anxiety about it to this day. So you can imagine my fear and anxiety of another assessment next year.

One woman, with a muscle-wasting disease, said that she developed panic attacks after her assessment. She is now under the care of a mental health team and doesn’t leave her house.

That the government deliberately built PIP with tightened criteria – and is sitting by as the system descends into disarray – becomes grimmer still when you consider that this is being done to a benefit tied to other essential disability services that people cannot live without.

Without PIP a disabled person can’t access anything from carer’s allowance to severe disability premium. If that isn’t enough, anyone who is rejected – or bumped down to the standard rate – is also barred from the Motability scheme for an accessible car or powered wheelchair.

Sarah, a nurse with progressive muscle wasting and weakness, was seven months pregnant – and was forced to hand back her Motability car. The 29-year-old had been receiving the higher rate of disability living allowance (the predecessor to PIP), but after being reassessed she was knocked down to the standard rate – despite her condition deteriorating.

Sarah could not take her fatigue medicine without affecting her pregnancy, and her disability meant she was at risk of falling when she walksed, and permanent damage. “That vehicle was a lifeline to me,” she says. “I’ve lost my independence.”

Sarah appealed and was due at a tribunal but found it was canceled with just two days’ notice – and no explanation.


The government is skewing benefits appeals against disabled people.

It took the resignation of Iain Duncan Smith and a budget hole of billions to get the mainstream media to shine a light on the disaster of PIP – or many politicians to find a conscience. One cut to the benefit is stopped. A new secretary of state is hired. And the news cycle moves on. The disabled can’t. For many, things are only getting worse.

Between 400 and 500 adapted cars, powered wheelchairs, and scooters are being taken away from disabled people every week. Independence went – with a maximum of seven weeks to hand your lifeline back. As an insight into the logic, let alone empathy, in this system, that’s notably less time than it takes to go to appeal or even to get the results of mandatory reconsideration – meaning the DWP’s ruling can be overturned, but the disabled person’s car or wheelchair will already have been taken. (At the last count, 60% of appeals against PIP were successful).

Darran uses a wheelchair – and has a degenerative muscle wasting disease – but last year was downgraded on PIP and lost his car. In his own words, it left him “housebound and isolated”, and he scraped together the deposit for another accessible vehicle. The DWP later informed Darran that its decision had been “mistaken”, and his old car would be returned. “My £2,000 deposit is non-refundable,” he says. “I’ve lost that money.”

This is starting to look like a game played by the ‘Dr. Evil’s’ of this world with repercussions on ordinary disabled people’s lives. Take away benefits and the sick become destitute. Remove a car or wheelchair and disabled people become housebound. It’s happening right now – and what’s worse, most of the public won’t even know it, not unless people fight for their rights and have advocates speaking on their behalf.

Note From the Editor.

For me I have severe OCD I cannot be around people and my symptoms have only got worse since the pandemic.

“I am paranoid about germs“.

I even registered a domain name www.germawareness.co.uk as I think Saliva, Postal System, and Cross Contamination play an important role in spreading germs.

I also have severe depression and the only way I manage is if I self isolate. The only person I can be around is my daughter and she too is disabled with MS.

I can understand why the government has put a tight reign on the benefit and that is to stop people scamming the system. I know of one person personally, that would walk with a walking stick for show but when he was drunk he could walk perfectly normally. The government needs to send out spies on scammers that claim to have bad backs but go grocery shopping when they think no one is looking.

I am the modern-day female version of ‘Howard Hughes’ he suffered from severe OCD and self-isolated.

“I can function to a certain degree, but only in my own quarantined environment and if I have surplus disposable gloves and litres of Dettol Disinfectant on hand if I have intrusive thoughts and my OCD is playing up. I also have a designated area no one can enter or touch”.

I used to be able to venture out but now I have anxiety and panic attacks at the sheer thought of seeing other people. I am fine online but physically is a no-no for me. I used to enjoy going out with my daughter once a month when she had her monthly blood and urine tests done but that all stopped not only because my OCD has worsened but because the hospital has strict rules and that the patient should come in on their own unless they are severely disabled.

Obviously, if my daughter needed urgent emergency assistance outside of my home I would have to bite the bullet and no doubt in my mind burn all my clothing when I came home. My daughter’s being is a high priority to me so I would have to sacrifice my own just to help her, knowing I had a counteracting measure in place to ease my anxiety but that would be in exceptional circumstances.

I remember when I had my last assessment and the assessor claimed there was nothing wrong with me. She insisted on touching my photo ID even though I told her I had OCD and I had to stand for one and half hours as I did not want to sit down on public seating (This is humiliation, discrimination and if it causes harm under duress is also against the human rights act).

She also asked me if I had any suicidal thoughts, well in my opinion that is like handing someone a loaded gun. You simply do not put those thoughts into someone’s head if they say they have severe depression. Whatever is in the medical notes should suffice and some unqualified assessor should not plant a seed into someone’s head. Even if I had suicidal thoughts I would not admit to them, not that I have had, just saying.

(I have a reason to live and hopefully, there may be a cure for my OCD someday). I have set goals and am doing my best to achieve them.

But for someone more vulnerable than myself this is highly unprofessional to ask about suicide.

(I should have recorded the interview).

Imagine the applicant going home after the interview and then attempting their own life all because the assessor gave them the idea.

My assessment is up for renewal next year and there is no way I am going to go as I cannot venture out because of my mental health. I also found out that the DWP Agency Capita employs school leavers who have no professional qualifications. I know this as a fact as my daughter as it happens, knows one of them and they are really good friends. The other thing is this particular person actually spoke about people she had assessed to my daughter.

One can obviously see I am stressing about it a year ahead of my time but if I had enough money and I would not depend on PIP to help me buy disposable gloves and disinfectant at alarming levels.

https://www.theguardian.com/commentisfree/2016/jun/07/pip-disaster-disabled-access-report-benefits

https://www.independent.co.uk/news/uk/home-news/philippa-day-inquest-dwp-overdose-benefits-b1793424.html

Atos pays out for negligent PIP assessment after visit from debt enforcement officers

#personalindependancepayment #pip #disabilityallowance #mobilityallowance #tribunals #pipassessment #pipassessor #capita

Coping With Mental Health As An Entrepreneur

March 31, 2021 / EDITOR / 0 Comments

I have not been on this site for a while now as I have been working mainly on my other sites www.ukwebsitedesigners.co.uk and https://marketingagency.cymrumarketing.com/#home I have forwarded the domain name www.cymrumarketing.co.uk to this sub domain but it does not always work with Norton or Firewalls for some reason.

I have also updated the Disclaimer Page & added a Networking Page under the heading Legal Pages, this is to let viewers know that the owner of this site uses a SEO Link Wheels to generate traffic and that all the Websites and Blogs are all under one umbrella belonging to Renata M Barnes (UK Website Designers) You will see the credit in the footer of all the websites I own and also manage for other clients.

Moving on I have also started to intergrate video marketing into my services. This is a useful tool to attract business and I am now offering it to my clients. You can view a the portfolio of Videos here.

As for my health it is starting to deteriorate as the pressures and daily stresses of life can sometimes be overwhelming. I am fighting hard for it not to beat me but when my own health professionals are working against me rather than for me it can be too much to bear…….I will explain.

Not only am I disabled I also have a disabled daughter that I am officially a carer for, so when I see red flags I tend to question things as in the case of my GP who threatens you if you make waves. Read the latest on this Surgery that has brought me to breaking point: https://marketingagency.cymrumarketing.com/category/bayer-pharmaceutical/ All I was doing was voicing my concerns as my daughter is classed as a vulnerable person and I was told I lack respect to the highly qualified pharmacist and clinician at the surgery and was told that seeing there is a breakdown of doctor/patient relationship it would be in my best interest to find another surgery.

“I am really struggling with my health and have developed social disconnection disorder and have a fear of venturing out. The less face to face human interaction I have, the happier I feel”. I have been hurt too many times to care to mention and the people I trusted the most betrayed me. In my lifetime I have experienced discrimination, racial attacks, have been abused physically and mentally and have been physically assaulted, disrespected, undermined, critised, judged, belittled, robbed, have felt sadness, dispair and dealt with grief. All these things are contributing factors to my mental disability, which has been caused by other people and entities. There is no denying my mental health is due to a domino effect caused by direct consequences to other peoples actions.

My Richter Mental Health Scale.

It is because of certain individuals and certain events that I am this way. I am 58 yrs old and have met my fair share of people over the years and I can count on my one hand how many people I can trust. I can also name each and every single person and entity responsible for my ill health and the reasons why.

Some cope by turning to drinking alcohol or taking recreational drugs. People smoke cigarettes claiming it calms their nerves, I do not smoke cigarettes, do not drink alcohol or take recreational drugs but depend on the prescription medication that are prescribed for me. Everyone has different ways with coping with stress, trauma and life events, mine is documenting everything (therapeutic) and adapting around my disabilities aswell as trying to help others.

Anaphylaxis Allergy.

I also cancelled my Covid-19 Vaccine appointment as I have a severe anaphylaxis allergy to PEG where I was vaccinated with steriod in the past which had polythylene glycol in fact over the years I have had many anaphlaxis allergies including severe breathing difficulties from penicillin and severe skin allergy where my face looked reptilian and I was in excrutiating pain, all of which is on my medical records. https://marketingagency.cymrumarketing.com/2021/03/19/polyethylene-glycol-peg-allergy-as-a-cause-of-anaphylaxis/ I am not prepared to take any risks with my life or become more ill than I already am. At least with my OCD, Depression I can manage my life to a certain degree and can work around my disabilities. But being off work fully is inconceivable and is something I cannot do as I have obligations to my clients.

I have to be online every single day, imagine being too ill to work what would happen to your business if you had no one to help you? Your clients are not going to say “ok call us when you feel better”, the food chain still has to carry on. I have heard the second vaccine is worse the the first but I am waiting on herd immunity to kick in as I do not plan venturing out any time soon.

I would not describe myself as a hypochondriac as all my disabilities are medically documented. I try not to think about illnesses unless it is affecting me directly and at any given time. I try to actually block out my disabilities and try to live a relatively normal life to a certain degree (although there is nothing normal about me). The world on the internet is not going to know about my disabilities unless they bother to do some research about me, so me sitting in front of a computer screen I am as normal as the next person.

I cannot be critised for having no empathy. I will help people in need but will never make it personal. If someone needs me to lend them my ear or a shoulder I will try and help.

To be frank I have coped better than most during the Covid-19 Lockdown. My business has improved as people have turned to the internet for a second income stream. Where I had issues about people bumping into you and not looking where they where going in the past, it is as if the heavens have opened up and had everyone stay 2 metres apart (not that I go out anywhere though).

Wearing disposable latex gloves is no longer questionable and I do not feel the odd one out anymore.

I do miss going out once a month with my daughter when she and I used to go up to the hospital for her to have her monthly blood done and then we would go to a restaurant in the city centre. I won’t say I will never go again as they say “never say never”, but it is going to take me a long time to adjust to the new surroundings and facing people at the moment is really causing me distress. I am fine with the grocery and courier drivers but that is as far as I am willing to interact physically with other people other than my family.

“I do have a goal and that is to make enough money for me to retire comfortably and for my daughter to have a head start in life. My priority is my family and my business and nothing else”.

I won’t let this general practice surgery beat me. I have a long list of people I can complain to.

Coping With Mental Health in General.

  1. Take time out to have some TLC. Do something that will make you happy and relaxed. Try to occupy you mond with something else other than what is worrying you.
  2. If you work for a company see if they have an HR department that deals with mental health. If not suggest that they do have a department and volunteer to be a spokesperson, you will no longer be seen as a follower and more so as a leader. Every business no matter how big or small should have some sort of department to air your worries and anxieties and perhaps meet up once a week to just chat. However if you find that there is no such option and you have had no alternative to tell your employer, he/she has a responsibility under Equalities Act to be obliging and to accommodate you and your condition if it is considered a long term affliction. You may not be the only one that is suffering so considering starting a club even after work can make all the difference.
  3. Stay focused it is easy to just to clock watch until the hour hand hits 5 o’clock but that does not help you or your employer hence you need to set goals and try to make some progress on a daily basis. You should concentrate on the work in hand but at the same time consider starting a second income stream and do research and learn. Reading helps people to stay motivated and empowers them to learn a new skill. This skill could help your employer or can help you to break away and go it alone.
  4. Do not over critisie yourself, if things are not going your way, tomorrow is another day. Accepting the fact that we all experience good days and bad days is just a way of life and we need to learn to overcome obstacles that come our way. For me venting my anxiety, anger and frustration online is therapeutical. I know some one will read it and will relate. I also think that what I write could actually help someone other than myself.
  5. The impact of problems such as depression and anxiety are unique and individual to each and every one of us and how we cope with them and different situations of life is equally as individual. Above I have merely mentioned some advice on dealing with issues of mental health in the workplace, but speaking to your GP and building a network of support are arguably the most important steps you can take in your recovery. For me I personally will not be relating my anxieties any time soon to my GP if I still have one, as it is practice management that you tell the reception first what is wrong with you, what ever happend to GDPR and not sharing the information with anyone other than your doctor. According to an inspection report that I downloaded on another post I made https://marketingagency.cymrumarketing.com/2021/03/30/gp-surgeries-are-small-businesses/ the receptionists have to sign a non disclosure agreement. This is hog wash if they wish to talk about you without actually mentioning you name.

Super Power.

Disabled Entrepreneur Super Power!

Just because I have a mental health disability does not make me less of a person. My disability does not define me and make me less intelligent, in fact on the contrary my disability is my ‘Super Power’ and although it comes with challenges it gives me strength and purpose to carry on and help motivate and empower others that having a disability is not the end of the world and you can still achieve your aspirations and all you need is a gentle push. Never let some tell you it cannot be done or it is impossible for you to achieve, listen to your heart and not what others tell you. Do not listen to naysayers.

My Super Power is everytime anyone disrespects me, tries to undermined me or do other atrocities I will write about them. Anyone throwing obstactles in my way, making my life difficult or miserable, I will document. Everytime anyone tries to do anything to hurt me I will hit the keyboard. The same goes if I see anyone being treated unfairly, the perpetrator will feel my Super Power.

Whats your super power? Mine is exercising my journalist skills!

Reaching Out.

If you want to talk to just drop me a line, I am happy to chat to you online or send emails. Although I do not do face to face meetings I am happy to help anyone who is feeling distressed. Just because I have difficulty interacting physically does not mean I have a problem interacting virtually. Remember a problem shared is a problem halved. If you have a network of people you can rely on then that is fine, but if you don’t there are many organisation out there that can help and I also can lend an ear or shoulder to cry on or send virtual hugs.

Royal Mail VS Other Couriers & People With Disabilities.

January 16, 2021 / G0LDEND0MA1NS / 1 Comment

Royal Mail Vs Courier & People With Disabilities.

This post is a mixture of two posts rolled into one (no pun intended).

  1. The First Being Logistics.
  2. The Second About Disabilities.

History of Royal Mail was originally established in 1516 as a department by the Royal Family. The company’s subsidiary company Royal Mail Group Limited operates the brands Royal Mail (letters) and Parcelforce Worldwide (parcels).

The company provides mail collection and delivery services throughout the UK and is now a private company after it’s shares where floated on the stock exchange in 2015.

https://en.wikipedia.org/wiki/Royal_Mail

GRIEVANCE

Now my grievance is that such a big company has no online chat and if one wanted to lodge a complaint this is what they say “We are currently experiencing very high call volumes”, this tells me their service is not up to scratch and they have not employed enough people to deal with the demand and are delivering poor service. The response time is between 10 and 35 days.

For people with mental health and immune disorders, this is absolutely unacceptable.

Employ more staff or give up your yearly bonuses and have a cut in salary meaning salaries from the top and that way you will be able to afford to employ more people.

Just because you are a PLC company there have been many before you which have tried and failed in our current climate with businesses going bust left right and centre.

You have to stay ahead of your competion, you need to dig deep into your pockets to survive.

Furthermore their website is not straight forward to navigate and I should know as I build websites.

“There should be no room for error”.

Any decent company should have online chat.

So this is the domino effect of a company simply not doing their jobs properly as I will explain:

Two parcels were sent on 12/01/21 from the same Royal Mail Post Office, one to ‘Amazon’ and the other to ‘Pretty Little Thing’. The Amazon notification came within 24 hours and refund within 48 hours but for ‘Pretty Little Thing’ the parcel is still in the sorting office even though ‘Royal Mail’ aims to deliver in one working day.

Now considering there is a time frame for when things can be returned and my daughter’s return date is bordering on the deadline, you would think they would speed things along.

My daughter who suffers with Multiple Scleroris is on the verge of having a relapse because of ‘Royal Mail’.

Multiple Sclerosis can leave a person wheelchair or bed bound, so as her carer I think it is only right to ruffle a few feathers.

To think before Christmas someone refused to use Royal Mail to send a fragile gift and I tried defending the company I now have egg on my face, and so has my daughter.

Unless the company can up with a quick plan of action I will not be saying a good word about this company.

The CEO is Stuart Simpson.

Disability Discrimination

October 10, 2020 / EDITOR / 1 Comment
Disability Discrimination

Disability Discrimination.

Disability Discrimination is rife especailly if you do not look disabled.

People can draw conclusions without actually looking at the facts and whether it is discrimination in the workplace or an airport people with disabilities have rights and should not be humiliated.

Companies should not pass the buck and should own up to their misdoings and compensate the person they have discriminated against.

Far too often untrained staff can cast judgment and make a disabled person feel degraded and made to look like they are liars when in reality some disabilities are silent.

People with autoimmune disorders for example may not necessarily look disabled at a glance. The same applies to people with mental health conditions.

I think everyone who is disabled and diagnosed by a doctor, consultant, or professor should carry a disabled card. Not everyone wears a neon sign on their forehead saying they are disabled.

I remember from personal experience refusing to step barefoot on airport flooring whilst I was told to remove my shoes and the looks I was being given as I was holding everyone up was beyond belief. I was then given used plastic shoe covers to cover my feet.

Had I continued making a fuss I would most probably have been ushered away or refused to go through customs and consequently missing my flight. I had to just bite my tongue and reason with myself that the cross-contamination of germs providing they did not get into my bloodstream could be washed away as soon as I came home.

This was very distressing and for the two and half hour flight plus the one-hour drive home felt like it was taking forever and felt like hell as I could not wait to wash my feet.

Not that I plan to go anywhere any time soon but the next time I plan to travel by air I will be prepared and will have my own shoe protector coverings.

On another occasion, just before a court hearing where I was appearing as a witness, I was told I could not bring my hand sanitizer past the security gate. You can imagine the commotion I caused whilst solicitors, judges, and barristers were trying to get past to the courtrooms, in the end, they let me through.

Discrimination is not just for disabled people it can range from, religion, race, gender and age, and sexual orientation. Discrimination is the act of judging someone based on the groups, classes, or other categories to which they are perceived to belong to.

Some links to disabled discrimination news:

https://www.independent.co.uk/travel/news-and-advice/disabled-woman-stansted-airport-refuse-help-ryanair-nathalie-allport-grantham-a8138051.html

https://www.theguardian.com/uk-news/2019/oct/29/met-treatment-of-disabled-xr-activists-branded-degrading-and-humiliating

Coronavirus: Government’s failure to offer video PIP appeals ‘is discrimination’
Watchdog ‘could finally be set to launch benefit deaths inquiry’

https://www.skillcast.com/blog/12-notorious-uk-discrimination-cases

My recommendation including shoes coverings and disability aids.

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