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A Theory on Why Car Insurance Premiums Are on The Rise

As many motorists will have noticed recently insurance premiums have risen astronomically and many are asking why.

I have a theory.

In 2010, while driving to the shop one wintery evening I came to a junction controlled by traffic lights, and my light was red so I obviously stopped. To my left a Morrisons truck also stopped. On getting a green light, I pulled forward a bit as I was turning right and traffic coming the other way had priority. The Morrisons truck to my left started turning left, and the trailer hit an icy patch and slid into the side of my car, destroying the nearside wing mirror and leaving scratches and scrapes on the front passenger door.

Next day I called the insurance company, gave them the details of what had happened, they advised that not only did they cover me but coincidentally they also covered the Morrisons fleet as well. That same day they had a replacement car out to me and collected my car to be repaired. The place that would be doing the repairs took it on a flatbed truck.

A couple of weeks later my car was returned to me with the repairs having been done. The replacement car was taken away and it was all done and dusted.

Cut to 13 years later and compare that experience with my latest one after a minor accident. Driving from my home in Scotland to my Mum and Stepdad’s in Wales, I stopped off at Todhills rest area on the M6 for a coffee. On leaving the area I began to accelerate down the slip road to rejoin the motorway when a truck driver in front decided to stop his truck, on the slip road, open his cab door in order to empty his coffee or tea mug outside. I’d moved over to pass him when the bottom corner of his door made contact with my car, hitting it just below roof level, denting the A pillar and the front passenger door, shattering the glass in that door, leaving paint on the B and C pillars and leaving gouges out of the rear quarter glass.

By this point I was almost back on the motorway so it wouldn’t have been safe to stop, I had to keep going. When I got to Wales I could get out and see the extent of the damage. Again I called the insurance company that same day and gave them the details. They had a hire car out to me the next day and said they’d arrange for a repairer to collect my car from my home and get it repaired.

So I waited. And then I waited some more. And more. After 4 weeks a company called Motor Repair Network, (MRN) contacted me to arrange to collect my car and said they had a repairer in Glasgow who would do the required work. This repairer was called Activate Accident Repair, (AAR) but my next call didn’t come from them. It came from yet another company called Glasgow Recovery who announced they’d actually been given the task of collecting the car and taking it to Glasgow, to the actual company who would be doing the repairs.

Once the car got to AAR they sent me a link to an online portal where they said I could keep updated on the progress of the repairs, so I watched as it went through assessment, estimated cost, approval from the insurance and then a status of repairs completed. I waited a few days after this status had appeared and then contacted what I thought was the repair company AAR, through their own portal, but it was MRN who responded stating that the repairs had been completed, but that the repairer was awaiting parts which were on back order. So, the repairs are complete, meaning finished, done, finito. But they’re waiting for parts. Parts needed to carry out the repairs. The repairs which are completed. Hmmm.

3 weeks after the status repairs completed had appeared on the portal I got a call from the actual repairers AAR asking if it would be OK to bring my car back that afternoon, which was fine by me as you can probably imagine.

From start to finish the repairs to what was really minor damage had taken almost exactly 3 monthsand involved input from the insurance, the broker or whatever they are, this Motor Repair Network, a recovery company and the actual repairers themselves Activate Accident Repair. 4 companies to do what 2 had been able to do some 13 years prior. And each one of those companies would have needed payment for their part of the job.

Coincidentally, both cars were Peugeot 3008s and both had been damaged by trucks.

Space Invaders

This post, from the blog diary of a disabled person, explains what happens when people use spaces designed for disabled people.

Space Invaders.

How the cost of living crisis is hurting disabled people

The cost of living crisis is affecting everyone in the UK, but especially disabled people. Disabled people face extra costs of £975 a month on average to reach the same living standards as non-disabled people. These costs include things like specialised equipment, adaptations, transport, care and support.

But now, disabled people are also facing soaring energy bills, rising food prices and inflation. This is putting them under immense financial pressure and forcing them to make impossible choices between essentials.

The energy crisis and disabled people

One of the main challenges for disabled people is the energy crisis. Many disabled people need to use more energy because of their impairment or condition. For example, they may need to keep their home at a certain temperature, use electric appliances like wheelchairs or hoists, or charge medical devices like ventilators or nebulisers.

According to Scope, a disability charity, over a third of disabled adults feel that their impairment or condition has an impact on how much energy they use. And 91% of them are worried about energy bills this winter.

But the government’s support for disabled people to cope with the energy crisis is not enough. The Warm Home Discount, which gives eligible households a £150 rebate on their electricity bill, does not cover the extra costs that disabled people face. And the Disability Cost of Living Payment, which gave some disabled people a one-off payment of £150, comes nowhere near the costs. Just as an example, I’m currently paying over £200 per month for gas and electricity.

Scope’s research shows that 80% of disabled people receiving the £150 cost of living payment said it would not be enough to cover their increased costs for essentials. And 57% of disabled people eligible for the £650 cost of living payment said it would not be enough either.

As a result, many disabled people are falling into debt or cutting back on other essentials to pay their energy bills. Scope’s figures show that almost a third of disabled people have been pushed into debt in the last year, compared to 16% of non-disabled people. And last month, the average energy debt of disabled households supported by Scope increased to £1,794.

The impact on disabled people’s health and wellbeing

The cost of living crisis is not only affecting disabled people’s finances, but also their health and wellbeing. Many disabled people are having to sacrifice their basic needs and dignity to cope with the rising costs.

Scope’s survey reveals some of the shocking choices that disabled people are making because of the cost of living crisis:

  • 38% of disabled people said they were not using heating when cold because of the cost of living, compared to 26% of non-disabled adults
  • 34% of disabled people said they were buying lower quality food, skipping meals and/or eating less because of the cost of living, compared to 19% of non-disabled adults
  • 20% of disabled people said they were cutting back or stopping showering and bathing because of the cost of living, compared to 9% of non-disabled adults

These choices can have serious consequences for disabled people’s physical and mental health. For example, not heating their home can increase the risk of infections, respiratory problems or hypothermia. Not eating enough or well can affect their immune system, energy levels or medication effectiveness. And not showering or bathing can lead to skin infections, pressure sores or loss of self-esteem.

What needs to change?

The cost of living crisis is making disabled people’s lives harder and more miserable. They deserve better support from the government and the energy sector to meet their needs and live with dignity.

Scope is calling on the government to:

Scope is also urging the energy regulators and suppliers to:

  • Extend the Warm Home Discount to more disabled customers who are struggling with their energy bills. Scope says that the current eligibility criteria are too narrow and exclude many disabled people who need the support.
  • Provide clear and accessible information and advice to disabled customers on how to switch to cheaper tariffs, access grants or schemes, or improve their energy efficiency. Scope says that many disabled people are not aware of their options or find it difficult to access them due to communication barriers or digital exclusion.
  • Offer flexible and fair payment plans to disabled customers who are in debt or arrears. Scope says that many disabled people are facing aggressive debt collection practices or threats of disconnection from their energy suppliers. Scope says that energy suppliers should take into account disabled people’s circumstances and income when setting up repayment arrangements.

How you can help

If you are a disabled person or know someone who is, you can get help from Scope’s Disability Energy Support service. This is a free and confidential service that can help you with your energy bills, debt, switching, grants and more. You can contact them by phone, email or webchat.

You can also support Scope’s campaign for a fairer deal for disabled people by signing their petition, sharing your story, or donating to their work.

Together, we can make sure that disabled people are not left behind in the cost of living crisis. We deserve to live with dignity, equality and independence.

Urinary catheters: what they are and how they can help

Urinary catheters are flexible tubes that are used to drain the bladder and collect urine in a drainage bag or a valve. They can be inserted through the urethra (the tube that carries urine out of the body) or through a small opening in the lower abdomen (the tummy). Urinary catheters are usually inserted by doctors or nurses in hospital or in the community.

There are different types of urinary catheters, depending on how long they are needed and how they are inserted. The main types are:

I have a Supra-Pubic Catheter. This is a tube that is inserted into a hole in my lower abdomen, just beneath my belly button, and directly into my bladder. I had the surgery for this in May 2018 after approximately 10 years of self-catheterising, which is inserting a tube into the urethra and into the bladder several times per day in order to drain the bladder. My hands got too unsteady to do this without causing significant pain and trauma. I made the decision to have surgery for an SPC and I’ve never looked back. Every 8 weeks a district nurse calls by my home to change the catheter.

Urinary catheters can have various benefits for people who have difficulty peeing naturally. They can:

However, urinary catheters can also have some risks and challenges, such as:

To reduce the risks and challenges of using urinary catheters, you should follow some general advice:

Urinary catheters are flexible tubes that are used to drain the bladder and collect urine in a drainage bag or a valve. They can be inserted through the urethra or through a small opening in the lower abdomen. There are different types of urinary catheters, depending on how long they are needed and how they are inserted. Urinary catheters can have various benefits for people who have difficulty peeing naturally, but they can also have some risks and challenges. To reduce these, you should choose the right type of catheter for your needs and preferences, keep your catheter clean and well-maintained, drink plenty of fluids, and seek support if you need it.

Using hearing aids: tips and advice

Hearing aids are small devices that fit in or behind your ear and can help you to hear sound louder and more clearly. They are battery-operated and have a microphone that picks up the sounds around you. These sounds are processed and amplified electronically, passed on to a receiver and converted back into sounds that you can hear.

Hearing aids can improve your quality of life by helping you to communicate, enjoy social activities, and stay safe and independent. However, they may also require some adjustment and maintenance to get the best results. Here are some tips and advice on using hearing aids:

Using hearing aids can help you hear better and improve your quality of life. However, they may also require some adjustment and maintenance to get the best results. By following these tips and advice on using hearing aids, you can make the most of your hearing experience.

What is Sensorineural Deafness and how does it affect people?

Because of my MS, in 2017 I found I was struggling with hearing.  Specifically, in hearing people speaking to me in noisy environments and not being able to hear people speaking to me if I wasn’t facing them.  I also found I’ve been lipreading for a number of years without even being aware of it.

Sensorineural deafness, also known as sensorineural hearing loss (SNHL), is a type of hearing loss that affects the inner ear or the nerve pathways that carry sound signals to the brain. It is the most common cause of permanent hearing loss in adults, accounting for more than 90% of cases.

Sensorineural deafness can have various causes, such as:

In my case the reason for my deafness was nerve damage caused by my MS.

Sensorineural deafness can affect one or both ears and can range from mild to profound. It can also affect different frequencies of sound differently. People with sensorineural deafness may experience:

  • Difficulty hearing soft or distant sounds
  • Difficulty understanding speech in noisy environments
  • Difficulty hearing high-pitched sounds, such as children’s voices or birdsong
  • Tinnitus: a ringing, buzzing, hissing, or humming sound in the ears
  • Vertigo: a sensation of spinning or losing balance
  • Hyperacusis: an increased sensitivity to loud sounds

Sensorineural deafness can have a significant impact on your quality of life and well-being. It can affect your communication, social interaction, education, employment, safety, and mental health. However, there are ways to cope with sensorineural deafness and improve your hearing experience. These include:

  • Hearing aids: These are devices that fit in or behind your ear and amplify the sounds around you. They are programmed to suit your level and type of hearing loss and can be adjusted to different situations. Hearing aids can help you hear better and reduce your tinnitus. You can get hearing aids from the NHS or from a private provider.
  • Cochlear implants: These are devices that are surgically implanted in your inner ear and stimulate the auditory nerve directly with electrical signals. They bypass the damaged hair cells and nerve fibres and provide sound information to your brain. Cochlear implants can help you hear better and understand speech more clearly. They are suitable for people with severe to profound sensorineural deafness who do not benefit from hearing aids.
  • Assistive listening devices: These are devices that enhance the sound input from specific sources, such as telephones, TVs, radios, or microphones. They can be used with or without hearing aids or cochlear implants. They include induction loops, infrared systems, FM systems, Bluetooth devices, amplified phones, TV listeners, etc.
  • Communication strategies: These are techniques that help you communicate more effectively with others. They include speaking clearly and slowly; facing the speaker; using lipreading; using gestures; using written notes; choosing quiet and well-lit places; asking for repetition or clarification; etc.
  • Support services: These are services that provide information, advice, guidance, and support for people with sensorineural deafness and their families. They include audiologists, hearing therapists, speech and language therapists, counsellors, social workers, teachers of the deaf, etc.
  • Support groups: These are groups that offer peer support, emotional support, and social activities for people with sensorineural deafness and their families. They include local groups, national groups, online groups, etc.

The audiologist who I saw initially prescribed a pair of Oticon hearing aids, and then upgraded them to Phonak aids, allowing me to keep the Oticons as a spare set.  All my aids are red, my favourite colour, as I am bald and they are always visible.  The NHS doesn’t usually allow adults to choose colours but they made an exception for me when I explained my reasons.  My moulds (the bit that sits inside the ear) are also red.  The champagne-coloured items attached to the bottom of my aids in the picture below are Roger X receivers.  They are paired with a set of portable microphones that I can take to meetings and use to hear speakers more clearly.

A pair of red Phonak hearing aids with Roger X receivers attached.

My aids are programmed to my personal audiogram to allow me to hear as normally as possible. They are also programmed with some optional settings. There is a bass boost feature that is turned on, as well as a speech-in-noise setting that allows me to filter out some background noise and hear speech in front of me. This is most effective when I am actually looking at the person speaking to me. There is also the good old T-coil setting programmed in, which allows the aids to connect to a loop system where available.

Sensorineural deafness is a type of hearing loss that affects the inner ear or the nerve pathways that carry sound signals to the brain. It can have various causes, such as ageing, noise exposure, genetic factors, infections, ototoxic drugs, or other conditions. Sensorineural deafness can affect your quality of life and well-being, but there are ways to cope with it and improve your hearing experience. These include hearing aids, cochlear implants, assistive listening devices, communication strategies, support services, and support groups.

What is Coeliac disease and how does it affect people?

Coeliac disease is a serious condition that affects the digestive system. It is caused by an abnormal immune response to gluten, a protein found in wheat, barley, rye, and some oats. When people with coeliac disease eat gluten, their immune system attacks the lining of their small intestine, causing inflammation and damage. This prevents them from absorbing nutrients properly and can lead to various health problems.

Coeliac disease is not a food allergy or intolerance. It is a lifelong autoimmune disorder that requires strict adherence to a gluten-free diet. There is no cure for coeliac disease, but following a gluten-free diet can help manage the symptoms and prevent complications.

Symptoms of coeliac disease

Coeliac disease can affect people of any age, gender, or ethnicity. However, it is more common in people who have a family history of the condition or other autoimmune diseases. The symptoms of coeliac disease vary from person to person and can range from mild to severe. Some people may not have any symptoms at all, while others may experience:

  • Digestive problems, such as diarrhoea, constipation, bloating, gas, stomach pain, nausea, vomiting, and indigestion
  • Fatigue, weakness, and anaemia (low red blood cell count)
  • Weight loss or poor weight gain
  • Growth problems and delayed puberty in children
  • Skin rashes, such as dermatitis herpetiformis (itchy blisters on the elbows, knees, buttocks, and face)
  • Mouth ulcers and dental enamel defects
  • Bone and joint pain and osteoporosis (weak bones)
  • Neurological problems, such as headaches, numbness, tingling, seizures, and ataxia (loss of balance and coordination)
  • Reproductive problems, such as infertility, miscarriage, and low birth weight
  • Mood changes, such as depression, anxiety, and irritability

Diagnosis of coeliac disease

If you suspect that you or your child may have coeliac disease, you should consult your GP as soon as possible. Do not start a gluten-free diet before getting tested, as this can affect the accuracy of the diagnosis. Your GP will ask you about your symptoms, medical history, and family history. They will also perform a blood test to check for antibodies that are produced by your immune system when you eat gluten. If the blood test is positive or inconclusive, you will be referred to a gastroenterologist (a specialist in digestive disorders) for further tests. The gastroenterologist will perform an endoscopy (a procedure that involves inserting a thin tube with a camera into your mouth and down your throat) to take a biopsy (a small sample of tissue) from your small intestine. The biopsy will be examined under a microscope to look for signs of damage caused by coeliac disease.

In my case, I had a gastroscopy and a colonoscopy on the same day, which took about an hour altogether. The reason for the colonoscopy was that, given the symptoms I had presented with to my GP she was concerned that I might have some form of bowel cancer. Thankfully that turned out not to be the case.

2 week wait referral form for suspected bowel cancer

Treatment of coeliac disease

The only treatment for coeliac disease is a strict gluten-free diet for life. This means avoiding all foods that contain wheat, barley, rye, and sometimes oats. You will also need to check the labels of processed foods for hidden sources of gluten, such as malt extract, modified starch, soy sauce, and some flavourings and thickeners. You may also need to avoid cross-contamination from utensils, cookware, or surfaces that have been in contact with gluten.

Eating gluten-free can help heal the damage to your small intestine and improve your symptoms. However, it can also be challenging and require careful planning and guidance. You may benefit from seeing a dietitian (a specialist in nutrition) who can help you plan a balanced and varied gluten-free diet that meets your nutritional needs. You may also need to take supplements of vitamins and minerals that you may be lacking due to malabsorption.

Living with coeliac disease

Coeliac disease is a lifelong condition that requires constant vigilance and adaptation. It can affect your physical health as well as your emotional and social well-being. You may face challenges such as coping with symptoms, adjusting to dietary changes, managing complications, finding support from others who understand your condition.

However, with proper diagnosis and treatment, you can live a healthy and fulfilling life with coeliac disease. You can find information and support from various sources such as:

Coeliac disease is a serious condition that affects the digestive system. It is caused by an abnormal immune response to gluten, a protein found in wheat, barley, rye, and some oats. The only treatment for coeliac disease is a strict gluten-free diet for life. Eating gluten-free can help heal the damage to your small intestine and improve your symptoms. However, it can also be challenging and require careful planning and guidance. You can find information and support from various sources such as Coeliac UK, NHS, your GP, your gastroenterologist, and your dietitian. By following their advice, you can live a healthy and fulfilling life with coeliac disease.

What is Sleep Apnoea and how does it affect people?

Sleep apnoea is a common sleep disorder that affects millions of people worldwide, and there’s evidence to suggest many more undiagnosed people. It occurs when the muscles in the throat relax and narrow during sleep, causing interruptions in breathing. These interruptions can last from a few seconds to minutes, and can happen hundreds of times a night. People with sleep apnoea may not be aware of their breathing problems, but they often snore loudly and gasp for air. They also tend to wake up feeling tired, groggy, and irritable.

Sleep apnoea can have serious consequences for your health and well-being. It can increase your risk of developing high blood pressure, heart disease, stroke, diabetes, and depression. It can also impair your concentration, memory, and decision-making skills, making you more prone to accidents and errors at work or school. Moreover, it can affect your relationships, mood, and quality of life.

The good news is that sleep apnoea can be diagnosed and treated effectively. The first step is to consult your doctor if you have any of the following symptoms:

  • Loud or frequent snoring
  • Choking or gasping sounds during sleep
  • Pauses in breathing while sleeping
  • Excessive daytime sleepiness or fatigue
  • Morning headaches or dry mouth
  • Difficulty staying awake or alert during the day
  • Trouble concentrating or remembering things
  • Mood swings or irritability
  • Loss of interest in sex

Your doctor may refer you to a sleep specialist who can perform a sleep study to confirm the diagnosis of sleep apnoea. A sleep study involves monitoring your breathing, heart rate, oxygen level, and brain activity while you sleep. You may be asked to wear a device at home or stay overnight at a sleep clinic.

Children can have sleep apnoea too. In fact, sleep apnoea is quite common in children, especially those who have enlarged tonsils or adenoids, which can block the airway during sleep. Other factors that can increase the risk of sleep apnoea in children are obesity, allergies, hay fever, and certain genetic conditions. Sleep apnoea can affect the quality of sleep and the development of children, so it is important to seek medical help if you notice any signs or symptoms of sleep apnoea in your child.

The most common treatment for sleep apnoea is continuous positive airway pressure (CPAP) therapy. This involves wearing a mask over your nose, mouth or both, that delivers pressurized air into your airway, keeping it open and preventing it from collapsing. CPAP therapy can improve your breathing, reduce your snoring, and enhance your sleep quality and daytime alertness.

Other treatments for sleep apnoea may include:

  • Oral appliances: These are devices that fit inside your mouth and help to keep your lower jaw forward and your tongue from blocking your airway.
  • Surgery: This may be an option for some people who have severe or persistent sleep apnoea that does not respond to other treatments. Surgery may involve removing excess tissue from the throat, nose, or mouth, or correcting structural problems that cause obstruction.
  • Lifestyle changes: These can help to prevent or reduce the severity of sleep apnoea. They include losing weight if you are overweight or obese, quitting smoking if you smoke, avoiding alcohol or sedatives before bedtime, sleeping on your side instead of your back, and keeping a regular sleep schedule.

In my case I use an APAP machine (similar to a CPAP but it automatically adjusts the air pressure depending on need) as I also have central apnoeas.  Central apnoeas are pauses in breathing that occur during sleep because the brain does not send the proper signals to the muscles that control breathing. They are different from obstructive apnoeas, which are caused by a blockage in the airway. Central apnoeas can have various causes, such as heart failure, stroke, brain injury, or high altitude. They can also cause symptoms such as snoring, daytime sleepiness, headaches, and mood changes. Central apnoeas can be diagnosed by a sleep study

If you think you or a family member may have sleep apnoea, do not ignore it. Seek medical help as soon as possible and follow the treatment plan recommended by your doctor. By doing so, you can improve your health, well-being, and quality of life.

How to Travel the World with a Wheelchair

Travelling the world is a dream for many people, but it can seem daunting or impossible if you use a wheelchair. However, with some planning, research and creativity, you can overcome the barriers and enjoy the wonders of different cultures, landscapes and experiences. In this blog post, I will share some tips and resources to help you plan your wheelchair accessible trip. I’m Dan McIntyre and I’ve travelled the length and breadth of Europe with my wheelchair, from a gondola in Venice to the Nurburgring in Germany and even stopped by the Police in Monaco.

Choose your destination wisely

Not all destinations are equally wheelchair friendly, so you need to do some research before you book your flight. Some factors to consider are:

  • The accessibility of public transportation, such as buses, trains, taxis and subways.
  • The availability of wheelchair accessible accommodation, such as hotels, hostels, apartments or homestays.
  • The accessibility of attractions, such as museums, monuments, parks, beaches and historical sites.
  • The accessibility of restaurants, cafes, bars and shops.
  • The attitude and awareness of the local people towards disability and accessibility.

You can find useful information about the accessibility of various destinations on websites such as Wheelchair Travel, Simply Emma and World on Wheels. These are wheelchair travel blogs that provide comprehensive reviews and advice on accessible travel for both people with limited mobility and wheelchair users. You can also join online communities and forums where you can ask questions and get recommendations from other wheelchair travellers.

Plan your itinerary carefully

Once you have chosen your destination, you need to plan your itinerary carefully. You want to make sure that you have enough time and energy to enjoy your trip without exhausting yourself or encountering unexpected obstacles. Some tips to plan your itinerary are:

  • Book your flights well in advance and inform the airline about your wheelchair and any special assistance you may need. You can also request a bulkhead seat or an aisle seat for more space and comfort.
  • Book your accommodation in advance and confirm that it is wheelchair accessible. You can also ask for specific details such as the width of the doorways, the height of the bed, the availability of a roll-in shower or a ceiling hoist.
  • Check the opening hours and accessibility of the attractions you want to visit. You can also look for discounts or free admission for disabled visitors and their companions.
  • Plan your transportation options between different locations. You can use public transportation if it is accessible or book a wheelchair accessible taxi or rental car. You can also use apps such as Wheelmap or Access Earth to find accessible places nearby.
  • Pack light and smart. You don’t want to carry too much luggage that can weigh you down or take up space. You also want to pack essential items such as medications, spare parts, tools, chargers, adapters and travel insurance documents.

Be flexible and adventurous

Even with careful planning, you may encounter some challenges or surprises along the way. You may find that some places are not as accessible as they claimed to be or that some services are not available or reliable. You may also face some cultural differences or language barriers that can make communication difficult. However, don’t let these things ruin your trip. Instead, be flexible and adventurous and try to find alternative solutions or opportunities. Some tips to be flexible and adventurous are:

  • Be prepared for the unexpected and have a backup plan in case something goes wrong. You can also have an emergency contact number or a travel agent who can help you in case of trouble.
  • Be open-minded and respectful of the local culture and customs. You may encounter some different views or attitudes towards disability and accessibility that may not match your expectations or preferences. Try to understand their perspective and educate them if necessary.
  • Be friendly and sociable with the local people and other travellers. You may find some helpful allies or new friends who can assist you or enrich your experience. You may also learn some useful tips or insights from them.
  • Be adventurous and try new things that are within your comfort zone and abilities. You may discover some hidden gems or amazing experiences that you would not have otherwise.

Fun facts: The Police stop in Monaco was because I was following the F1 track round at some early hour of the morning and coming off a roundabout the exit I needed was being guarded by a Policeman, so in a slight panic I went completely around the roundabout and started heading back the way I’d come, not noticing the no entry signs. I’d got about 50 yards when I realised it was a one-way street and at the same time I realised that 2 Police cars stuck their lights and sirens on and parked right up to me to ask what I was doing.

The gondola ride in Venice was very expensive but also amazing. There is a jetty with a lift that can take you and your wheelchair down into the boat, so wheelchair users don’t have to leave their chair at all.

Travelling with a wheelchair may seem challenging, but it is not impossible. With some planning, research and creativity, you can explore the world and have a memorable trip. I hope this blog post has inspired you to travel more and make new discoveries, whether that’s abroad or in your own hometown. Happy travels!

A Day on the Waverley: The World’s Last Seagoing Paddle Steamer

Have you ever wondered what it would be like to travel on a steam-powered ship, with the sound of the paddles splashing in the water and the smell of coal and oil in the air? If so, you might want to book a ticket on the Waverley, the world’s last seagoing paddle steamer.

The Waverley is a historic vessel that was built in 1946 and named after Sir Walter Scott’s first novel. She was originally designed to sail from Craigendoran on the Firth of Clyde to Arrochar on Loch Long in Scotland, carrying passengers and cargo. She was operated by the London and North Eastern Railway until 1948, when she became part of the Caledonian Steam Packet Company, a subsidiary of the nationalised British Railways. She wore different funnel colours and logos over the years, reflecting the changes in ownership and branding.

The Waverley continued to serve the Scottish coast until 1973, when she was withdrawn from service due to rising costs and declining demand. She was saved from being scrapped by the Paddle Steamer Preservation Society (PSPS), a charity that was formed in 1959 to preserve and operate historic paddle steamers. The PSPS restored the Waverley to her original 1947 appearance and began to operate her as a tourist attraction, offering passenger excursions around the British coast.

Today, the Waverley is a unique and popular attraction that attracts thousands of visitors every year. She sails from various ports and piers, such as London, Glasgow, Southampton, Bristol, Liverpool, Llandudno and many more. She offers a variety of cruises, ranging from short trips to full-day excursions, along scenic routes that showcase the beauty and history of the British coastline. Some of her destinations include the Isle of Wight, the Jurassic Coast, the Scottish islands, the Thames Estuary and more.

My day on board the Waverley started early one summer morning on the dock in Glasgow, where she sat there resplendent with her red funnels glinting in the sunlight. First order of the day was to get a sausage sandwich and a coffee from the galley. That done we went into the aft lounge to eat breakfast. Then we were off.

What surprised me most about the Waverley was the power produced by the engine and transmitted to the large paddle wheels on either side of her. Within a few minutes we were making good progress to the sea.

Once we reached the sea the Waverley really showed her great strength, increasing her speed and remaining totally stable.

One interesting and quirky feature of the boat is a Royal Mail post box, where postcards can be sent from!

I can’t remember the name of our destination, but it took around 4 hours to get there, and around the same time to get back to Glasgow, but the time flew by for me.

The Waverley is not only a sightseeing vessel, but also a living museum that preserves and showcases the heritage of steam navigation. She is powered by a diagonal triple expansion steam engine that was built by Rankin & Blackmore in Greenock, Scotland. The engine room is open to visitors who can see the engine at work and learn about its history and operation. The Waverley also has a traditional wooden wheelhouse, where visitors can watch the captain steer the ship and chat with him about his experience. The Waverley has several lounges and bars where visitors can relax and enjoy refreshments, as well as a souvenir shop where they can buy exclusive Waverley merchandise.

The Waverley is a remarkable ship that has survived many challenges and changes over her long career. She is a testament to the skill and craftsmanship of her builders and engineers, as well as the dedication and passion of her crew and supporters. She is a national treasure that deserves to be celebrated and supported for generations to come.

If you are interested in sailing on the Waverley, you can check out her timetables, fares and brochures on her official website. You can also book your tickets online or by phone. You can also support the Waverley by becoming a Friend of Waverley, joining the PSPS, donating or volunteering. You can also buy items from her Amazon Wish List or her online shop.

Don’t miss this opportunity to step aboard the world’s last seagoing paddle steamer and experience a day of adventure, nostalgia and fun!