The Henshaw family’s story

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The Henshaw family's story

Patient and Family Stories

Victoria Henshaw was not only a much loved wife, mother and daughter, but an amazing lady who achieved so much in her life both on a personal and professional level.   A town centre manager turned urban academic, Victoria devoted her life to an aspect of cities that is entirely invisible, but which she was convinced had a huge influence over how we perceive places – namely, their smell.  She achieved the successful publication of her book “Urban Smellscapes”, and had begun preparation of a second book which is now being completed by her colleagues.

In 2014, Victoria received the news that she had cancer.  She was cared for by the Hospice at Home team, before being admitted to the Inpatient Unit on 19th September 2014.  Victoria’s family visited daily and were impressed with the peacefulness of the Hospice surroundings, and the privacy and dignity shown to Victoria.

Whilst being cared for in the Hospice, Victoria urged her sons Brodie, Alistair and Oliver to take part in the Colour Assault to give something back to the Hospice.  The boys set up an online fundraising page, setting themselves a fundraising target of £300, and asked family and friends to sponsor them.  Imagine their delight when their fundraising reached over £5,000!

Sadly, only a few weeks after the Colour Assault, Victoria passed away at home.  We are extremely grateful to the family for their support of Rotherham Hospice and we wish them all the very best for the future.

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Shirley and Chas’ story

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Shirley and Chas' story

Patient and Family Stories

Charlie Moody (everyone called him Chas) was told he had cancer on the 22nd October 2001 and very soon a secondary cancer was diagnosed. He was just 42.

Chas was determined he did not want to die in a hospital but his pain and symptoms were such that he needed medical intervention. He came into the Hospice for a week giving Shirley his wife and their 5 children respite whilst Chas had his pain and symptoms managed.

On returning home Chas said to Shirley not to buy him Christmas presents and even said that he would die on Christmas day but he was determined to see the face of his soon-to-be-born grandson. Louis came early and the whole family was able to spend some time together.

Rotherham Hospice provided Chas with specialist equipment and a bed to make his stay at home as comfortable as possible with the help of the Hospice Community Nurses Specialists but by December 24th Chas’ condition had started to deteriorate and he asked to be admitted back into the Hospice.

Throughout that night his condition continued to worsen and Shirley was told to prepare herself. Ashley their 13-year-old son was there to hold his Dad’s hand and Chas died on Christmas morning.

Shirley remembers the Hospice providing such comfort and care and she remembers how Chas knew that the Hospice was where he wanted to die, a place where he could die without pain and be surrounded by the people who loved him.

Since Chas’ death, Shirley and her family have organised a sponsored walk, raising over £400 and Shirley was recently awarded her 5-year service certificate for volunteering in our Maltby High Street Shop and has attended Light up a Life every year since.

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A memory that Shirley shared was about Chas and his Koi Carp. Chas loved his fish and got such a lot from them over the years that when he died Shirley donated them to the Hospice. Koi Carp roam the Hospice fish pond even now.

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Sam’s story

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Sam's story

Patient and Family Stories

In the early hours of Christmas Morning 2018, Sam remembered that she had a couple of presents left to wrap for her and Paul’s two children. At that moment on Christmas morning, she received a call from Rotherham Hospice to tell her that Paul, her partner of 18 years, had sadly passed away at the age of just 45.

This is Sam’s story;

Sam noticed that Paul was beginning to slur his words in the latter months of 2017. The concern for both Sam and Paul was that he had inherited the neurodegenerative disease that had taken the life of his mother and grandfather years earlier. Slurring speech is an early sign of the disease.

Gerstmann–Sträussler–Scheinker syndrome (GSS) is an extremely rare disease that affects only a handful of people World-wide. Paul, having had experience through his family of GSS, went to see a Doctor. Following lots of tests, X-Rays, MRIs, CT Scans, and a trip to Hallamshire in January, the Doctors told him he did not have GSS. In fact, they diagnosed him with Parkinson’s Disease.


By June 2018, and with Paul still riding his bike to work every day, they were both unconvinced with the Doctor’s diagnosis, and Sam began writing down all of Paul’s symptoms and issues, and following tests with a specialist in London in July, Paul was told he had indeed inherited GSS from his mother.

He was told by Doctors at that he had 5 years left, but Sam knew that wasn’t the case. After the huge shock of discovering he had GSS, Paul was referred to Rotherham Hospice.

The week before Christmas, our 24/7 Hospice at Home service came to see Paul. He was agitated and wasn’t responding to communication. Hospice at Home arranged for an ambulance to bring Paul to the hospice. Sam tells us that when he arrived at the Hospice on the Saturday before Christmas, he suddenly seemed comfortable, and much less agitated than in the previous week.

On Christmas Eve, Paul’s family including his children popped to the Hospice to see him, leaving at around 9pm that evening. It was the next morning, on Christmas day, that the phone rang. Sam says she just knew, the moment she heard the phone ring. Paul had passed away.

“I couldn’t ask for any more from the staff at the Hospice. They were all brilliant” Sam says.

The family asked for donations at Paul’s funeral and donated an incredible total of £560 to the Hospice, for which we are extremely grateful. It is donations like that, that allow the Hospice to continue to provide the quality of service that we do to families like Sam & Paul’s.

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Priceless hugs – Dawn’s story

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Priceless hugs - Dawn's story

Patient and Family Stories

“We call them Priceless Hugs” Dawn tells me when she smiles as she explains how much she cherishes visits, chats, and most importantly a hug from our Community Clinical Specialist Nurse Louise.

Dawn was diagnosed with Glioblastoma, the most aggressive form of cancer that starts within the brain, in June this year. This is Dawn & Mike’s story…

“Sparks flew, literally” Mike says, when he recalls how he and Dawn met back in 2000. Mike was a Theatre Nurse, and Dawn was a patient at the time. As fate would have it, the day should have been Mike’s day off, and more than that….. it was Valentine’s Day. Mike sat up with Dawn as she recovered from surgery, and when they briefly brushed hands, they both felt a small electric shock. Sparks flew.

Dawn cheekily smiles when Mike says he spent the next 9 years asking her to marry him. She finally agreed, and the couple were married in November 2009. 10 years ago this year.

Following a previous battle against cancer in the 1990s, In May this year (2019) Dawn started getting painful headaches. The Doctor told her it might just be tension headaches, but that evening Mike found Dawn screaming in agony on the bathroom floor.

“It was like being hit in the head with a baseball bat, over and over again” says Dawn.

The Paramedics were called, and Dawn was taken to hospital. A first CT Scan showed a small bleed. A situation they both thought was curable. But then a Consultant was called and told them both that the small bleed was coming from the tumour…. A tumour neither of them knew existed. Dawn was diagnosed with Glioblastoma.

Louise was the first of the Hospice team to visit Dawn and a friendship was struck immediately. Louise helped to move the couple into priority housing for convenience, she helped sort PIP out, liaised with the Neurology Department at Sheffield Hospital, and referred Dawn to occupational therapy and relaxation classes at the Day Hospice here. 

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Symptom management was also key to the Hospice helping Dawn where we can. But most of all, Dawn cherishes what her and Louise call ‘Priceless Hugs’.

“I’d have Louise here every day. I have to have my priceless hug. I couldn’t have wished for a better person to be here”.

Four months later, in November 2019, and having decided to live life to the fullest, every day, Dawn and Mike renewed their wedding vows on their 10th anniversary. They had a big party afterwards and Dawn was even up dancing! Louise was there and tells us it was an honour to be present. Despite being almost entirely unable to walk, Dawn proudly walked down the aisle.

Dawn tells me that she’s amazed by the generosity of people they’ve met recently. Market traders on Rotherham Market provided flowers and cake for her wedding free of charge. And on a trip to London for Afternoon Tea at Harrods (something Dawn has always wanted to do), Harrods paid for it all, including £500 off a £545 dress that Dawn loves!

Harrods gave her a bouquet of flowers, and they even had their own pianist on the day. Dawn says she burst into tears at their generosity.

The company that Dawn has worked since she was 16 – KP – have been incredible and Dawn and Mike are grateful for how KP have supported them. They still pay her salary, and the couple recently got a lump sum pension which has meant they can do what they want to do.

Dawn’s determination to get things done, and her independence is hugely inspiring, and we wish both Dawn and Mike well as they continue to live their lives to the fullest, raising money along the way, and never forgetting those priceless hugs.

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Our queen mum

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Our queen mum

Patient and Family Stories

Mum was first diagnosed in 2005 with bowel cancer, just one week before my husband died of the same disease. Mum’s cancer returned to her lungs in 2009, when she was 87 years of age. Sadly the prognosis wasn’t good for Mum. However, being the fighter she was, she just wanted to live long enough to celebrate her 90th birthday with all her many friends. So, the battle was on…

Mum returned to her home and received a visit from Margaret Ellis, Day Hospice Sister, who was able to offer Mum a place once a week. Mum was adamant she didn’t want to go, as in her words “You are pegging out when you go there.” I managed to persuade Mum to give it a go, and she absolutely loved it from day one! It gave her a new lease of life. She enjoyed the arts and crafts activities and even painted silk scarves. Mum continued to battle with her illness, visiting the Hospice every week and thriving on it. Finally, in 2011 she got her wish, and we were able to celebrate her 90th birthday with a party for 100 people. We even raised £1000 for the Hospice in lieu of birthday presents!

In February the following year, Mum’s health deteriorated and she was admitted to the Inpatient Unit. Everyone was so committed to helping Mum improve and after a few weeks, she was well enough to go home. Once home, we still had a complete backup from the Hospice at Home Team.

Mum passed away on 30th May 2013.

OUR QUEEN MUM!

Don’t be sad and don’t feel down,
You shouldn’t even raise a frown.
For here’s a lady who led life to the full,
Being in her company was never dull.

That charismatic smile and an encouraging word,
No sounds of negativity were ever heard.
Always in bright colours, her style would never fail,
Even down to the match of her pink finger nails.

Now friends she had many, enough to fill a train,
She loved each one dearly, but none as much as “Our Jane”!
We thought she’d go on forever, but alas it was not to be,
But I’ll bet heavens, now, a brighter, nicer place to be.

We have our happy memories, so there’s no reason to feel glum,
Think of Doreen’s smiling face and say “God Bless to Our Queen Mum!

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Malcolm and Kelly’s story

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Malcolm and Kelly's story

Patient and Family Stories

For Malcolm & Sue and their daughter Kelly May 2018 – one year ago this month – was the month their World was turned upside down. May 2018 was the month Sue was given a terminal diagnosis. Soon after Sue’s diagnosis, the family thought about the Hospice but didn’t know what to expect. It was Sue’s daughter Kelly who strongly advised getting in contact with our team here, having had the experience of the care & support given when her husband’s Nan’s were looked after.

“It’s a place you think you’re going to go into and never come out” Malcolm says. But Sue took the leap and popped into our Day Unit and Malcolm tells us she absolutely loved it.

“Just to see the smile on Sue’s face knowing she was coming to the Day Unit at the Hospice was great”. The Hospice’s pick up and drop off service was a big help to the family, and Kelly tells us it allowed the family to have a break whilst knowing that Sue was being well looked after.

Eventually after a particularly stressful period, and a time that Malcolm says almost broke him, the family got in touch with the Hospice at Home team.

“From the first day the Hospice were brilliant. I found that if I had problems with medicines, the Hospice were always available and always helpful”.

The Hospice at Home team visited up to three times a day and provided necessary resources to ensure Sue’s comfort. Malcolm recounts how surprised and grateful he was that our Hospice at Home team popped round to the family home on New Year’s Day 2019 just to make sure everything was alright, and for a tea and a natter.

“Just knowing someone was coming round and the support we got was always amazing. Right up to the day that Sue passed away, the first place I thought to ring was the Hospice and within an hour, they were here, and had made sure Sue was comfortable.”

Sadly Sue passed away on the 2nd January 2019 surrounded by her loving family.

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Since Sue’s diagnosis, Malcolm has been a wonderful supporter of the Hospice. You may have seen him at The Santa Dash, or at the Tree of Life open afternoon. If not, you will see him at this year’s Glow with the Flow…. He’s even taking on the Sky Dive later in the year.

Kelly still likes to visit the Hospice, visiting the nurses who cared for Sue, and even small things like seeing items in the shop that Sue had bought when she popped into Day Unit, all help Kelly to feel close to her mum.

It is because of our wonderful supporters like Malcolm & Kelly that Rotherham Hospice is able to keep providing the services that we provide.

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My dad, my inspiration

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My dad, my inspiration

Patient and Family Stories

Not all the news from the Rotherham area is bad news! My name is Steven Howard and I have lost both my mum and dad to cancer while they were both fit and had a long life ahead of them, together. I lost my mum to non-hodgkins Lymphoma in 2010 and my dad to stomach cancer in 2016, spending his last days with me at his side in Broom Valley Road Hospice, Rotherham.

Missing them sparked the author in me and I penned my first novel, ‘CURE’, a racy adult adventure thriller based on my feelings and the disease cancer.

Following a motorcycle accident years ago I suffered from PTSD and was forced to give up work as a Yorkshire Ambulance Paramedic in 2008 when, after 18 days of illness that year, I was informed I was no longer capable by management; although I was showing great improvement and had been put forward for promotion to Paramedic Practitioner in Doncaster after the sick days I’d taken. Being forced to find alternative employment found me working away from home, this exacerbated my PTSD but I battled on until the separation anxiety from my family got too much to bear.

That is when I started my own company HART UK Limited and gained contracts with TATA Steel and Scottish Power, where we supplied Doctors Paramedics and Fire Rescue. Selling the successful company in 2011 to spend more time with my daughter and wife made me realise what commitment I had given to Yorkshire Ambulance Service and my company.

Losing both my parents to cancer had focused the realisation of our short time on Earth and so the career in writing began. Writing became a treatment for my PTSD and has benefitted me immensely. As a Yorkshire lad, I am proud that my written work has received such great accolades and would like to think that this county has produced some of the best authors known.

At present, I am using an American Publisher but wish to get my next book, FUEL, published by a UK publisher. I would also love to get my present book CURE published as a UK book! My aspiration is to become a well-known British adult adventure-thriller writer and be added to those great Yorkshire authors.

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As you can see, there is some good comes out of adversity! Thank you for reading my story, I hope that my Mum and Dad are proudly watching over me. God bless you all x.
I cannot speak more highly of the staff at Broom Valley Hospice, where my dad spent his final days.

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Liz’s story

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Liz's story

Patient and Family Stories

My story starts off when in December 2015 I lost my fiancé. He died in Rotherham General Hospital. At the time it was the biggest shock of my life and unexpected. I eventually sought help and wanted counselling, and from a friend, I was referred from my doctors to the Hospice.

I’ve met some lovely people both staff and volunteers many of whom have suffered loss at some time. I go to the group and I have benefited from that too. I’ve met a new friend at the group who is going through the same pain as I am. We help each other. Without all this, I probably wouldn’t be here today. I just put my name down to do voluntary work at the Hospice. I would just like to thank all the staff and volunteers for being so nice and helpful to me.

You’ve helped me realise that life can go on after the death of a loved one and that I am not alone.

If you have been moved by Liz’s story, please consider donating using the button below. Your kind donations allow us to continue providing services and support both in the Hospice and out in the community.

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Josh Oxborough’s story

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Josh Oxborough's story

Patient and Family Stories

“In October, my two beloved granddads very, unfortunately, passed away. Since then, my life has changed massively”.

At just 9 years old, Joshua lost both of his Granddads in the same month after short illnesses brought both Malcolm Oxborough and Brian Gibbins into the care of Rotherham Hospice. Two Granddads who Josh adored and who adored Josh.

Josh tells us that since October last year,

“I’ve had no happy Granddads teasing me and telling me stories about their childhood. No cheerful Granddads sharing their delicious chocolates and biscuits with me.”

This February, Josh decided he wanted to raise money for the two charities that helped his Grandfathers, Cancer Research UK & Rotherham Hospice. He chose the difficult challenge of reading 7 books over 7 days, the ‘Book-a-Day’ Sponsored Read. Books included Dog Zombies Rule by Tom Gates, Farm Boy – The Sequel to War Horse, The Butterfly Lion, and more. Josh produced his own sponsor forms, gained sponsors, and planned the dates for the read; the February half-term school holidays.

Josh successfully completed the challenge, reading all 7 books over 7 days, totalling a massive 21 hours and 1,179 pages! As a result, Josh has raised an incredible £327 for Rotherham Hospice and £327 for Cancer Research, and it is all his doing. Josh tells us that the memory of his Grandfathers lives on.

“I have their voices, cheering me on in my activities, whether it be karate, dancing, or even the Santa Dash that I did in December for Rotherham Hospice. Whether it be at school in my mental maths tests, numeracy ninja tests, or my bulldog games at break. They will always be there with me, squeezing my hand tight, and encouraging me to do more and more.”

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As our Hospice family grows, we welcome key fundraisers like Josh, whose kindness and support allow the Hospice to continue to provide the vital care across all services – from in patient care to Hospice at Home – that helped Josh’s grandfathers.

Thank you Joshua, from all of us here at Rotherham Hospice.

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Jessica’s family’s story

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Jessica's family's story

Patient and Family Stories

The Purple Tulip has become a symbol of remembrance for Jessica and her family. Purple represents the fight against pancreatic cancer, a disease that Jessica’s dad, Keith Horsham, sadly passed away from in April 2019. And Tulip is the name of the room that Keith was in when he spent time at Rotherham Hospice, joking with the cleaning staff, and sitting in his favourite recliner.

This is Jessica’s story:

Jessica’s dad, Keith was a keen golfer. He had been captain of Rotherham Golf Club back in 2017, and it was after returning from a golf trip to Florida in November 2018 that he started feeling a little unwell.

Spurred on by Jessica, Keith reluctantly went to see a doctor having had pains in his feet, and suffering from shortness of breath, which Jessica says was unusual given that he was quite active. The Doctor referred Keith to the hospital, who found blood clots on his lungs.

At first this gave the family some relief, because it could be treated. But soon the hospital found a mass on Keith’s pancreas. The family were told the news they’d feared; the cancer had spread to the lining of Keith’s abdomen.

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Keith was eventually referred to Rotherham Hospice and our 24/7 Hospice at Home team, who stepped in to help with symptom control for Keith at his home. But in mid-March, Keith started feeling worse, and couldn’t eat. Thankfully on the 18th March a bed became available on our in-patient unit here at the Hospice.

The night before Keith came into the Hospice, Jessica says one of the Hospice at Home team sat up all night with Keith, chatting, making sure he was comfortable.
“That was an amazing service to offer.” Jessica tells us.

“It takes a bit of worry off knowing that the nurse knew what to do, and that dad was looked after”.

The next day, Jessica tells us that the family came down with Keith at lunchtime to the Hospice. At first he was nervous, and upset. The feeling of uncertainty was overwhelming, as it often is when people first set foot in the Hospice.

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But before long Keith settled in to Tulip. Jessica tells us the staff couldn’t have been more helpful.

“The nurses are angels.” Jessica says “We are forever in gratitude for their care”.

The time Keith spent in Tulip was comfortable, Jessica explains. They brought in cake for Keith’s grandson’s birthday. His friends popped in to visit, and Keith discovered a new favourite thing…. The ice machine!

Keith Horsham passed away on April 5th 2019 with his children and his family there with him. That day, his friends had came home from a Safari holiday to spend time with him, and his family had had his absolute favourite dinner that evening…. fish and chips.

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Jessica tells us that any time the family see a purple Tulip now, they remember Keith, and the care he received through Rotherham Hospice. Her children can spot a Tulip from anywhere… including a painting on Wickersley underpass. The purple Tulip has become their symbol. Jessica even has a purple Tulip tattoo!

Keith’s family have taken part in several fundraising events for the Hospice including the Colour Run a few years back, as well as Glow with the Flow last year, this year… and Jessica is already signed up for next year! At Keith’s funeral, a collection was taken for the Hospice that raised a staggering £940, and the family intends to hold a big birthday fundraiser on Keith’s 70th birthday.

The support of families like Jessica’s – whether it be through events like Glow with the Flow, or fundraisers put on in the community – is what allows Rotherham Hospice to keep providing the care and support that we provide both in the Hospice itself and out in homes across Rotherham. And for that, we are forever grateful.

Rotherham Hospice relies on the generosity of our supporters. If you would like to leave a donation, please click the donation button below. Thank you.

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