Shop for CF
Take a look at some of the amazing products and initiatives helping to raise vital funds for the Cystic Fibrosis Trust.
The Cystic Fibrosis Trust simply couldn’t do what it does without you. In our fight for a life unlimited by cystic fibrosis we are extremely lucky and grateful to have the support of our amazing volunteers who give up their time and money to support our cause. Many of these wonderful people have kindly developed some exciting supporter initiatives to help raise additional funds in aid of the Trust. Take a look at the array of items below and see if anything takes your fancy!
If you have a fundraising initiative that you would like us to promote, your Community Fundraiser would love to hear from you.
Thank you so much for all your support!
Exercise.co.uk
Roger Black Fitness has partnered with Exercise.co.uk and Cystic Fibrosis Trust so that every time they sell any products in the Roger Black Fitness range, they donate £5 to the Trust.
Exercise.co.uk is an online retailer based in East Yorkshire selling fitness equipment to customers throughout the UK.
"When picking our charity of the year personal ties within the business guided us towards choosing the CF Trust, but we are also aware of how important exercise is to those suffering with CF. Following the pandemic, we wanted to make exercise accessible to as much of the UK as possible whilst donating to charity at the same time, allowing us to raise awareness and money for a cause close to our hearts.
Check out the Roger Black Fitness Range and for every purchase we’ll donate £5 to the Cystic Fibrosis Trust!"
Roger Black Fitness Range
Holy Cow Clothing Ltd
Holy Cow Clothing Ltd is an online design & fashion store founded by Sue (Mum) & Nat (Daughter), based in Sheffield. Unique, on-trend designs brings you unisex fashion with a social conscience.
“We have a BIG mission to fulfil! To design exclusive clothing collections for charities close to our heart with the aim to raise funds & social awareness. Our very first 27 piece collection has been designed for the Cystic Fibrosis Trust for Adults & Children. Inspired by my Daughter’s 5 year old school buddy, Henry- he is our very own local CF superhero.” - Nat
“Our 3 exclusive designs are ‘Just Breathe - Dragon’, ‘Just Breathe - Slogan’ in yellow & black text.
And the 3rd design is our ‘65 Roses’- inspired by the beautiful story of a child trying to pronounce the disease ‘Cystic Fibrosis’. My creation was to strategically place 65 individual roses in the shape of a heart to show the love we have for the CF community. The roses are the colour yellow to represent the CF Trust’s main colour.” - Sue
It’s an absolute pleasure to support such a wonderful community and we hope you enjoy our unique fashion. We donate a HUGE 20% of the ‘Retail Price’ per Charity Style order to the ‘CF Trust’.
Full Collection available here https://www.holycow-clothing.com/collections/cystic-fibrosis
Please follow our Instagram page - @holycow_clothing
Please follow our Facebook page - https://www.facebook.com/holycowclothinguk
Please follow us on Pinterest - @holycclothing
Blue Star Adventure
Back in 2015, Staffordshire yachtsman Mike Goodwin sailed around Britain with his friend Roger Colmer in their yacht Blue Star, raising a whopping £30,000 for the Cystic Fibrosis Trust along the way!
Mike and Roger have now come together again to write a book that tells of all the amazing challenges they experienced during their incredible voyage.
All author royalties will be generously donated to the Cystic Fibrosis Trust, in memory of Mike’s son Dan. The book, ‘Blue Star Adventure’, is available in bookstores nationwide, but Mike is keen for would-be readers to buy the book from him personally as this will enable him to donate the bookstore margin, and thus make a bigger overall donation to charity.
Anyone who would like to buy a copy of the book from Mike may contact him via email. The book is priced at £14.99 paperback and £19.99 hard back.
Fi’s Amazing Brownies
Fi’s Amazing brownies, based in a small village in Wiltshire, sells made to order Belgian chocolate brownies that can be hand delivered locally or posted all over the UK. The brownies contain honeycomb, fudge, marshmallows, chocolate chunks and more, so every bite is different! 20% of the profits each month go to the Cystic Fibrosis Trust to support Fi's amazing great nephew and others living with cystic fibrosis.
You can find Fi's brownies at fisamazingbrownies.co.uk or on Instagram @fisamazingbrownies and Facebook @fionasamazingbrownies.
Nalu Beads
A big thank you to Nalu Beads, who have created a beautiful edition to their charity range in support the of the Cystic Fibrosis Trust.
From Nalu: "This year we worked closely with Daniel Longhurst to design this beautiful bead. Dan has been a long time supporter of Nalu Beads and is affected by CF, thanks to him we can finally show our support to everyone who is affected by this condition"
£2 from each sale will come to the Cystic Fibrosis Trust, which can be purchased here, as well as other wonderful gifts ideal for Christmas. Thank you Dan and Nalu Beads for your wonderful support!
Breathe With Me
Breathe With Me is a release by emerging Indie pop artist Betsa, that aims to focus public attention on cystic fibrosis (CF) and the campaign for access to new precision medicines on the NHS.
Well-known music producer Simon Ellis (who has worked with artists like S Club 7, Britney Spears, The Spice Girls) produced Breathe With Me. He had also previously worked with Betsa and when he approached her to perform on the track she was delighted to volunteer her services for such a good cause.
The resultant song is an upbeat number, with a video that features people who are living with cystic fibrosis including Veronica Lanzetta, who had a double lung transplant in 2015.
“The song is about understanding and relating to what others might be going through. In this video I had diseased lungs painted on my back” said Veronica. “The front of me was painted with beautiful roses, to signify new life and hope after my transplant, and also because ’65 roses’ is a symbol that is used often in the CF world. Young children find it difficult to pronounce cystic fibrosis – one little boy called it 65 roses and the phrase stuck.”
“We hope that the cystic fibrosis community will find many innovative ways to let people view the YouTube video for ‘Breathe With Me’ – They can share it on social media, play it at events and if anyone has contacts with local radio – perhaps they can also ask for it to be played on their local station.”
Elizabeth Sheahan (15) also took part in the video because she is putting her all into advocating for access to cystic fibrosis precision medicine. Her scenes were filmed underwater – an apt location to remind people of the panicky feeling of being unable to breathe as normal.
Eight-year-old Emma Frank was filmed blowing bubbles (a visual way to show breath). Some of the bubbles that she blows in the video have the ‘No More CF Angels’ rose image in them - an image used often in the campaign for access to CF precision medicine.
Seasoned CF campaigner little Ivy Weir (5) also has a cameo role in the video.
The Breathe With Me video can be viewed on YouTube, downloaded from iTunes in aid of the Cystic Fibrosis Trust, purchsed from CD Baby or Amazon, or streamed on Spotify.
Follow for more about ‘Breathe With Me’ and CF on the Strawfie Challenge facbeook page or on the Breathe With Me website.
Kirsty Harvey - An Inspirational Life
This beautiful portrait was painted by Kirstin Heger following the passing of her good friend Kirsty Harvey, who lost her battle with cystic fibrosis on 26th May 2018 and is fondly missed by her husband Dougie Harvey and her loving family and friends.
Kirstin was inspired to paint this portrait which was based on a photograph posted by Kirsty in the weeks before she passed away, and in true Kirsty style it showed her beautiful, eccentric, colourful, whacky, fashionable and stylish side.
"You would never have known someone was as ill as she was as she smiled widely at the camera and looked as fabulous as ever! She was without a doubt the most positive and inspirational person I have known and touched so many people in this way. Kirsty loved anything unicorn related and the symbolism of the mythological creature is not lost on her, she was a truly magical being"
Kirstin is selling prints, with all profits being donated equally to the Cystic Fibrosis Trust and Live Life Give Life charities.
Order a copy here.
Andrew Alan Matthews art
Artist Andrew Alan Matthews is raising funds for the Cystic Fibrosis Trust in support of his close family members who have the condition. He has produced a range of modern cityscape paintings on canvas and a range of t-shirts. For each t-shirt sold, £1 comes to Trust, and with every canvas painting sold £5 is donated to the Trust.
Paintings can be commissioned, and prices start from £100 where a proportion would go to Cystic Fibrosis Trust.
Andrew has sold artwork to companies and private collectors and is a bestselling artist on the online platform Artgallery.
If you would love one of these modern cityscape paintings or any t-shirts please go to andrewalanmatthews.co.uk where you can see further examples of his fabulous work.
See Your City
See Your City is a tour operator based in London, Edinburgh and York. The company has a fine selection of cultural tours, both pop and historical. Walking tours are suitable for all ages and will have you marvel at the cities you thought you knew. We are proud to say that 10% of See Your City's profits will come to the Cystic Fibrosis Trust, as their charity of the year.
To find out more, visit their website.
McAdam Art
Our amazing supporter Sheila McAdam lovingly paints and designs bespoke watercolours of flowers and certain wildlife. Each individual piece is made in support of Sheila’s beautiful great niece Freya who has cystic fibrosis, with all profits kindly donated to the Cystic Fibrosis Trust.
Paintings can be commissioned of any flower and prices start at £100, with postage and packaging as extra.
All paintings are sent mounted with a backing board and cover sleeve. They measure approx. 20in x 16in
If you would love one of these beautiful and individual pieces contact McAdam Art or visit Sheila's Facebook page, where you can see further examples of her work.
ALL proceeds from the sale of this book will go to the Cystic Fibrosis Trust.
Head over to Ebay to purchase the book - you will receive a PDF (45MB) file.
Charity Car
Charity Car is a scheme backed by CarTakeBack, the UK's largest car recycling network. Head to the Charity Car website, and select the Cystic Fibrosis Trust as your chosen charity - the Trust will receive 100% of the car's scrap value, and if there's enough life left in your car, Charity Car will raise the maximum value through auction!
Do something really special and join the thousands of people who have already donated their car.
Reusable cotton tote bags
We are so excited to share, on behalf of the South Lincs branch of the Cystic Fibrosis Trust, this fantastic reusable cotton tote bag. 100% of the proceeds will be donated to the Trust to help us continue our fight for a life unlimited by cystic fibrosis.
The duck is a symbol of remembrance for a very dear lady lost to cystic fibrosis. Helen Bond was a founding member of the South Lincs branch of the Cystic Fibrosis Trust. She was an avid collector of rubber ducks with over 100 different pieces in her collection! She lost her battle with cystic fibrosis in December 2014, aged just 28 years. The continued use of the rubber duck keeps her memory alive to all those who knew her, and helps the South Lincs branch spread awareness of the condition.
If you would like to get your hands on one of these limited edition bags (currently only 1,000 in circulation), please get in touch with the South Lincs branch directly by private messaging their South Lincs Facebook page.
Bags cost just £3 each plus postage and packaging.
Cupcake toppers
The lovely team at My Cupcake Toppers have kindly agreed a reduced rate for our supporters to purchase either rice paper or edible icing cupcake toppers! They start from £1 (+ postage and packaging) and are available in two designs - 'Cystic Fibrosis Trust' logo, or 'Cystic Fibrosis why we're baking'. Head over to My Cupcake Toppers to order yours now, or call them on 0800 043 4557 or drop them an email.
Duck pin badges
We're happy to share these gorgeous duck pin badges on behalf of the South Lincs branch of the Cystic Fibrosis Trust. 100% of the proceeds will support our fight for a life unlimited by cystic fibrosis. The duck is a symbol of remembrance for a very special lady lost to cystic fibrosis, Helen Bond. Helen was a founding member of the South Lincs branch - and an avid collector of rubber ducks! She lost her battle in December 2014 aged just 28 years old. The rubber duck keeps her memory alive and helps the branch spread awareness of the condition. To get hold of your very own duck pin badge, send a private message to the South Lincs branch Facebook page.
Etsy knitted toys
Lesley & Julie from Rugby have set up their own shop on Etsy, selling their handmade knitted toys with 100% of the sale price coming to the Cystic Fibrosis Trust. To order yours today just head to their page on Etsy.
Wristbands for cystic fibrosis
A new style of wristband has been designed and produced to raise funds for the Cystic Fibrosis Trust.
The Apter family along with a group of friends have produced the wristband to raise funds for the Trust in memory of their lovely son James. James had cystic fibrosis and was also diagnosed with leukemia in April 2011. He lost his battle against leukemia on 8 September 2011. Selling the wristbands will keep James' memory alive whilst raising funds for a charity that is very close to his family's hearts. Order your wristband today.
These Are Our Days
A song performed by St Aidan's CE High School, Harrogate to raise funds to support the Cystic Fibrosis Trust, in memory of former St Aidan's student Helen Hawcroft. Download from iTunes. All proceeds will be donated to the Trust..
The Little Cook Book
'The Little Cook Book' written by Alex Sayers for her son Enzo has already raised over £13,000 for the Trust. The cook book was inspired by meals savoured during a childhood spent in Italy watching her Italian grandmother in the kitchen.
The easy to follow recipes include 'Nonna Lisa's Meat Balls', 'Italian Chicken', 'Creamy Mushroom Pasta', 'Sausage Bake' and many more tempting recipes.
TV Chef Gino D'Acampo has also contributed two recipes as well as personal trainer Ben Mudge.
The cook book is still available at £10 with all proceeds going directly to the Trust.
Please contact Alex Sayers via email at [email protected].
Portraits of cystic fibrosis book
Photographer Simon Wiffen's book '47 / A Life With Cystic Fibrosis' is a collection of intimate and compelling portraits, exploring the realities of living with cystic fibrosis.
Each subject featured in the book offers their insight into life and the condition.
For each copy sold, £5 will be donated to the Cystic Fibrosis Trust. The book is available to order from Simon's website for £20.
PopFlo Childrenswear
PopFlo Childrenswear is a family owned and operated business with beautifully chic and playful clothing for ages 0-24months. Owner Rosie was inspired by her daughter Poppy and Poppy’s brave fight with cystic fibrosis.
PopFlo have generously donated 10% of all their profits go to the Cystic Fibrosis Trust. For the cutest styles in every season, you simply must check out PopFlo Childrenswear!
Instagram: @popflochildrenswear
Website: www.popflochildrenswear.co.uk
Kayleigh Makes Studio
Discover the colourful, happy, and whimsical world of Kayleigh Makes Studio, where each piece of handmade polymer clay jewellery brings joy and spreads awareness. Shop online through Etsy and support Kayleigh, who battles cystic fibrosis, as 10% of every purchase goes towards the Cystic Fibrosis Trust. Join us in spreading happiness and making a difference with every unique creation.
KayleighMakesStudio - Etsy UK
Lyndsay Mhairi Photography
I am Lyndsay and I set up Lyndsay Mhairi Photography after finishing studying photography at college in 2016.
I photograph mainly landscapes and sell them at local craft markets. I have sold on Etsy during 2020/2021 and have recently launched my website this year.
https://lyndsaymhairiphotography.com/
10% of profits from all products goes to Cystic fibrosis trust at the end of the year!
I started this due to me being on the lung transplant lift and due to that I couldn't get a job, I started selling my photographs at markets as I could take photos on good days and edit my work on days i was struggling more. My mum would come and help out at the markets with me as I would get tired.
I am still selling at markets but I am now off the lung transplant list due to kaftrio being made available.
I love getting out into nature and photographing the stunning Scottish landscapes.
I have sold work to America in the past. at the moment my website is for UK only but hope to open it up in the future to other countries