We suggest a minimum of £4 per entry but hugely appreciate any amount!
The Pawfect Off is to celebrate Sally Callow's 10 year Anniversary with the famous
ME Foggy Dog - a rather handsome globetrotting adventurer raising funds for CURE M.E!
For this round we have teamed up with Sally and Foggy - learn more about them here
We suggest a minimum of £4 per entry but hugely appreciate any amount!
The Pawfect Off is to celebrate Sally Callow's 10 year Anniversary with the famous
ME Foggy Dog - a rather handsome globetrotting adventurer raising funds for CURE M.E!
For this round we have teamed up with Sally and Foggy - learn more about them here website.
And to learn more about CURE ME who drive biomedical research into ME/CFS please visit their website here.
We welcome and encourage ALL levels and ages of baking & bakers.
This is a fun, light hearted way to raise funds and awareness for a serious cause.
PAWS (pets, animals!) is the theme.
But, any theme, any cake, any bake,
is always welcome!
Your participation is hugely appreciated.
If you have ME/CFS or Long Covid (OR any illness/disability)
We welcome and encourage ALL levels and ages of baking & bakers.
This is a fun, light hearted way to raise funds and awareness for a serious cause.
PAWS (pets, animals!) is the theme.
But, any theme, any cake, any bake,
is always welcome!
Your participation is hugely appreciated.
If you have ME/CFS or Long Covid (OR any illness/disability) which might mean you feel more comfortable to enter with an assigned virtual baking buddy then we can sort this for you.
to find out more.
And/or see COLLABORATIVE BAKER below for more info
In order for us to see your entry we need you to tag us @bake4mecfs or you can attach photo's of your bake on an email.
If we have not reposted or liked your entry after 48 hours then please do drop us an email bake4me.social@gmail.com
to check in.
Go get creative and thank you for supporting.
If you want to enter a bake but you cannot commit because of your illness/disability, we have sourced several COLLABORATIVE BAKERS who would be over-joyed to bake on your behalf!
You still get the fun of participation and creative control...
Our bakers will bake a cake inspired by the idea/concept you suggest.
All you need to do is DM @BAKE4MECFS or email bake4me.social@gmail.com
We know how isolating and limiting it can be to live with chronic illness. And we want as many warriors with ME/CFS, Long Covid, POTS or any chronic illness to feel that they're included.
Meet Jennie Jacques British Actress, avid reader and the creator of BAKE4MECFS.
You might recognise her as Queen Judith,
"I am in my 5th year with an ME/CFS diagnosis; even at the milder end (today) I vouch this is a horrific illness. The science desperately needs funding.
Luckily, I am seeing some improvement(s) to date
Meet Jennie Jacques British Actress, avid reader and the creator of BAKE4MECFS.
You might recognise her as Queen Judith,
"I am in my 5th year with an ME/CFS diagnosis; even at the milder end (today) I vouch this is a horrific illness. The science desperately needs funding.
Luckily, I am seeing some improvement(s) to date which I hope will continue.
But it has been half a decade of living this nightmare and although grateful for the progress/relief to date, in many respects I remain a shadow of my former self.
ME/CFS robs lives - it can be relentless and unforgiving. It
will be my prerogative to fight for the science to be sufficiently funded to help those who do not and cannot recover."
Meet Sally Callow and her Foggy Dog!
And here is Jennie Jacques interviewing Sally Callow! Foggy could not make it
because he was
jet-setting around the USA...
Meet Sally Callow and her Foggy Dog!
And here is Jennie Jacques interviewing Sally Callow! Foggy could not make it
because he was
jet-setting around the USA...
Our long-term goal is to bring about social change for M.E. patients internationally by smashing the stigma with our awareness-raising, changing policy with our campaigning, and funding research that will eventually lead to a treatment or cure."
Sally Callow
Meet
Rosie Brandreth
Honoured to welcome baker and vet, Rosie, back to the judging panel for
the Pawfect Bake Off...
it could not be more pawfect!
Great British Bake Off semi-finalist 2019, Christmas Bake Off Winner 2020! Read more about Rosie here -
Baking From a Vet for You and Your Pet!
"I developed my passion for baking from a young age, g
Meet
Rosie Brandreth
Honoured to welcome baker and vet, Rosie, back to the judging panel for
the Pawfect Bake Off...
it could not be more pawfect!
Great British Bake Off semi-finalist 2019, Christmas Bake Off Winner 2020! Read more about Rosie here -
Baking From a Vet for You and Your Pet!
"I developed my passion for baking from a young age, growing up with my parents and sister in Oxfordshire. We shared the house with various animals throughout my childhood, including a lovely ginger cat I used to chase, and an ever so patient red setter who tolerated constant toy stacking on/around his legs. This led to me training as a veterinary surgeon at Cambridge University, and now working as a vet with horses, dogs and cats. I now have my own menagerie: three dogs (the bulldogs are both hand rears, and as a result, ever so entitled!), two horses, snakes, lizards, a tortoise, chickens and ducks. "
Meet
Felicity Franks
Fabulous and super creative
Pet portrait artist who has supported BAKE4ME in the past and returns as a Judge!
Learn more about her here; website
"My love of art started from a young age, I entered a county primary school collage competition to create the best collage made out of torn up newspaper pages and I won! The pri
Meet
Felicity Franks
Fabulous and super creative
Pet portrait artist who has supported BAKE4ME in the past and returns as a Judge!
Learn more about her here; website
"My love of art started from a young age, I entered a county primary school collage competition to create the best collage made out of torn up newspaper pages and I won! The prize was a life size cutout of Aladdin (I loved it - my Mother did not!), but in that moment I realised I was a creative person and a love of art was born."
ME/CFS is a life-altering and complex multi-system disease that persists for a minimum of 6 months. People who are diagnosed with this chronic illness usually have a very poor quality of life and can often be unable to cope with even general daily activity; taking a shower or brushing teeth can be virtually impossible in some cases.
The illness can fluctuate for a portion of people (moderate to mild) which means they do get some relief on odd days, but even 'mild' ME/CFS is life altering. For others it can be severe and constant.
There are millions of people missing with this illness and sadly many more off the back of LONG COVID. The cause of ME/CFS remains unknown and this is why we desperately need to help the researchers!
We also raise awareness for POTS because there is a strong cross over with this illness and ME/CFS; pregnancy, major surgery, trauma, viral illness sometimes being a trigger. To put it very simply, POTS is a disability which causes an abnormal increase in heart-rate sitting/standing. Many patients need to lay down/rest for long periods of time in a desperate attempt to stabilise.
We have are also adding LYME DISEASE to the list of charity's you can donate to. "ME/CFS has been linked to a number of viral infections, specifically Epstein Barr Virus (EBV) and Human Herpes Viruses (HHV). However, bacterial infections may be another possible source of infection in ME/CFS. Lyme disease is a bacterial infection spread to humans by infected ticks."
Patients can be left bed-bound and house-bound for years due to physical disability and associated chronic pain. There are overlaps with other illnesses such as fibromyalgia, POTS (as mentioned) and even multiple chronic and persistent new infections can sometimes take advantage of the person who is already unwell.
More recently we have welcomed Endometriosis UK to our list. This is the name given to the condition 'where cells similar to the ones in the lining of the womb (uterus) are found elsewhere in the body. Each month these cells react in the same way to those in the womb, building up and then breaking down and bleeding. Unlike the cells in the womb that leave the body as a period, this blood has no way to escape.' Studies have found that over a third of women with CFS report Endometriosis as a comorbid condition.
Imagine lockdown, forever and then inject the flu plus a heavy hangover, with out the partying - you might get an idea of how some days for some people with these sort of illnesses can be. Then add the severe chronic pain which more often than not accompanies the aforementioned. There are no words to describe how bad it can be.
For several decades, those diagnosed have suffered in almost complete silence because the science is criminally under funded. And moreover, until recently, a disgraceful stigma had been attached to those who could not recover from ME/CFS. No one (no one!) chooses to lay in bed for weeks, months or years. Try it for a day or two - or three - keep going if you can - you'll soon discover it ain't no walk in the park; pun literally intended.
Secondary depression and suicidal thoughts or suicide itself are sadly also associated with this horrific illness. We must give people with ME/CFS a voice. And baking contest is just a light hearted way to raise awareness for an illness which is currently robbing more and more lives.
We need your help!
Baking a cake and donating some spare change will contribute to raising awareness for ME/CFS and funds.
ME/CFS can be triggered by many forms of trauma, the most common form is a viral infection. COVID-19 is a potential trigger for many more cases of ME/CFS, which we are starting to see - "post" infectious illness and long term viral damage and debilitation is escalating.
The COVID crisis has presented a unique opportunity to understand how a viral infection — in this case COVID-19 — may develop into ME/CFS in some patients.
#BAKE4MECFS & #CUPCAKES4LONGCOVID is a fun and simple way to show those who are suffering, we hear them and we care!
At Bake4ME/CFS, our mission is to steer the narrative behind this horrific neuro-immuno-metabolic disease in the right direction! We might only be a light-hearted baking contest but we have a lot more cooking in the oven! SHOP HERE for some fun muggaluvvas! And be assured a % of any profit we make will be donated to one of the charities from our list at the end of the tax year.
This Saxon Queen duo from the infamous show Vikings kicked off our first round of baking - actresses Jennie Jacques and Amy Bailey!
For the 2nd Round of BAKE4MECFS we were lucky enough to have English Actress, comedian and writer Miranda Hart join the judging panel! And in collaboration with The Miranda Shop, Miranda Hart is back to judge Round 8! Such Fun!
Talented cake designer and teacher Georgia Green (Georgia's Cakes) kicked off round 3 with the inspirational Anna 'M.E myself and I' who has raised £20,000 since 2013 for ME/CFS!
Round 4 - the spooky special - we were delighted to have Actress and recipe creator Fay Ripley along with GBBO Finalist Helena Garcia on our Halloween bake off judging panel...
Round 5 - The Viking Queen herself helped us to judge the Christmas Round! Do you think she uses her sword to cut the cake?
Round 6 - The Ultimate Story Book Bake Off! We were lucky enough to have Irish Novelist known for works like PS I LOVE YOU! And disabled writer and blogger Lorna @creamcrackeredblog
The STAR bake was entered by Sarah. We read in Sarah's bio that she is an endometriosis warrior! Endometriosis is a long term condition which affects 1 in 10 women. Similar to ME/CFS it is evident that Endometriosis is painfully under researched. We were honoured that Sarah chose to bake to raise awareness for us.
And we very much look for
The STAR bake was entered by Sarah. We read in Sarah's bio that she is an endometriosis warrior! Endometriosis is a long term condition which affects 1 in 10 women. Similar to ME/CFS it is evident that Endometriosis is painfully under researched. We were honoured that Sarah chose to bake to raise awareness for us.
And we very much look forward to sharing Sarah's story behind this 'SUCH FUN' bake.
"My daughters Daisy (age 4) and Bella (age 2) are delighted to have won mini star baker!
We are always keen to support ME/CFS charities as my sister Naomi has suffered from severe ME for over 30 years. She’s incredible, despite all her years of suffering, and she is a wonderful Auntie to the mini star bakers!
Naomi has got a website here,
"My daughters Daisy (age 4) and Bella (age 2) are delighted to have won mini star baker!
We are always keen to support ME/CFS charities as my sister Naomi has suffered from severe ME for over 30 years. She’s incredible, despite all her years of suffering, and she is a wonderful Auntie to the mini star bakers!
Naomi has got a website here, where she shares her writing about life with severe ME.
As well as supporting a good cause that is close to our hearts, the girls and I love baking. Despite their young age, Daisy and Bella have spent many hours baking, and the cake was all their idea. They chose the colours of the cake and loved creating the face on top. They did all the decorating and took great care in making sure the sides were evenly covered with sweets! And of course making sure there were some left to taste along the way!"
"I heard about the competition through Miranda Hart's Instagram page.
I have ME/CFS myself, so I was excited to see a competition to raise awareness and funds. My Mum helped me create this cake over a few weeks of paced baking to make it more manageable for me. I chose to make a sloth, because a lot of the time I feel like due to ME/CFS
"I heard about the competition through Miranda Hart's Instagram page.
I have ME/CFS myself, so I was excited to see a competition to raise awareness and funds. My Mum helped me create this cake over a few weeks of paced baking to make it more manageable for me. I chose to make a sloth, because a lot of the time I feel like due to ME/CFS my body and mind are on a go slow, never getting far despite using all my energy. So I feel quite like a slow sloth! Even though ME/CFS impacts my whole life, I am still me, my own unique individual, with lots to give including a sense of humour and fun. So I wanted to make this cake a bit fun with the happy sloth, and rainbow on the inside, showing that despite ME/CFS I am still here, my own self, and ME/CFS does not define me.
Thanks for running this competition. It means a lot to me to see ME/CFS being recognised, and it is very uplifting to be able to be apart of it! I look forward to creating some more bakes!"