HAPPY BIRTHDAY ROSALIND AMOR!

Happy 30th Birthday to our very own Rosalind Amor and thank you for all your support!

Rosalind’s 10th anniversary of Let’s do it for M.E/30th birthday fundraiser
is on Facebook and JustGiving

Rosalind wrote…

It is difficult to believe it’s now ten years since I private messaged ‘Ricardo’ on Foggy friends, the M.E chat room site, offering to support the newly established ‘Let’s do it for M.E’ campaign. The campaign was aimed at mobilising M.E patients to raise funds for biomedical research into M.E, with the long term objective of establishing a Centre of Excellence for ME in Norwich research park. This Centre of excellence, if it was created, would facilitate clinical examination of patients, translational biomedical research and education for medical professionals. The initial fundraising target was £100,000.

The exotic sounding ‘Ricardo’, who turned out to be our very english teddy Paul ‘bear’ Kayes, invited me to join the Let’s do it for M.E planning group on Facebook. It is extraordinary to reflect on how much I’ve done, experienced and gained since then. I’ve crocheted wristbands, set up a recycle for charity scheme, held a 21st birthday fundraiser, numerous competitions and sponsored events, done a stint as a Let’s do it for M.E blog author, been on television, even met my soul sister!

With the support of Let’s do it for M.E, Invest in M.E Research has gone from strength to strength. We succeeded in raising the initial £100,000. This was used to fund the first PHD student to kickstart the gut microbiota research project. Since then, Invest in M.E has continued to undertake research projects into the gut as well as into B-cells. IiMER now has five PHDs under its belt. The foundations needed for the Centre of Excellence have been laid. Hopefully this will soon become a full reality.

You may be wondering why so much research into the gut? The simple answer is that the gut is the gateway to the immune system. The gut plays a major role in the functioning of the immune system.  This is a fact that has only recently been discovered and even the basics are still yet to be fully understood. One of the reasons the gut plays such an important role in the immune system is because it contains a huge variety of different species of bacteria and viruses. Some of these bacteria are ‘friendly’ bacteria which helps you digest your food. Others are not so friendly. All influence your general health and ability to fight off disease. One of the seemingly common triggers of M.E is an initial infection or virus from which the patient doesn’t recover. It’s possible that changes in the gut microbiota could contribute towards patient’s inability to recover. Such changes to the gut microbiota could also cause local and systemic inflammation. This could explain the inflammation of the brain and spinal cord that has been found in the post-mortems of M.E patients.

Based on their ongoing research into the gut, IiMER are now proposing a clinical study of the effectiveness of feacal (poo) microbiota transplants as a potential treatment for M.E. Feacal microbiota transplants literally involve replacing the existing microbes in your gut with someone else’s friendly ones. This is of particular interest to me. A feacal microbiota transplant has been recommended to me as a therapy by both my specialist consultant and my best M.E friend. My M.E was initially triggered by a virus whose symptoms were very high temperature, nausea and vomiting (including on water). Although it’s never been discovered exactly what virus this was, the symptoms suggest it was a type of viral gastroenteritis (gut virus). Unfortunately I’m not able to take part in the clinical trial as you have to have been diagnosed for less than fifteen years in order to participate and I’ve been diagnosed for 21 years. However I’m hopeful about what the outcome could be. I appreciate that having someone else’s poo syringed down your nose isn’t the most appealing of treatments. However a recent study performed in a single centre in Australia has reported significant clinical improvement in over 70% of it’s M.E patients.

Recently IiMER pledged a further £650,000 towards M.E research which would include the cost to cover this major treatment trial. Some of the money for this pledge will almost certainly need to come from ordinary people crowdfunding. Since Let’s do it for M.E’s inception ten years ago, it’s become a movement with many schemes and people participating. We’re always keen to welcome new supporters however. From raising funds for free whilst shopping online to doing a sponsored marathon and everything in between, there’s something for everyone to get involved with. Check out https://ldifme.org/ for more information.

On a personal note, I’m fortunate to be able to say that my health has improved since my 21st birthday fundraiser. I’m now living in my own home with Madame Pickle (my cat) for company and can eat proper food, rather than being tube-fed. I am able to use a wheelchair, have completed a Open University access module and am just starting a level one module this autumn. Having said all this, my life is still far from being like that of a healthy twenty-nine year old. I hope I will continue to recover but, having already experienced severe relapses, it’s a fear that’s always there.

Because of this, once again I’m asking for donations for my 30th birthday, as I did my 21st. The greatest gift I could ever be given would be to live a healthy life again, unhampered by fear of relapse. IiMER is the best chance I’ve got of receiving such a gift. Plus, it’s also the 10th anniversary of the founding Let’s do it for M.E, which is something that definitely needs celebrating! So please join me in offering a toast, pulling party poppers and, if your finances allow you, giving a donation to continue supporting this vital work.

Let’s do it!

From Rosalind’s 10th anniversary of Let’s do it for M.E/30th birthday fundraiser
on Facebook and JustGiving

Thank you for your support!

The £1 Challenge for Invest in ME Research

We’ve set a new text donations fundraising challenge ending 31st March 2019.

This is the date that all JustTextGiving codes will be deactivated as JustGiving is ending its partnership with Vodafone.

The challenge is for as many people as possible to donate just £1 to Invest in ME Research adding up to a lot of money for the charity’s Biomedical Research Fund to establish medical tests and treatments for Myalgic Encephalomyelitis.

We’re using the JustTextGiving code APFR99 for this challenge.

This text code is linked to our One Day – One Pound JustGiving page.

The text option is UK only but anyone may donate via the JustGiving website from a minimum of £2 (to £100,000!): justgiving.com/fundraising/onedayonepound

The total raised on the JustGiving page is currently over £7,000 (including text donations) so we’ve set an ambitious target of £10,000 to be reached by the time JustGiving deactivates the text codes on 31st March.

Let’s see if we can do it for ME!

Please share widely as every £1 brings us closer to a cure.

If you’re on Facebook we’ve created event pages for 1st February and 1st March but donations are welcome on any day until the end of March for this fundraiser.

 

Best Wishes for 2019 everyone and thank you for your support!

Happy Birthday Paul Kayes!

Let’s celebrate to kick off ME Awareness Month May 2018!

Fab friends of Paul Kayes have been busy organising an online surprise for his birthday today. Paul is co-founder of the Let’s Do It for ME campaign to support the charity Invest in ME Research, and founding admin of The M.E Chat Room Facebook group for Myalgic Encephalomyelitis, among the many ways he shows ceaseless kindness, generosity, and good humour to people across the globe.

Message from Paul’s friends…

Paul as it’s your birthday we all felt that the best way to celebrate was to raise funds for our favourite charity.

Paul you are a great friend you have supported so many of us through good times and bad times and we are honoured to call you a friend so here’s our way of celebrating your special day Happy Birthday 🎁

Many thanks to Nadine Pennington for setting this up and coming up with such a fantastic idea. justgiving.com/fundraising/paulkbirthday

Ways you can help celebrate Paul’s birthday…

🎁 Donate to the fundraising page created by Michelle, Makayla and Sophie: justgiving.com/fundraising/paulkbirthday
(JustGiving accepts any amount from £2 and now has an option to add 5% of your donation to cover their platform fees.)

🎁 Leave a message on the Kudoboard created by Alison: kudoboard.com/boards/j2Tfv2Ks
(It’s easy to register/sign in, click ‘add kudo/image/video’ to type your message, upload image/video or choose from the Kudoboard picture/GIF library.)

🎁 Post a ‘Paul joke’ online to pay him back for all the giggles and groans!

🎁 Join Jen Govey later today in a special birthday surprise for Paul at Dress for ME on Facebook: facebook.com/DressForMEchallenge/

(Update: Jen’s video is here: facebook.com/DressForMEchallenge/videos/1634459776675575/
and she tweeted)…

https://twitter.com/DressFor_ME/status/991429441397149696

Happy Birthday Paul Kayes!

Happy ME Awareness Month everyone!

Thank you for all your support!

£500 matching donations period for Movember 2017!

For this “Movember” for men’s health we have a matching donations period of up to £500! Plus I’ve included a couple of links to some interesting recent research projects which suggest gender differences in ME/CFS.

For those of you who haven’t heard of “Nomenbar for ME” it is LDIFME’s take on “Movember” awareness raising month for men’s health.

It’s true, in common with many other autoimmune diseases, that ME is more common among women than men with an approximate ratio of 4:1.  However men of all ages, races and types still suffer from it.


Do men and women suffer from different phenotypes of the disease? Researchers at the Vall d’Hebron University Hospital in Barcelona recently tried to find out by comparing the characteristics of 1309 consecutive ME/CFS patients (Fukuda-defined). Of the 1309 patients, 119 (9.1%) were men and 1190 (90.9%) were women. The researchers found a number of significant differences between the sexes in a variety of clinical and demographic factors such as but not limited to; age of diagnosis, symptoms and coexisting conditions. It’s still impossible to say from just one such simple study whether this suggests specific phenotypes but, as the authors say, as ME is best seen as a neuro-inflammatory process and there are neuro-immune differences between the sexes it’s quite possible. Read more.

There has also been interesting findings regarding energy metabolism. It’s been proven that all ME sufferers suffer from problems with their Cytric acid cycle; basically the body’s ability to gain energy from carbohydrates. Instead it makes energy from different, lower yielding sources of energy. However it seems there’s a sex difference here too; Øystein Fluge of Haukeland University Hospital in Bergen, Norway, and his colleagues studied amino acids in 200 people with CFS, and 102 people without it. The levels of some amino acids in the blood of women with CFS was abnormally low – specifically for the types of amino acid that can be used by the body as an alternative fuel source.These shortfalls were not seen in men with CFS, but that could be because men tend to extract amino acids for energy from their muscles, instead of their blood. And the team saw higher levels of an amino acid that’s a sign of such a process.” It seems that both male and female CFS patients may have the same obstruction in carbohydrate metabolism to energy, but they may try to compensate differently,” says Fluge. Both sexes had high levels of several enzymes known to suppress pyruvate dehydrogenase (PDH), an enzyme vital for moving carbohydrates and sugars into a cell’s mitochondria – a key step for fully exploiting sugar for energy. Read more.

As usual we are inviting “guest blogs” this month from men with ME telling their story. Email us at fundraising4ME@gmail.com or contact us via Facebook or Twitter if you want to participate

Visit our main Movember blog including links to all the guest blogs since 2015 ldifme.org/2015/11/01/nomenbar-for-m-e/

Visit this year’s JustGiving page solely dedicated to Movember. Remember there is a £500 matching donations period so help us reach our target to raise more for IiMER! Donations can also be made offline but please state when donating offline if it’s specifically for Movember for men’s health  www.justgiving.com/fundraising/nomenbar4me

Thank you for your support!

GIVE IT UPtober 2017

uptober

A simple idea to give up a small luxury during the month of October and donate the saving to Invest in ME Research – a charity run entirely by dedicated volunteers working so hard on behalf of people with ME (Myalgic Encephalomyelitis) and driving progress with a biomedical research strategy to find cause & cure.

We appreciate how few luxuries are left for people with ME, however we are determined and eager to find a cure, and we invite our willing wellie friends and families to join us in giving up a little something in October for ME.

This event has raised nearly £6000 including Gift Aid in the three years it has run, so huge thanks to everyone involved.

Donate on JustGiving at GIVE IT UPtober (worldwide)

Text (UK only) GIUT88 (£1-£5 or £10) to 70070 e.g. GIUT88 £5

Join our group page on Facebook – Give It Uptober

Follow on Twitter #UPtober

Thank you for your support!