Showing posts with label centre of excellence. Show all posts
Showing posts with label centre of excellence. Show all posts

1 September 2015

1st of the month - the day to donate £1 to 1st Class ME Research!

A Pound For Research

The original idea by Ruth Gilchrist for One Day - One Pound was for as many people as possible to donate just £1 on May 12th International ME Awareness Day to show support and to help raise vital funds for 1st class biomedical research for tests and treatments for ME (myalgic encephalomyelitis).  We extended this to include a monthly reminder of our ongoing fundraising for this vital cause on the 1st of each month.  Donations at any time are welcome. Every £1 makes a big difference to the charity that our cause supports - Invest in ME (also now registered as Invest in ME Research). 

Gift Aid is an extra 25% of your donation from the government if you are a UK tax-payer,
so don't forget to tick the Gift Aid box when you donate if this applies to you.

If in UK you can text APFR99 

£1-£5 or £10

to 70070 

(JustTextGiving)

Text donations add to the total raised on the Just Giving Page.

You can add your name and Gift Aid if eligible by text. 

You can also donate (worldwide) 
any amount (minimum of £2) via JustGiving

Other options to donate £1 or more .. 

Paypal

To: paypal@investinme.org

Bank Transfer

Bank: Lloyds TSB Eastleigh

Sorting code: 30-92-94

Account number: 02252685

Bank Transfer from outside the UK 

IBAN: GB63 Loyd 3092 9402 2526 85

BIC/SWIFT: LOYDGB21209

Cheque

Send cheques payable to ‘Invest in ME’ to:
Invest in ME 
PO Box 561,
Eastleigh,
Hampshire,
SO50 0GQ
(add Gift Aid to your donation with Invest in ME’s Gift Aid form)

Please help spread the word .. 

Let's Do it For ME is a patient-driven campaign launched in 2011 in support of the proposal by independent UK charity Invest in ME (Research) to establish a centre of excellence for translational research and patient care based around Norwich Research Park in East Anglia; the first of its kind in UK/Europe and in collaboration with other leading UK and international biomedical researchers.

We help to raise funds for the biomedical research into myalgic encephalomyelitis that the charity is organising and/or funding in the development of the centre of excellence projects. The foundation study investigating the role of gut permeability in ME got underway in 2013 thanks to achieving our initial fundraising target of £100k (new target £200k) The next £50k fully funded a study of B-cells based at UCL prior to a clinical trial (new target £450k)

Our crowdfunding for specific ME research is the first of its kind in UK and has inspired similar projects in Europe and USA. We have now helped to raise over £500,000 for the IIME Research strategy to develop and are aiming for £1000,000. The current focus of the research is on the role of the immune system, including infection and autoimmunity. 

Invest in ME is run entirely by unpaid volunteers who either have ME or are parents and carers of ME patients. They are driving the agenda of scientific biomedical research into diagnostic tests and treatments for myalgic encephalomyelitis in UK in collaboration with international researchers of world renown. Thank you for your support! 


Let's Do It for ME!
in support of Invest in ME (Research)
Invest in ME International Conference (IIMEC)
IIME/UCL/UK rituximab trial 

You can follow our cause @Letsdoit4ME on Twitter and find us on Facebook


Thank-you for your support!

1 February 2015

Great Start to 2015!

Wow, thanks to everyone supporting, what a busy start to the new year, hard to believe that January's over so soon! This is a landmark year, as 2015 marks the 10th year of Invest in ME charity and the 10th of their renowned international biomedical research conferences (IIMEC10). You can read more in the first Invest in ME newsletter of 2015, published in pdf on 27th January - http://bit.ly/1wAnt7L  You can sign up to receive their free e-newsletters by email
Jam-packed as usual with news of their amazing work on campaigning, advocacy, education, and with updates on the research and fundraising on pages 8 and 9 of the pdf. You'll see links to some of the new fundraising events organised so far for 2015 including: Walk for ME, Twighlight Colourthon, Brighton Half-Marathon, Sheffield Half-Marathon, Brighton Half-Marathon, Thames Path Challenge, Tough Mudder South-West, 2015 miles of running in 2015, A Birthday Challenge. 

Also new for 2015 is the New Year, New ME fundraiser, an all-year round extension to the very successful Stoptober for M.E. Awareness and fundraiser organised by Ali Head, whereby supporters gave up something they enjoy and donated what they saved to Invest in ME. Aimed at the family and friends of people suffering with ME in hope that they will support the search for treatment and an end to the neglect of this devastating disease. Event info here -
https://www.facebook.com/events/852973618102072

Watch this space for the launch of The Big Sleep for ME 2015. Meanwhile, Team Princess is polishing up their tiaras in readiness to play their role. You can find them on Facebook here - https://www.facebook.com/meprincesses 

Two more major awareness and fundraising events are Mike Harley's EU Marathons and Mike Shepherd's North Pole Challenge. You may remember Mike Harley from last year as Team Leader of 92 for ME, the amazing tour of 92 football league grounds in 92 hours. He's now embarking on a mammoth challenge to run a marathon in 28 EU countries! Mike's EU Marathons Facebook page is here - https://www.facebook.com/mikeseumarathons

Mike Shepherd's North Pole Challenge is set for April 2015 and is all the more remarkable as he will be the first person with a heart pacemaker fitted to run a full marathon at The North Pole. Mike's wife Lara has fibromyalgia, and he is doing this amazing challenge for the sake of his teenage daughter Elizabeth, as she has had ME for several years of her young life. Mike's North Pole Challenge Facebook page is here - https://www.facebook.com/Northpolechallenge

Sue Page's Small Change to Change M.E. Fundraiser will run again throughout 2015. The £2014 target was reached by 31st December 2014, so Sue has raised the target for this year to £3000. Loose change – it all adds up! The event page is here - https://www.facebook.com/events/1536858226585701/

You're welcome to let us know if you're planning any events for Invest in ME, or if you'd like to help out in any way with our awareness and fundraising in support of the charity.  We are mostly severely ill and the charity itself is also run by volunteer patients or parents/carers, with no paid staff.

Current Invest in ME Research Fund Totals are:

Gut Microbiota Research - £130k raised of £200k target.
Rituximab Research - £368k of £450k target. 

So, just £2k shy of a whopping £500,000 raised for Invest in ME Biomedical ME Research Funds since our campaign launched in July 2011 support of the charity's proposal (published May 2010) for a centre of excellence for translational biomedical ME research and patient care! 

Oh, is 1st of the month? The day to donate just £1 to IIME's 1st class biomedical ME research!


Thank-you for your support.
 
Let's Do It for ME
in support of Invest in ME (Research)
Invest in ME International Biomedical Research Conference (IIMEC)
IIME/UCL/UK rituximab trial 
 
  Let's Do It for ME is a patient-driven campaign helping to raise awareness of the work of independent UK charity Invest in ME (Research) on developing a UK centre of excellence for M.E. and funds for the biomedical research into myalgic encephalomyelitis that the charity is organising and/or funding. Invest in ME is run entirely by unpaid volunteers who either have ME or are parents and carers of ME patients. They are driving the agenda of scientific biomedical research into diagnostic tests and treatments for myalgic encephomyelitis in UK in collaboration with international researchers of world renown. 2015 marks the 10th year of amazing progress made by this small charity with a BIG cause. Will you help them make it the best yet? Let's do it for Invest in ME!

29 September 2014

Welcome to IIME September Newsletter!

We said in our 1st September update that August had been a busy for month for Invest in ME Charity  
and their supporters. Well, this month has followed suit! 



Invest in ME Research Charity
This rapid progress is enabled *THANKS to YOU ALL* for your tremendous support and generous donations to Invest in ME. IIME writes:
"There are real grounds for optimism now that the charity and its supporters have been able to build a foundation for a long term strategy of biomedical research into ME."
The jam-packed pdf version of the Invest in ME September 2014 Newsletter is a round-up of the two e-newsletters published by the charity this month.

This new pdf format is a taster of things to come, as they intend in future to produce a fuller magazine to accompany the newsletter. This will transform into a monthly document which describes the work that the charity and their supporters are doing together.

 
From the Introduction:

September 2014 IIME Newsletter
Our foundation project has begun at University of East Anglia and the Institute of Food Research to analyse gut microbiota in ME patients.

At the 2012 conference we stated that we were working on an attempt to set up a rituximab clinical trial. Following our Biomedical Research into ME Colloquium in London last year we have made rapid progress by partnering UCL in setting up the planned UK rituximab clinical trial.

In our ninth year as an organisation we can say each year has been a stepping stone in breaking the mould and bringing ME into mainstream in research and media.

Funding is scarce and the efforts of our supporters to make up what has been lacking from government agencies and research funding organisations have been awe-inspiring.


Please have a read and let us know what you think of the new format! 

You can also -

Click here for the web version of the 1st September 2014 IIME Newsletter.


Click here for the web version of the 22nd September 2014 IIME Newsletter.


Coming up in October ...
  • 1st of the month - the day to donate just £1 to Ist Class Biomedical ME Research!
  • Stoptober Stop for M.E!
  • Scary Bear Halloween Event! 
Invest in ME Research Charity

Thank you for you support!

Let's do it for ME!
created in support of 
Invest in ME Charity

18 September 2014

Hurst Family Fundraising for ME!

Jane Hurst
I have suffered with this horrible illness – ME – for over 16 years. I also have Dysautonomia, and was recently diagnosed with Elhers Danlos Syndrome. I have too many symptoms to list, most of them invisible, but the symptoms that cause me most distress are the severe chronic pain and the disabling and very uncomfortable circulatory/cardio vascular problems. I spent the first 2-3 years of the illness completely bed-ridden & all of the past 16 years housebound (mostly bed-ridden) but due to the pain I experience now I am unable to lie down and sitting down is too painful a lot of the time, so life is extremely difficult, having to stand hunched over my bed for hours each day even though this causes me to feel very faint & exhausted. I try to be positive but if I’m honest most days are nothing short of an endurance. This is also the case for many of my fellow Severe ME/EDS sufferers.

2013 Picture Quiz
Back in 2000 I felt I just had to do something to help raise both awareness of this illness and funds for ME research. I decided I would organise a trivia quiz. It took months to compile but eventually it was complete and, thankfully, it raised over £400 for ME Research. I went on to do another 7 more quizzes and 2 years ago Geoff came on board and our 2 quizzes have raised a total of £2100 for Invest In ME. Lets Do It For ME helped us to reach this total as did our families, and of course our friends who were so generous with donations. We hope to organise another quiz later this year. Geoff’s a great quiz partner (don’t tell him I said that though!)

Profits to Invest in ME and The 25% M.E. Group
Back in 2004 I put together some Nature photocards to raise money for various ME Charities. All photos I use for the the cards are taken by either people with ME or the families of PWME. We got 20 packs of each design printed up and thankfully they sold! And incredibly they still do sell! Profits from the photocards go to Invest In ME and The 25% M.E. Group. Alongside the photocards I’ve been making my own greeting cards since 2005. Due to the illness I can usually manage two 20 minute card-making sessions a day and even during these better hours it’s often frustratingly difficult to concentrate due to the pain and vertigo I experience, this is one of the reasons I keep my designs pretty simple, plus I’m not talented enough to create anything too complex! 

Range of Designs
Supermarket Display


My family have been brilliant and organise sales three times a year at our local supermarkets and our local Farm Shop sell my Easter and Christmas cards. We all just want to do our bit to help raise awareness and funds for this horrible horrible illness that unfortunately can and does destroy lives. Over the past 13 years the cards and the quizzes have raised over £11,000 (£2000 of this was raised by the online quizzes Geoff Allen and I organised). Hopefully the cards will continue selling and hopefully Geoff and I can think of some more quiz questions so we can launch a 2014 Trivia/Picture Quiz later this year! Thanks for reading :-) Jane Hurst.


Hurst Family Sales of Jane's Cards
A big THANK YOU to Jane Hurst and family for their tremendous efforts and achievements in raising awareness and vital funds for biomedical research into myalgic encephalomyelitis, and not forgetting quiz-partner and fellow Let's do it for ME Team member Geoff Allen. Together, they embody the true spirit of our can-do community campaign 
in support of the progressive work of 
Invest in ME Research charity in developing a UK centre of excellence for ME.  

Jane has two sets of photocards now with new designs. Click below for details.

Pack 1         Pack 2 

Cards for all seasons to Invest in ME all year round!




27 July 2014

Good Things Come in 3s - We're 3 Today!

Good things come in threes! It's been three years since three house/bed-bound ME sufferers launched Let's do it for ME to highlight and support the work of Invest in ME, crowdfund vital research into the disease and help the charity progress its plans to establish the first centre of excellence for ME in the UK.

Lots of good things have happened in the last three years thanks to your support. If you have ever donated, shared or helped us in any way, please take this time to congratulate yourself for the part you have played in the following achievements:

  • Building of team work and a great community spirit, not least our planning group as people, inspired by the aims of the cause, got together to make it a success.

  • Increased awareness through all sorts of creative fundraising events, poems, books, music, crafts and audio plays - ldifme.org, facebook.com/ldifme

  • New researchers bringing their expertise to the field of ME research, including Professor Simon Carding, leader of the Gut Health and Food Safety Programme at the Institute of Food Research, UEA, and Professor Jonathan Edwards, Emeritus Professor of Connective Tissue Medicine, UCL, who pioneered the use of B cell depletion therapy (rituximab) to treat rheumatoid arthritis.

  • Funding of the foundation gut research project and a PhD studentship at UEA as well as the initiation of this work - recently featured in the Institute for Food Research Newsletter.

  • Funding and initiation of preliminary B-cell study for a UK rituximab clinical trial at University College London.

  • The three most successful IiME international biomedical research conferences and pre-conference research meetings yet, fuelling collaboration between researchers and educating health professionals. This year, as well as a CPD accredited conference DVD (not yet released), IiME have produced a Booklet to educate GPs and other healthcare professionals about the current state of research into ME that includes a summary of the research meeting and conference by Professor Jonathan Edwards.


Also in progress:

  • The initial target for the UCL/IiME rituximab clinical trial is 98.9% funded, so close! - ukrituximabtrial.org


  • Invest in ME and Let's do it for ME are also working toward further research projects that will complement the existing ones, and our initial plan of a centre of excellence is still the main target of our work.



Our ability to initiate research projects and progress plans for a centre of excellence is due in no small part to the many people who have taken the time and effort to get involved so thank you..  and Happy Birthday!
from all at LDIFME and IiME

1 May 2014

ME Awareness May 2014!

Quick one-stop shop post for links to the various events organised by Invest in ME or their supporters - spoilt for choice with something to suit all ages, tastes and abilities, so we hope you will join in and please let us know if there are any missing links or if you'd like a link added as we'll try to keep the post updated. 

9th Invest in ME conference events - IIMEC9 - are any of your health professionals going?  There is a discounted rate for medics referred by a local support group and a leaflet to download or print.

May 1st - 1 Day - £1 - 1st of the month is the day to donate just £1 to 1st class IiME research!

LIGHT UP THE NIGHT FOR ME on May 12th - can you help IiME have any public buildings in your country or area lit up blue for ME Awareness on May 12th?  Can you light your room or home blue?
International Event Page.

Turn your body blue for M.E - anyone can take part - post a photo of yourself or a body part in blue and donate to Julieann's JustGiving page. 

Selfie Facebook Fundraiser May 12th - based on the idea for cancer awareness and again, anyone can take part - post pictures of yourself on your social networking sites and donate to Clare's JustGiving page. 

Sewber Moments Online Fundraising Raffle - winners to be announced on May 12th

Sarah Mozer's Online Charity Fundraising Raffle - winners to be announced on 12th May. 

The Big Sleep for ME - now in its 3rd year and going global!  Including .. 


Poetry Competition - deadline for entries May 31st

T-shirt design competition - deadline for entries May 31st

The Princesses and M.E - their first year and what a team! Fancy being a princess for a day?

The Zzz...Factor for IiME Comedy Club - great entertainment in the comfort of your own home.

Walk for ME in its second year with the first walk for IiME already completed.

Walk for ME Isle of Man - wonderful team new on board for 2014 walking this coming weekend.

Mass Observation Diary on May 12th - for the general public in UK but an ideal opportunity to raise ME Awareness given the date. 

#May12BlogBomb - if you are a blogger or would like to write a guest blog for May 12th.

Light a Candle to Remember M.E. A poignant event created on behalf our lovely Rosa Amor.

A Vigil for International Awareness Day on May 12th in aid of Invest in ME Research, and Dr. Ian Lipkin's appeal (rituximab and microbiome research projects).

The above are group events that anyone may take part in. I
tems that Seren manages to crochet over 12 hours on the 8th May will be available for sale so you may wish to keep an eye on her Facebook page -Seren's 12hr Crochet Marathon for Invest in M.E. - She is hoping to reach her £1000 target for IiME.

Have we missed any?  Let us know!

Thank you for taking part or supporting the above.

To get in gear for May ME Awareness - visit our Shop for Biomedical ME Research - you can save £5 orders above £30 on the range of products in all the online Spreadshirt shops from 2nd to 8th May - ideal timing! Voucher code: MAY14 (cannot be used with other codes).  

Not forgetting Mama Chill's dizzyjam ME Awareness ranges with all proceeds to Invest in ME.

Click here for a variety of other ME Awareness materials.

Ready for May ME Awareness?  Let's do it for ME!


Thank you for your support. 

*Let's do it for ME! is a campaign to help raise awareness of the work of independent UK charity Invest in ME (Research) and funds for the biomedical research into myalgic encephalomyelitis that the charity is organising and/or funding. Invest in ME is run entirely by unpaid volunteers who either have ME or are parents and carers of ME patients. They are driving the agenda of scientific biomedical research into diagnostic tests and treatments for myalgic encephomyelitis in UK in collaboration with international researchers of world renown - 2014 will be an exciting year for progress in M.E. research - you can help*

Let's do it for ME!
Invest in ME (Research)
Invest in ME International Biomedical Research Conference (IIMEC)
IiME/UCL/UK rituximab trial 


POSTS

27 July 2013

Happy Birthday To Us!

UPDATE:  Click here for this post in pdf and click here for the statement by Invest in ME.

BIG THANKS to Krystal and Wobser for our birthday photo! 
The Let's do it for ME campaign was launched by a small group of people with severe ME in July 2011 in support of the proposal by innovative and forward-thinking UK-based charity Invest in ME to establish a centre of excellence for ME based in East Anglia and the first of its kind in UK/Europe, combining translational biomedical research with patient care and education and training for medical professionals, in collaboration with international researchers and like-minded ME organisations across the world. We are keen to help progress research and treatment, not only to benefit ourselves as patients, but also to avoid losing another generation to the ravages of this disease. We have no more time to lose.  We wished to assist in a practical way by raising the £100k needed to fund the foundation project to get the research strategy underway in Norwich. We were delighted to receive supportive comments for our Guest book or by other means, from some of our MPsthe Countess of Mar and Jane Colby, Executive Director of The Young ME Sufferers Trust. 

UEA foundation project fully funded
At the 8th annual Invest in ME international conference in May, Dr. Ian Gibson announced that we had reached our initial fund-raising target, which means that we had raised £100k in under two years. This is no mean feat, starting from scratch from our homes and beds, with no campaign budget or publicity.  We could not have achieved this without the tremendous efforts of a wide range of supporters, from very severely ill survivors to wonderful willing wellies. We are genuinely delighted and appreciative of any types and all levels of support, and there have been too many ingenious, innovative, creative, generous, courageous and inspiring ideas, events and contributions to mention them all individually here, some are featured in our blogs and main websites and please do let us know if you'd like yours added. 


Our Global Community
Our supporters hail from all corners of the UK, Europe, Canada, USA, Australia, NZ, and over 3500 votes in April won Invest in ME 1st prize of £2000 in The Big Break contest run by Direct Debit.  Everyone involved is a volunteer and every penny raised goes to the Biomedical ME Research.  Any competition prizes or similar resources are donated.  Members of the planning group run the campaign websites and on-line shops, organise ME Awareness events such as The Big Sleep for ME, designed to be accessible to people of all ages and levels of illness severity and launched in 2012, ongoing fundraisers such as the 1st of each month One Day-One Pound and Small Change to Change M.E, the Christmas card competition, calendars, summer quizzes, card sales, stalls, supermarket and church collections. We also proactively help to organise or support other patient initiatives that include Invest in ME, such The Big Shave 2013 and Walk for ME. This is all done painstakingly between us over the course of days, weeks, months as and when illness allows and we are ever grateful for all help and support.

BIG THANKS TO ALL 
Writer Jacqueline Rayner is a founder member of our planning goup. She had been planning with her friends and colleagues at Big Finish Productions to produce a charity audio play for download in aid of Invest in ME, based on the character of Bernice Summerfield: Many Happy Returns. Not content with that, producer Scott ran the Edinburgh Marathon for Invest in ME, writer Simon donated funds from his choir, and others working on the project have done more besides.  You can see some of these lovely people in our Bear Meets gallery on the main Let's do it for ME website. 


BIG THANKS BIG FINISH
At the same time, planning group member and writer Barnaby Eaton-Jones reworked his play, Running To Stand Still, in aid of our cause and again, everyone involved gave generously of their time and talent.  


BIG THANKS BARNABY
Music artist Mama Chill decided to proactively support Invest in ME in her awareness raising and by donating proceeds of downloads and joining the team. Her ME Awareness track is based on the original “I Can't Stand The Rain”, and her new track, “Don't Say Nuthin If It Ain't Worthwhile” was released for May Awareness. There are various other artists, writers, musicians, photographers, supporting the charity. 


BIG THANKS  MAMA CHILL
Make ME Crafts exploded onto the scene last year and is proving hugely popular, with an ever-expanding team producing an impressive range of arts and crafts available all year round.  Katie summed it up with this comment: “Big thankyou to Jon because you have brought the community together, its really positive, everyone is happy making and doing things they enjoy and its all going to hopefully find what is going on with our bodies !! Sooo happy to be a part of this XD xx” 

BIG THANKS JON AND TEAM
Another member of our planning group featured alongside an advert placed by IIME to raise awareness of the foundation research project. Rosa had previously crocheted soft wool blue awareness wristbands for IIME and her grandparents hosted a coffee morning in aid of our cause. Following a decline in her health, Rosa was moved to a nursing home, and fed by nasojejunal tube. She chose to mark her 21st birthday by raising awareness and funds for our cause. The staff at the nursing home joined in with a pyjama day with all proceeds to Rosa's appeal. Goodwill messages were posted across the social networking sites and some people used Rosa's photo as their profile picture for the day. Her mother said that the appeal passed all their expectations. Having contracted ME at 8 years of age, Rosa's story epitomises the indomitable spirit of the majority of people of all ages with ME, as well as the spirit of our campaign. 

BIG THANKS ROSA AND FAMILY
Empowerment is a key element driving the campaign and it has been very rewarding to see children and young people in particular, as well as the very severely affected, able to play a role in speaking out about their disabling illness and how it is viewed and treated by society and the medical profession, whilst taking such positive steps to raise funds for the translational biomedical research required to bring realistic hope for their recovery, with support of well friends and family members. 13-year old Harri wrote:

“Although it has been a year since I was in hospital due to M.E. I am still struggling with this awful misunderstood illness. I am still not in school and I want my life back as I knew it. I know many other children who are suffering with this illness too and I am in touch with them. They are also missing out on so many things like me. This is such a great cause, raising money to find a cure!!”

BIG THANKS HARRI AND ALL WHO SUPPORT THE YOUNG ONES

We have clearly all been very busy over the past two years, so what's next?

BIG THANKS ALL AT UEA 
The £100k raised has enabled the translational biomedical research strategy to get underway at the University of East Anglia by fully funding the foundation project on gut microbiota in ME patients.  ME is classified by the World Health Organisation as a neurological disease, but a body of research points to it as primarily a disease of the immune system with downstream effects on other systems and organs in the body and this is consistent with "encephalomyelitis" as that means inflammation of the brain and spinal cord and inflammation is an immune system response.  This could also help to account for the often fluctuating nature and variable severity of symptoms, as inflammation tends to flare and subside.  Poliomyelitis is caused by a virus that multiplies in the intestine and ME has been described as atypical or non-paralytic polio.  When Jane Colby contracted ME she was referred to microbiologist, the late Dr. Betty Dowsett, and was found to have a virus similar to the polio virus.  The majority of the immune system is in the gut and so it makes sense for a strategy aimed at finding reliable biomarkers for early and accurate diagnosis and effective treatment options to begin by looking at the gut and gut microbiota and this is an approach being taken by researchers in other countries to ME and to other diseases that affect the immune system. 

"Neuroimmune disease is very serious" 
A week after the hugely successful and productive 2013 conference, Invest in ME announced plans for a UK clinical treatment trial of Rituximab, an immune modulating monoclonal antibody used in treatment for autoimmune diseases and non-Hodgkin's lymphoma and found to result in major or overall improvement in all ME symptoms in 67% of patients in research in Norway.  This research points to ME as an autoimmune disease and even better results have been achieved in follow up studies by increasing doses to create a more prolonged effect.  Researchers in other countries now need to replicate and validate this important research, which has huge potential to increase understanding of the disease, by studying those who respond well to the drug as well as the non-responders.  Rituximab helps about 70% of patients with rheumatoid arthritis.  We are delighted that Professor Jonathan Edwards is a acting in an official capacity as Advisor to Invest in ME on all aspects of the trial as there is no-one better placed to do this, and we are now helping Invest in ME to raise the funds required for the dedicated Rituximab Research Fund, which stands at £15,000 at the time of writing.  

BIG THANKS PROFESSOR JONATHAN EDWARDS

Invest in ME has other biomedical research and related projects in the pipeline to be supported from the main Biomedical Research Fund and we will keep you posted when we have news of these to share.
The charity does a lot more besides organise and fund biomedical research and if you wish to support the other aspects of the charity's work - their campaigning, advocacy, education and awareness materials and the excellent conference events, there is a general fund you can donate to. Details and donation options are on the Invest in ME and Let's do it for ME websites.  The charity's wonderful trustees perform their work for free, ceaselessly all year round, sometimes around the clock and often under challenging circumstances, as ME sufferers or parents/carers themselves, working hard to make progress in ME research and treatment and to bring wider understanding of ME in UK into the 21st century.  What they have achieved since they formed as a group in 2005 and as a registered charity since 2006 is nothing short of miraculous.  They have done much to galvanise biomedical research into ME and we are proud to support their efforts.  

We are immensely grateful to Invest in ME and to all those who support them in their international drive to instigate, fund, and conduct the kind of high quality scientific biomedical research that may be translated into reliable diagnostic biomarkers and long-awaited effective treatment options for this organic disease and we are also extremely appreciative of  everyone who supports our campaign by raising awareness and funds in such a variety of ways.  Wherever you are based and whatever role you play, be it front of stage or behind the scenes - we thank you for your support.


Happy Birthday To Us All - Let's do it for ME!

*BIRTHDAY CELEBRATIONS NEWS*


As part of our 2nd birthday celebrations we are excited to announce 
a matching donation period for the monthly One Day One Pound event up to a maximum value of £1000 + £250 in gift aid 
from 26th July to the 2nd of August inclusive.  
The total donated will go towards the UK Rituximab Treatment Trial being organised by Invest in ME.

To donate from £1 text the code ODOP99  to 70070 
or donate from £2 via the 


The page currently stands at £2,520.22 + Gift Aid of £314.81 = Grand Total £2,835.03 so the target will be a total of £4,085.03.  When we reach that total our generous benefactor will donate the £1,000.00 plus £250.00 in gift aid.   So the Rituximab Fund will increase by a total of £2,500.00!! 

Help us celebrate our 2nd birthday by doubling your donation to this important biomedical research!

Let's do it for ME!



8 December 2012

Rosa's 21st Birthday Appeal - December Update


Rosalind Amor has been an enthusiastic supporter of the Let's do it for ME campaign since its launch in the summer of 2011, as one of the first members of the online planning group and also of the Make ME Crafts team, as in spite of severe illness, Rosa crochets soft wool blue awareness wristbands when able to for Invest in ME. We wrote about Rosa's Wristbands in March 2012 and she raised over £100 for ME Awareness Month in May but by July her hands had become too weak to crochet. Following a decline in health, Rosa spent most of August and September in hospital, transferring to a Nursing Home where she is being fed by a naso-jejunum tube.

Rosa turned 21 on 9th November and, in her usual inimitable fashion, she had a very clear idea as to how she wanted to mark this significant birthday. She planned to use her 21st as an appeal for our campaign to raise funds for biomedical ME research at the centre of excellence in Norwich proposed by Invest in ME. Rather than sending her cards and presents, Rosa asked her family and friends if they would raise awareness and money for the cause which is so dear to her heart. She had said in July, “I so wish we could get this centre running, I need it!"

For the occasion, Rosa's mother Julia prepared party bags containing a blue balloon, a LDIFME badge, ME awareness poster, leaflets and a card in which Rosa tells her story.   The staff at the nursing home joined in with a pyjama day with all proceeds to Rosa's appeal and thanks to the support and generosity of a number of people, over £1600 was raised on the Just Giving page including Gift Aid. Goodwill messages were posted across the social networking sites and some people used Rosa's photo as their profile picture for the day.  Julia said, “Rosa's Appeal has surpassed all our expectations. Check out the link to see her amazing total and all the different people who have supported her. We are so grateful to everyone.”

Invest in ME is running an advertisement in London Business Matters (LBM) for December and January, reaching 18000 people in business in London in time for Christmas and New Year. The striking ad highlights one of the research projects outlined in the proposal for the patient examination and biomedical research centre, to determine whether changes in gut microbiota contribute to ME.  First placed in October, this time the ad is supplemented with an "editorial" piece about ME and severe ME, featuring Rosa.  Invest in ME wrote on their Facebook group:

"We would like to thank Rosa for her recent appeal and Julia for agreeing to let us use Rosa's story to raise awareness.

We wish to thank all of those making huge efforts to support us and enable biomedical research into ME and thereby increasing awareness of ME.

As we have seen from recent news in Norway (no public funding granted for a Phase III trial of the promising drug Rituximab in ME patients) we, the patients and carers, will have to take control of this state of affairs and make research happen.

This is the reasoning behind our Norwich proposal - see
http://www.investinme.org/Research%20-%20ME%20Institute.htm

We are nearing our target to initiate our first project.

We will continue to progress and facilitate collaborations between researchers.

With other members of the European ME Alliance we will work together to make ME a properly researched and treated disease.

Let's Do It For ME."

Please see links for the ad below*


9th November 2012

All I want is to be like other 20 year olds; to travel and go to uni; to socialise and be independent; to walk, swim, dance and ride. I've already lost a decade of my life to this wretched illness. Please don't let me lose another.

I've had ME for 12 years. Before that, I was a healthy child. I was always playing; I loved Puppy and Kitty in my pocket sets; I went to ballet and modern dance lessons, swimming, watch club, was learning the violin and was a junior member of the RSPCA.

When I was eight my grandma and hamster died in quick succession, followed by a unknown virus of the gut. I had a terribly high temperature and was sick on everything, even water. Unfortunately, I didn't recover. I was diagnosed with ME quite quickly but sadly, this didn't make my treatment any better. I was admitted to hospital and given physio, then sent home and relapsed terribly.

I don't remember the following year. I know I lived on Complan all that time until we finally persuaded our doctors to give me a tube. I was admitted to hospital again for a few months - a painful experience.

I was paralysed and bed-ridden for 7 years and was tube-fed for 5 and a half. I remained at home, cared for by my parents. My symptoms included; paralysis especially my legs and swallow, hypersensitivity, headaches, muscle pain, 'brain fog', muteness, orthostatic intolerance, insomnia, spasms, severe nausea with a period of vomiting and extreme tiredness.

At 15 my health dramatically improved. I was able to stand and use a wheelchair. Briefly, I was even able to walk independently around the house though still needed a wheelchair outside. I became involved with my local wildlife trusts, visiting their reserves, attending 'wild learning' courses and part of a youth group.

However, from the end of 2009 my health slowly worsened again until last year, when I had a tooth infection and a bad back, I had a major crash. My worst problem this year is vomiting which worsened my tiredness, hypersensitivity, cognitive functioning and insomnia.

I always believed that one day my body would naturally heal itself and I'd return to my previous levels of health. Now I'm less confident of recovering unless someone finds a treatment.


How you can help to celebrate Rosa's 21st:

• Put up an awareness poster where lots of people will see it
• Wear the Let's do it for ME badge

How to donate:

• Online to Rosa's Justgiving Page by visiting www.justgiving.com/Rosa21

• Send a cheque payable to Invest in ME to:
Invest in ME,
PO Box 561
Eastleigh
Hampshire
SO50 0GQ
Please write 'Rosa's Appeal' on the back

• Make a direct payment to Invest in ME -
Bank: Lloyds TSB Eastleigh
Sort code 30-92-94
Account number: 02252685
Please mark your donation 'Rosa's Appeal'

To find out more about the Let's do it for ME campaign and other ways to help visit ldifme.org

To find out more about Invest in ME visit www.investinme.org

To read about Rosa's Wristbands http://blog.ldifme.org/2012/03/rosas-wristbands.html

You can read more of Rosa's experiences in her own words and including private lab tests that showed mitochondrial dysfunction on her blog  www.rosalindamorspaceofameguineapig.blogspot.com

Sending our love and every good wish to Rosa for her 21st birthday from the team at Let's do it for ME!


Thank-you for your support.

(click here for Rosa's 21st Birthday Appeal in pdf).


* Links for the ad on Invest in ME website here - :http://www.investinme.org/IIME-Newslet-Dec12-02.htm
* The Invest in ME ad is on page 51 here - http://www.londonbusinessmatters.co.uk/archive/2012-12/#/50/

* Please especially read the special supplement on page 40 here - http://www.londonbusinessmatters.co.uk/archive/2012-12/#/40/

* The jpeg of the article here - http://www.investinme.org/Documents/ME%20Awareness/LBM%20Dec2012/Invest-in-ME-Rosa-2a.jpg

* The latest ad spans December and January. The ad in Coventry & Warickshire covered November/December. The previous LBM ad was in October - so it will have had 4 months of coverage - http://www.investinme.org/medianewspapers-2012-10-01.htm


Let's do it for ME is a patient driven campaign in support of Invest in ME's proposal to establish the first UK centre of excellence dedicated to translational biomedical ME research and patient care.  All funds raised are for the research.  Please see our main website for full information and to see how you may become involved in helping to frame a future for proper recognition and treatment of this disease.

Thank-you for your support - Let's do it for ME!


For other news of our campaign please see December Updates