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A list of frequently asked questions for fundraising
They are several ways which you can send us the money you raised. You can send a cheque to us and you can make a bank transfer or donate via the website. Please don’t send cash to us, if you choose to please hand this in directly into our head office.
You can go via our website and click on the donate tab to choose which project you would like to donate to.
Ataxia UK is entirely funded by the money we raise. Some of it comes from trusts and grants, but most of it comes from the generosity of people like you, who make donations, raise money, and leave us gifts in their wills. For information on any aspect of fundraising or tips and support contact the Fundraising team on 020 7582 1444 or [email protected]
Yes, we provide a range of exciting merchandise that can be used to fundraise and increase awareness of Ataxia UK.
If you are a UK tax payer you can increase the value of your gift to Ataxia UK, at no extra cost. By signing a Gift Aid Declaration, with your permission, the Inland revenue allows us to claim an extra 25p for every pond you donate.
We’re thrilled you want to fundraise for us. They are so many ways you can get involved- why not take a look at our events page for some inspiration.
Ataxia with oculomotor apraxia (AOA) comes in two forms, AOA1 or AOA2. They make two of the rarest types of ataxia.
Dentatorubral pallidoluysian atrophy (DRPLA) is a type of inherited progressive late-onset cerebellar ataxia. It is characterised by a defect in a gene that causes damage to a certain part of the brain, the cerebellum.
Strokes, gluten intolereance, alcohol, vitamin-E deficiency and trauma to the head can all cause ataxia. Some of these types can be reversed, depending on the cause; a vitamin-E deficiency can be reduced by attention given to diet, for example, that will reduce ataxic symptoms and in some cases, eliminate them all together. A patient must consult their GP or neurologist before attempting to make any changes to their diet.
Idiopathic ataxia is the name we give a type of ataxia for which the cause is not yet known. Almost 50% of people with the condition have idiopathic ataxia, showing just how much more work there is to do.
Gluten ataxia is caused by a sensitivity to the protein gluten found in wheat products. It is one of the most common forms of sporadic idiopathic ataxia (where ataxia is found in people with no family history of ataxia and no known cause). You can find more information on Gluten ataxia research here.
Our specialist ataxia neurologist, Professor M Hadjivassiliou, is a leading expert in gluten ataxia. He runs the Specialist Ataxia Centre in Sheffield, and is leading research into the condition. If you have a diagnosis of gluten ataxia, please ask for a referral from your GP to the centre for specialist care. You can read how to do that here.
There is also a useful app that helps to monitor the gluten content in well-known products, assisting with your shopping and taking control over your condition.
Episodic ataxia is characterised as bouts or attacks of ataxia symptoms. The episodic ataxias are a relatively rare group of conditions which, as their name suggests, tend to affect people in bouts or attacks of unsteadiness. There are several types, but type 2 are the most well understood, and they are called episodic ataxia type 1 and 2. Both of these occur in families and are inherited in what is known as an autosomal dominant manner. This means that an affected individual has a 50% chance of passing the gene on to their children.
You can read more about the episodic ataxias here.
The Spinocerebellar ataxias (also called SCA's) are caused by mutations in different genes. For example, spinocerebellar ataxia 1 is linked to a default in the gene SCA1.
Through research, more than 100 types of SCA's have been discovered since 1965. For more information on the different types of Spinocerebellar ataxias, see below:
Spinocerebellar ataxia 1 (SCA1)
Spinocerebellar ataxia 2 (SCA2)
Spinocerebellar ataxia 3 (SCA3)
Spinocerebellar ataxia 6 (SCA6)You can also view an illustrated leaflet on SCA6 kindly provided by Health Press Limited.
Spinocerebellar ataxia 7 (SCA7)
Spinocerebellar ataxia 11 (SCA11)
Friedreich's ataxia is the most common form of hereditary ataxia, and is caused by an inherited mutation in the frataxin (FXN) gene. See our information booklet for more information:
As well as becoming a Friend of Ataxia UK, we encourage anyone with a diagnosis of Friedreich's ataxia to join the FA Global Patient Registry.
Our meetings take place at 11am at The Deal Centre for the Retired, 3 Park Street, Deal, Kent. Get in touch with Christine to come along.
Jean Gillard [email protected]
Our meetings take place at The Roller Mill, Mill Lane, Uckfield TN22 5AA - please contact Jean for more information!
Vanessa Bartlett [email protected] 07701 007 825
Yvette Loach [email protected] 07738 366 433
Dawn Wooldridge [email protected] 01268 545 584 or 07539 061 075
Derek Wood [email protected] Mobile 07776 188 877
Stewart Smith07759 539 987[email protected]
Our 2020 meeting dates are: 21st January, 18th February, 24th March, 28th April, 26th May, 23rd June, 21st July, 18th August, 22nd September, 20th October, 17th November and the 15th December.
Tim Flanders[email protected] 07792 718178See the latest going on here
Jennifer Davies[email protected]
We welcome new members, please contact Jennifer for more information.
Barry Munday01279 843 687[email protected]
See our website here
Meetings take place in the Beefeater at the Premier Inn, Marsh Lane, Ware SG12 9QB. Please contact Barry for dates and times of meetings.
David Stubley01205 722 771 [email protected]
Read our latest newsletter here