EPILEPSY FOUNDATION OF VICTORIA, AUSTRALIA


Four of the five members of the Walker family have epilepsy, and the youngest son Ronan also has severe developmental delay. When the Walkers went to their first epilepsy family camp, their mother Christine says it was ‘just extraordinary’. They didn’t have to apologise that Ronan was wearing a helmet to protect his head in a tonic clonic seizure, or worry in case any of the family had a seizure. They felt immediate acceptance and came away feeling part of a network of families who know what it is like to live with epilepsy.

Your donation makes our services possible, so I urge you to donate to our June Appeal. Your contribution – as much as you can afford – provides the resources that makes these services possible: camps for families, individual and family counselling services, education and training, resources and publications, research, support groups and community education.

Please make your donation and really make a difference to the lives of families like the Walker’s who ask nothing more than opportunity for their children, and understanding from the community.

Dear Ms Yin: My sincere thanks for your past support of the work of the Epilepsy Foundation of Victoria. Your generosity has made it possible for us to assist many hundreds of Victorian families and individuals whose lives are complicated by epilepsy and seizures. As we launch our major June Appeal, I am taking the liberty of asking you to commit even more generosity to our work. To make your giving easier, you can DONATE HERE securely and confidently, and help make the lives of families like the Walker's a little easier. Four of the five members of the Walker family have epilepsy, and the youngest son Ronan also has severe developmental delay. When the Walkers went on their first epilepsy family camp, their mother Christine says it was 'just extraordinary.' They didn't have to apologise that Ronan was wearing a helmet to protect his head in a tonic clonic seizure or worry in case any of the family had a seizure. They felt immediate acceptance and came away feeling part of a network of families who know what it is like to live with epilepsy. Your donation makes our services possible, so I urge you to donate to our June Appeal now. Your contribution — provides the resources that makes these services possible: camps for families, individuals and family counseling services, education and training, resources and publications, research, support groups and community education. Please make your donation today and really make a difference to the lives of families like the Walkers who ask nothing more than opportunity for their children, and understanding from the community. Thank you — we really appreciate your support. Yours sincerely
	Jeremy Maxwell For the Epilepsy Foundation of Victoria
	PS To read the full story of the Walker family, go to our website www.epinet.org.au. Please click here to make your secure donation,or telephone 03 9805 9111, and you will be assured that your donation will be tax deductible in this financial year.

TRAVEL SMART

WHEEL POWER
By ANTHONY THANASAYAN

SO you like to travel ... and you have epilepsy. That is no excuse for anyone to stay at home and avoid going to new places and meeting new people.

Serene Low, 49, from Bangsar, Kuala Lumpur, ought to know about these things. She has had nearly 100 episodes of epileptic attacks since she was a child. But that didn’t stop Serene and her family from visiting China last December.

A little slip-up made the trip an unforgettable nightmare for them.

“We were all excited about our holiday which we had been planning for months,” said Serene. “I went through our checklist twice to ensure that we had everything: passports, luggage labels, travelling itinerary, etc. “However, after breakfast on the plane, I realised to my horror that I had forgotten to bring my anti-epilepsy medication.”

All she could find was a bottle of new drug which she had never taken before. The drug was given to Serene by her neurologist who cautioned her to use it judiciously as a sudden change of medication could result in adverse side effects.

“I have not had any fits for over four years due to my daily medication. I was terrified that I might get one or several seizure attacks in China,” said Serene, an advocate for people with epilepsy. “I had no choice but to take the new drug to avoid having an attack,” said Serene.

Then it happened on the second last day of Serene’s holiday. Serene fell onto the ground at a tourist spot. Fortunately, her husband and her son were with her when it happened. They protected her head with her winter jacket and waited until the seizure had run its course. When Serene came to, she was taken to a nearby coffeeshop to rest whilst a small crowd of curious onlookers watched the whole drama. Serene later returned to her hotel room where she managed to get a good night’s rest.

Serene is thankful that she has a supportive family who are there for her all the time. Now all the wiser, Serene would like to offer the following tips to anyone who has epilepsy and likes to travel:

> Start first with your anti-epileptic medication before packing any item. And make sure you pack the right medication.

> Make an effort to recheck if someone has packed your medication for you.

> Never pack your medication into one bag to avoid not having them if your luggage gets misplaced at the airport. Have some available in your handbag and backpack as well for quick access. Carry extras in case you need them.

> Check the expiry dates of all medication.

> Always carry an identification card indicating you are a person with epilepsy, details of the type of medication you take, including dosage, who your doctor is, and important names and phone numbers to call in an emergency.

> Inform the travel guide that you are person with epilepsy so that he will be prepared to help you during an emergency.

> Mingle and get to know the people you are travelling with as a group. Share some simple information about epilepsy with them, particularly on how to help someone during a seizure.

> Stay close to your friends and family who are travelling with you.

> Keep a safe distance away from lakes, streams, fountains or waterfalls to avoid drowning during a seizure.

> Encourage your family or friends to take a video or photograph you during an attack as this provides useful material for your neurologist in treating you.

MAKING A DIFFERENCE

My blogger friend in UK told me not too long ago that he will highlight epilepsy awareness in his blog. Not only did he highlight epilepsy awareness, he also fundraised for epilepsy research by raising funds through his blog. His blog speaks volumes of himself and his philosophy in life.

My friend is Paul and he blogs as "magicdarts". Paul has raised a total of 75 pounds this month out of which 20 pounds have been allocated for www.epilepsyresearch.org.uk.

(What Paul has to say about himself)

"I'm a 39 year old family man from the East of England. Like my profile picture, the way I like to live my life is with a big smile on my face wherever possible. As of March 2010 I've decided to rename this blog Make a Difference and am going to focus all my efforts on sharing inspiring stories, and raising awareness and funds for charities that are closest to my heart - I hope you will come along for the journey!"

Please visit Paul at www.magicdartsblog.blogspot.com to read more about this fabulous, kind, warm, caring and charitable gentleman who is a fine example for anyone who wants to follow in his footsteps.

Ps. Please note that Paul also raises funds for other worthy causes. If you have any worthy personal cause/s close to your heart that you require assistance from Paul, please do not hesitate to inform Paul about it. He will be happiest to hear from you.