rebecca Rogers

March Walking Challenge

Thank you for visiting my fundraising page!

This March, I'm walking and raising funds to support people living with epilepsy, and their families.

Epilepsy is characterised by a discharge of electrical energy in the brain, but the way this affects each person is unique. With your help, Epilepsy Ireland can provide support tailored to the needs of each person and family living with epilepsy.

Your support will ensure that people with epilepsy and their families receive the information, advice, and support they need through a network of 11 Community Resource Officers. You will ensure public awareness of epilepsy is improved and stigma and misunderstanding is alleviated. You will help fund vital research projects to find new ways to manage and treat epilepsy and reduce its impact on people’s lives.

I hope you can help me by making a donation. Simply click the Donate button. All donations are processed securely and are received directly by Epilepsy Ireland.

My Achievements

Fundraising page

Donated to Own Page

Updated Profile Pic

Added a Blog Post

50% of fundraising goal

Reached Goal

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My Updates

The beginning of Cians journey

Monday 9th Feb
Cian was 3 years old when he first had a seizure. In August 2022 he had a tonic clonic we as parents did not know what had happened and weren’t there either, he was rushed to the hospital and we were told that a child/adult could have 1 seizure in their life without a reason he was discharged and let home and exactly a month later september 2022 he had 4 tonic clonics within 7 minutes. He was giving the Diagnosis of Epilepsy and put on Keppra. 5 Months seizure free and unfortunately Cian had another tonic clonic in February 2023 which than the looked at his medication and changed it. From February 2023 to November 2025 Cian suffered Multiple different types of seizures including both generalised and focal epilepsy and was given the Diagnosis of Drug Resistant epilepsy. Cian has been trialed on multiple medications throughout his journey trying to find ones that suits his epilepsy. Cians also had Steven Johnson Syndrome ( reaction to anti epileptic medication). He unfortunately has had pneumonia aswell. He has had blood work sent to dublin an spent a week in Temple Street. Throughout Cians journey we seen our little happy boy go from the most out going person to the life been sucked out of him. Epilepsy has taken so much away from our boy. His walk was and has been affected and speech. 
We are currently 2 months seizure and it’s the longest we have been in a very long time. 
Thank you all for your kind donations 💜

Thank you to my Sponsors

100

Little Stars Athenry

👍

53.42

Cathal Page

50

Ellie Hickey

40

Angela Joyce

37.53

Chami Johnson

37.53

Sarah Talty

26.98

Shauna O’connell

21.86

Paddy

21.86

Jessica Cunningham

21.86

Brandon

21.86

Brían

21.38

Lizzie

17

Nana Brehony

Little warrior

11.24

Sarah Costello

11.24

Thomas Fleet

Good man Cian.

11.24

Rebecca Rogers

11.24

Laura Cooney

11.24

Shannon Elbert

10

Bakie

🤍

10

Sandra Noone

Best of Luck Becca, Cian is a very lucky little boy to have you advocate on his behalf!

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