Skip to content

Campaign For My Brain

Turning Fear Into Hope
  • About Us
  • Meet The Campaigners
    • Meet Emma
    • Meet Kelly
    • Meet Catrin
  • Blog
  • Jenny: Life in HD
  • Useful Resources
  • LIVE Change.org Petition

Blog

A Carer’s Guide to COVID19

March 23, 2020 campaignformybrain Leave a comment

Firstly…. What a whirlwind few weeks! I don’t know about anyone else, but I am scared. I try not to…

Continue Reading →

National Young Carers Awareness Day 2020

January 30, 2020 campaignformybrain 3 Comments

It’s a day dedicated to recognising the little super hero’s holding families together in tough times. Below are the winners…

Continue Reading →

“Our life in HD – family of 3…”

campaignformybrain Leave a comment

This is the beautiful blog post written by a lady, watching her husband change with Huntington’s disease. They have a…

Continue Reading →

VACANCY: Unpaid Carer. 365 days a year. 24/7 on call.

January 21, 2020 campaignformybrain 1 Comment

Written for my Dad. By Emma Terranova Davis, Co-Director and Founder of CFMB not for profit Ltd. I have brand…

Continue Reading →

My Huntington’s Journey: by Jami, 26, North Carolina.

November 15, 2019 campaignformybrain 1 Comment

My dad passed away my senior year of high school. We didn’t have a relationship. The same semester, I was…

Continue Reading →

‘A-O-K’. Accept. Adapt. Overcome. KICK-ASS.

October 3, 2019 campaignformybrain 12 Comments

The last few blogs have been a little bleak to say the least! Today I wanted to post something a…

Continue Reading →

Our Shining Star

September 28, 2019 campaignformybrain 4 Comments

NB: If you’re reading this on a smart phone, it may look easier to read by turning your phone horizontal)…

Continue Reading →

Knock Knock.. Who’s there? Huntington’s Disease. It’s time to grow up, you’re a carer now…

July 5, 2019 campaignformybrain 39 Comments

One day I’m sneaking out of my friend’s with her to meet boys and drink WKD (Yes I really was…

Continue Reading →

Progressive Supra Nuclear Palsy (PSP): Life with PSP

April 7, 2019 campaignformybrain Leave a comment

Welcome to this honest, heart warming blog post from a follower called Rachel, who has written about her Dad, who…

Continue Reading →

Jacqui, 53. HD-

March 26, 2019 campaignformybrain 1 Comment

Jacqui is the creator of ‘Sybil on Tour’ which raises money for the Huntington’s Disease Youth Organisation. Follow her on:…

Continue Reading →

Post navigation

Page 1 of 3
1 2 3 Next →

Emma @campaignformybrain

  • Email
    campaignformybrain@gmail.com

Thanks for supporting!

Copyright © 2021 Campaign For My Brain — Lyrical WordPress theme by GoDaddy