@albiongirl68@WendyPMitchell Thank you Julie! Yes I do and I have also inherited the genetic mutation. If Professor Pat wants to ask any questions I am available! ☺️
US approves first new #Alzheimer's drug in 20 years... this is absolutely incredible to read! Progress for so many and amazing to see @cathmummery from the very same research centre I was at last week speak about it! Well done to all involved ♥️♥️ https://t.co/N5wI0hKnJY
It’s #DementiaActionWeek and I’m starting by sharing a podcast I recorded with @JillRennieuk at @homecare_co_uk. This explains my own experience with #FTD after my mum was diagnosed, and after I tested positive for the #C9ORF72 mutation. Click to listen! > https://t.co/hUe9SQ8Unz
It’s here! Check out my interview on @RadioHumberside speaking all things #ftd and how I’m dealing with my #genetic results. Earlier on in the show, there’s also great info from @LucyL_Russell and @Hannahdementia! Check it out at 2:41:00 👇🏼 https://t.co/GQhdMe5rI2
Thank you so much @Hannahdementia for your involvement! You did amazing and provided such insightful info. We were a fab team! #ftd#endftd https://t.co/8yXZLQjNzu
I had my first live interview on BBC radio Humberside this morning helping to share the story of @FTDandMe. Jess, you are such a brave woman and an inspiration to us all at @FTDtalk, thank you! #ftd#c9orf72
@LucyL_Russell@FTDtalk Thank you so much Lucy! I am so happy that you got involved, the more people that know about your amazing research, the more people will get involved! You all do such amazing work, thank you for supporting me! You did AMAZING! #ftd#endftd
I visited mum in the care home on Saturday morning. It was the first time I've seen her properly in 2 months and it was hard. Lots had changed and there is so much I wish I had done differently. Tips for the future listed below 👇🏼 #ftd#endftd#dementia#dementiaawareness
Will I inherit FTD? I published a blog about late last night about waiting for the results regarding my own #genetic testing, hopefully it will give those in a similar situation some useful information 💕 #FTD#FrontotemporalDementia https://t.co/E14IajTUty
There is one simple aim with this: Connect young adults who support their parents living with dementia, to enable them to learn and support each other and just have a chat with a mate who “gets it” over their preferred drink of choice ☕️🍷🍻
Started a new thing 👋 Launching a new group for the young adult children (18 - 35) of those living with young onset dementia.
We’re starting small and have a fledgling Instagram account here:
https://t.co/s8gaJVUbju
Please share / RT ❤️
Time for #Blog #14. I’m talking about the present and I’ve explained how mums symptoms have changed. I found it hard writing this, it was a complete reality check. I can’t believe how quickly things have changed 😢♥️ #FTD#FrontotemporalDementia#Dementia https://t.co/ae21Oe88M7
Morning Twitter! It’s time for another blog 🎉 This story brings back outrageous but hilarious memories for me. Have a read to see how life continued after mums #FTD diagnosis! #Dementia#EndFTD#FrontotemporalDementia#Blogger https://t.co/qTzhoKr95l
I love how this chart shows the many different conditions which sit under the umbrella term ‘dementia’. So many need awareness raising! #Dementia#FTD#EndFTD
I’m back! My next blog is now published which covers how we received a diagnosis. I’ve had lots of questions about this so hopefully you’ll find it useful. Enjoy and I hope to continue shining a light on #FTD! #Dementia#EndFTD#FrontotemporalDementia https://t.co/cYJmEbdUc5
Feeling so loved it’s unreal 🥰 I have created my own @alzheimerssoc Memory Walk to take place on 20th September 2020. In just 18 hours I’ve got 25 walkers and raised £210! So thankful to those who have supported me so far ���️ #Dementia #EndDementia https://t.co/67l9GRzNnO