FND FIGHTERS

On a mission to provide more funding, more answers and more care for those suffering from FND.

[FND FIGHTERS @FightersFnd]

Our logo. The ‘F’ is crossed out to portray our mission to eradicate the notion that #FND is just a ‘psychological condition’. It also emphasises our (and many others) belief that there is in fact a structural defect (however small) causing the symptoms of FND patients.

[Matthew Newsham @MatthewFND]

New Blog alert!!! https://t.co/Y2wxdCMRiE
@FNDHopeUK @FNDAction #FND #fndmen #Family #FNDWarrior

[FND FIGHTERS @FightersFnd]

Inspiring 💪🏻

[Matt Hampson @Hambofoundation]

Just wanted to share Katie’s incredible progress over the last few months. You all probably know from my previous posts that Katie, suffers from FND (Functional Neurological Disorder) Videos, on the left, are from a few months ago. The videos on the right are from last week #FND

[FND FIGHTERS @FightersFnd]

Hey everyone, here’s my latest vlog.

Talking about receiving the FND diagnosis after 4 months, and how I’ve restored a small sense of normality to daily life. #FND

https://t.co/AYW8C5nVMo

[Matthew Newsham @MatthewFND]

Here is the next #blog post as promised. This one looks at #family and #fnd
@jonstoneneuro @Tim_R_Nicholson
@FNDHopeUK
https://t.co/Ua71i5JMKC

[FND FIGHTERS @FightersFnd]

@warewendy_ware Hey Wendy. So sorry to hear that. Please don’t lose hope on her getting better though, I’ve seen some amazing turnarounds. I hope, pray and believe your daughter can too

[Wendy Ware @warewendy_ware]

Despite a diagnosis of FND our daughter remains unable to eat, experiences migraines, NEAD, widespread pain and requires a wheelchair. She was a neonatal nurse until 4 years ago. When will the NHS wake up?

[FND FIGHTERS @FightersFnd]

@KeynshamAction Thank you very much

[FND FIGHTERS @FightersFnd]

My new vlog on my #FND progress, symptoms and doing what I can to help raise awareness

https://t.co/YMaigurQeu

[Hannah Deakin @HannahEDeakin]

NEW BLOG POST: My stay at the wolfson unit

'It is a great place which has certainly had a positive impact on my life.'

@FNDHopeUK @FNDAction @FightersFnd @BloggingBed #DisabledBloggers #fnd #queenmaryshospital

https://t.co/8FRoeyzDYu

[FND FIGHTERS @FightersFnd]

@megjacks_ @FndPortal @FndLifewith Congrats! For the record.... I thoroughly enjoyed your ultrasound joke 😂

[FND FIGHTERS @FightersFnd]

Early designs for merchandise available from our website. 100% of profits will go towards funding help for FND sufferers. We will strive to provide free access to CBD oil for starters.

[FND FIGHTERS @FightersFnd]

@ShelleyIOWUK In the meantime (if you aren’t already) join the group on Facebook ‘Functional Neurological Disorder’ everyone on there has been really helpful and supportive.

[FND FIGHTERS @FightersFnd]

Fellow #FND sufferers! I am in the process of developing our website. What tools, tips and content do you wish you had at your finger tips to help with your symptoms and feelings?

[FND FIGHTERS @FightersFnd]

@ShelleyIOWUK I will put together an extensive list of known symptoms and have an interactive feature where people can mark whether it is a symptom they’ve experienced and perhaps the duration (days) it has gone on for (at one time) Would that help/ reassure you? I know the feeling by the way!

[FND FIGHTERS @FightersFnd]

https://t.co/eNX6QacSbr This is interesting. #FND

[FND FIGHTERS @FightersFnd]

If only....

[FND FIGHTERS @FightersFnd]

Research in four major neurological centre suggests about 1 in 3 people attending #neurology outpatient clinics are diagnosed with #FND. How can CCGS and STPs justify not having dedicated FND services/support across the entire country?

[FND FIGHTERS @FightersFnd]

@MatthewNewsham1 Rest up mate, hope you’re feeling better soon.

[FND FIGHTERS @FightersFnd]

Look forward to seeing how useful this is