Rezultati pretraživanja
  1. 29. lip 2019.

    Hey guys Check this video out if you wanna know a little about my disorder and why I use a walker!

  2. 6. svi 2019.

    I am a founding member too! Seeing all these founding women reminds me of Abigail Adams letters to the Founding Fathers. Excited to collaborate with all in the Functional Neurological Disorders Society

  3. 16. svi 2019.

    Anyone can suffer from a functional neurological disorder, they're real and great medical help is available

  4. 2. lis 2018.

    A HUGE thank you to those involved in 3 events, in 3 countries, for FND Hope. We raised the following: £6,650.83 (GBP) $11,064.92 (CAD) $12,006.79 (AUD). Together, with hope, we can help make a brighter future for all FND fighters!

  5. 9. svi 2019.

    Masterclass was packed with information and great speakers today! Thank you . There are more and more charities supporting people with FND in the UK! and

  6. 12. kol 2019.

    Another reason that and is possible. He called me mom this morning, without any reminders or clues. He knew who I was when he saw me in the morning for the first time in months.

  7. 23. lis 2019.

    Looking for the lost core. Anyone seen those neural pathways he lost 3 years ago.

  8. We're glowing orange and blue tonight for World FND Week 🧡💙 Functional Neurological Disorder (FND) is a disconnect in the nervous system and affects how the brain and body send and receive signals. Learn how you can be at

  9. 30. sij

    1st check in with my neuro in over a year. Good news is I still have a few operating brain cells in there.🤪The bad news is there’s still no cure for . So I’ll keep fighting, keep raising awareness, & keep on keeping on.

  10. 30. sij

    A year ago I was finally diagnosed after 5 years of countless amounts of doctors, specialists, scans and tests There needs to be so much more awareness of this illness that affects so many 🙄

  11. 19. sij

    Hi Mike. It's been a while. Hope that you have rested well and recovered from the fight when you stood in our corner. Valiently. Thank you.

  12. 25. stu 2019.

    Mike is making a difference as he supports for his fight Plz and thanks Raising Awareness for

  13. 24. stu 2019.

    The amazing supported for his fight. He is a family friend, who wanted to help spread awareness for FND. Pls follow to thank him for using his platform for good. He is a big guy with a kind heart.

  14. 🥊 TONIGHT, LIVE ON CHANNEL 5 GMT 🥊 fighter Mike “Seabass” Shipman has chosen FND Hope as his charity, for his fight against Fabian Edwards at the Wembley - Come on you can do it! 👊🏼

  15. BELLATOR MMA fighter chose as his charity, for his fight on 23rd November at SSE Arena, Wembley. Please show your support for Mike in WINNING the fight! ⭐️Please LIKE & RETWEET⭐️

  16. 12. lis 2019.

    I want to prove that ANYTHING is possible - by not only relearning to skip, but also become Ellen’s elf! Please support me in my journey and subscribe and share my YouTube channel 😘 x

  17. My next blog post about life with FND. Please feel free to share xxx

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  18. 2. ruj 2019.

    People who know me will know how much this has changed my life. I've been lucky with an early diagnosis and treatment from the but my life is still so different to how it used to be.

  19. 13. tra 2019.

    Warrior Nick Manely finds activities to help him fight FND. the first his love for Skiing and has also picked up art, with many pieces being sent internationally

  20. 13. tra 2019.

    🧠 Final Day (7) of World FND Week Being stuck in a body you can’t recognise is more than upsetting. Please help give the patients in neuro rehab, a manicure or pedicure. All donations, however small, will all be so helpful

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