@MorbidKnowledge I was diagnosed with FND 6 years ago and I still have to use a wheelchair. Well done to this girl for getting well twice. I've never heard of the steps centre in Sheffield. I'll have to look into it.
We're inviting the Jack Army to take part in a pop up ‘fan museum’ on June 13 as the club marks its 114th anniversary with the unveiling of a brand new International Honours board created by @swanstrust 🦢
👉 https://t.co/QLMGpWUzeB
@brutalfightz2 He's being smart here. Gathering evidence. I hope he took the child and left her. She absolutely doesn't deserve to be a mother. People out there who would love to be parents and then you get this piece of shit?? Wheres the sense?? I hope that baby is far away from her now.
@IgracBarake@brutalfightz2 He's being smart here. Gathering evidence. I hope he took the child and left her. She absolutely doesn't deserve to be a mother. People out there who would love to be parents and then you get this piece of shit?? Wheres the sense?? I hope that baby is far away from her now.
@SirshoaibS@SwanseaCouncil@swpolice Some of the comments on here are absolutely disgusting. He is a father and wants to protect his daughter. What's wrong with that?
@TheGriftReport She may be able to qualify for free NHS ambulance transport. It's a non emergency ambulance that takes patients to appointments. I use them for my dialysis treatments 3 times a week.
@mrwtffacts Her fingers look like dystonia. It's a crippling symptom of FND...which is neurological. I've had it for 6 years now and my hands and arms go into weird and painful positions sometimes. I'm not a doctor and not diagnosing her....but I'm just saying what her hands look like.
21 monuments in Canada will be lighting up the sky bleu and orange for #FND awareness in support of the tens of thousands of children and adults impacted by Functional Neurological Disorder across the country.
#FNDaware