A tender lady’s go back and forth to the clinic for 4 days of exams changed into a two 12 months fight which left her paralysed and fearing she might by no means be capable to talk once more.
Megan Dixon used to be 13 years outdated when she started to really feel sick.
By age 16 her well being had deteriorated to such an extent that she had misplaced the power to talk.
She used to be taken to clinic for exams that have been simplest meant to take 4 days, docs believed {the teenager} could have suffered a stroke.
Two years later she used to be totally paralysed. Unable to stroll, communicate or open her eyes, with docs pronouncing she might by no means transfer once more.
Megan used to be identified with Functional Neurological Disorder (FND), a situation which affected how her mind gained and despatched knowledge to the remainder of the frame.
Megan advised BBC News that the situation left her not able to speak or do anything else for herself.
‘I could not see, so I wasn’t in a position to open my eyes. My mind could not sign up the adaptation between eyes closed and eyes being open,’ she added.
Megan Dixon used to be left paralysed and not able to talk after being taken into clinic when she used to be 16

Now elderly 20, she is sharing her stories of FND on her TikTok account

Megan is now in a position to face however calls for a large number of enhance and will simplest set up a couple of steps
At the age of 18, Megan used to be moved from the clinic in Bath to a neurological care house in Peterborough to obtain the care she wanted.
Megan mentioned she used to be ‘only a child’ on the time and had by no means been on her personal sooner than.
‘It used to be now not simple. I believe it used to be so much tougher for my mom and dad to have to depart me there by myself, however I could not do anything else for myself. I used to be paralysed from the neck down,’ she mentioned.
Megan mentioned her situation began off slowly when she used to be 13 however she started to become worse all of a sudden in 2021.
She misplaced the power to swallow and used to be fed through a feeding tube in her mouth, which has been changed through one immediately into her abdomen.
At one level she used to be having 50 seizures an afternoon, however that has now been decreased to between 10 and 15.
Now elderly 20, and after 18 months of intensive treatment, Megan is making ready to transport into her own residence and hopes to grow to be a nail technician.
Her lifestyles has modified dramatically and she will now communicate and transfer through herself.

Megan Dixon feared she would by no means go away the clinic, together with her folks advised to ‘get ready for the worst’

Megan now hopes she is going to be capable to transfer into a house together with her boyfriend Oli

After believing she might by no means go away the clinic, Megan is making plans to take a direction to grow to be a nail technician
She has contractions in her knees, that means she is not able to bend them, leaving her legs caught immediately. It manner she is going to by no means stroll once more.
Megan mentioned she by no means anticipated that she would be capable to plan a lifestyles out of doors of the clinic.
She mentioned her frame close down such a lot that she just about died in clinic.
She mentioned: ‘The docs did have to inform my folks to organize for the worst – they did not assume I might make it to 18 and right here I’m at 20.’
Megan is now saving up cash to take an internet direction to grow to be a nail technician.
She is taking a look to transport out and discover a house together with her boyfriend Oli.
Megan now stocks her stories of the situation on TikTok.
On her account she has shared herself the use of a wheelchair for the primary time and the way she used to be in a position to stroll for the primary time in a swimming pool.
One video presentations her the use of the steps for the primary time in over 3 years, the use of her fingers to tug herself up and decrease herself down once more.
She mentioned that every now and then she were left remoted, annoyed and exhausted because of how ‘unpredictable’ lifestyles with FND were.
Now she says each small victory similar to transferring a finger or talking a phrase is ‘price celebrating’.