Hello: Hey guys and girls, im Mat. O... - Functional Neurol...

Functional Neurological Disorder - FND Hope

5,899 members3,164 posts

Hello

MatBridges profile image
11 Replies

Hey guys and girls, im Mat. O jave been diagnosed with fnd on feb this year after falling and cracking my head open on a corner of a door. Im on here to connect wirh people with the same disorder as myself and how tondeal.with it. Before this happened I was an Arborist and bodybuilder, now im trapped at home and cant do more than 30 mins of light exercise at most. Anways hello and hope to connect with likeminded people

Written by
MatBridges profile image
MatBridges
To view profiles and participate in discussions please or .
11 Replies
Brokendeer profile image
Brokendeer

Hi Mat, I consider myself to be an FND veteran now. I have the Motor FND which means my muscles do not respond correctly everytime my brain signals movement, mainly affecting my walking etc.

Now you obviously have been very physically active in your life, what with the tree work and bodybuilding and now you are unable to maintain those levels of fitness. Therefore your body is out of routine and Adrenaline levels will be random and under utilized like before.

You see I strongly believe that Motor FND is down to the brain being unable to switch off the survival response of `Flight, Freeze or Fight' due to some physical event that happened.

This means the Adrenaline that was useful before FND is now being triggered when it should not be triggered and so flooding the compromised FND brain and confusing communication/signals to the body.

Try and pace yourself with activities, emotions and especially between mental or physical tasks with frequent rest breaks and good hydration. Think about keeping that Adrenaline level stable daily would be my advice. You would be surprised at how odd things can trigger a bad attack, like simply watching an action movie for me!

Be kind to yourself, search for the calm in the storm!

MatBridges profile image
MatBridges in reply toBrokendeer

Hi Brokendeer.

Thanks for the reply. I try to limit myself and be as calm as possible. I constantly get severe anxiety attacks, usually when out in public, or wet, slippery surfaces.

For me its more affects my speech. Thank you very much for your kind words

Brokendeer profile image
Brokendeer in reply toMatBridges

Hi Mat, my friend has Speech affected by FND - they found Speech Therapy a great help, but it took about a year for the re-training to kick in!

Anxiety is one of the key problems in FND, if you have not already, give Professor Jon Stone's website a look neurosymptoms.org

You will see how common and different FND sufferers symptoms can be, and you might pick up some tips there too?

Be kind to yourself, search for the calm in the storm!

Bailey09 profile image
Bailey09

Hi Mat

I've FND now for three half years I suffer with a lot of symptoms with this disorder my anxiety is sky high at the moment plus my depression with this bloody virus at the moment I suffer with anxiety,ocd , fibromyalgia, ibs , eye migraines, depersonalizion, derealization ,balance, dizziness, speech, problems with walking and sleeping ,rls take care and keep safe x

Brokendeer profile image
Brokendeer in reply toBailey09

Hi Bailey,

I get visual migraines which I guess are similar to eye migraines, did they ever tell you what might cause them?

Like what the triggers might be to setting them off?

Any ideas would be helpful, thanks.

Be kind to yourself, search for the calm in the storm!

Bailey09 profile image
Bailey09 in reply toBrokendeer

My neurologist said stress but I've always been like that anyway x

Ottaw profile image
Ottaw in reply toBrokendeer

Did you ever had a scan of your eye? And visual Field test? If you have any inflammation behind your eye they should be able to see it. In a meanwhile there are special masks for the eyes you could purchase at the pharmacy, then you place it in the microwave for a second and then place the mask over your eyes it will ease the pain.

Brokendeer profile image
Brokendeer in reply toOttaw

Hi Although I have never had an eye scan, I do have a fantastic optician who looks after my eye health. The Visual Migraines are sudden, so maybe a warm eye mask may help at that point in time - always assumed there was nothing I could do but wait for it to pass? Like Bailey, I have always been anxious/stressed and suffered these eye problems, even before FND.

Thanks for your advice though,

Be kind to yourself, search for the calm in the storm!

Ottaw profile image
Ottaw in reply toBrokendeer

Happy to help.

tabey profile image
tabey

Welcome to the clan mat

MatBridges profile image
MatBridges

Hello thanks to for being so kind

Not what you're looking for?

You may also like...

Hello! Newbie here :)

My name is Tam and today I've been diagnosed with FND. I am almost 35. I live in Australia with my...
Tam81 profile image

Hello wonderful people ❤

Hi everyone Im Dana! Im new to this page/group. However have been living with my diagnosis which is...
Arlie_22 profile image

Hello

Hello, I was diagnosed with FND in February after having several stroke-like episodes. My 2 main...
IceOwl profile image

Hello

Hi there, this is my first post and I am not sure of where I should start. I feel very alone these...
mavem100 profile image

Fnd flare ups

Hi guys i hope this is the right place im posting on, its took me nearly 3 yrs to actualy write on...
Dinky12 profile image

Moderation team

See all
FND_ profile image
FND_Administrator
hope4fnd profile image
hope4fndModerator
DNE92 profile image
DNE92Moderator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.