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What's your disability?

User Profile: Evois
Evois June 7th, 2016

I have a learning disability.

What is the most difficult part of your disability?
For me its being slow when my brain sometimes either moves toooo fast or not fast enough and I have to take longer on stuff.

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User Profile: japarker
japarker August 9th, 2019

I have Macular Degeneration, PTSD, Autism Spectrum Disorder, Anxiety, Depression, OCD, Peptic Esophagitis Disease, and Fetal Alcohol Syndrome.

User Profile: No715
No715 August 17th, 2019

Hi everyone!

I have Anxiety, PTSD, Depression, Asthma that is triggered by allergies, and a CHD.

User Profile: FunkyFlamingo
FunkyFlamingo September 1st, 2019

Outside of mental health issues that greatly interfere with my life. My disabilities include...

- Tachycardia w/ PVCs

- Restrictive Lung Disease

- Gastroparesis

- Severly Delayed Colonic Transit

- GERD & Regurgitation issues

- Endometriosis

- Polycystic Ovary Syndrome (PCOS)

- Pelvic Pain

- Pelvic Floor Pain

- Pelvic Floor Dysfunction

- Suspected Adenmyosis

- Vulvadonyia

- Intersistital Cystits

- Neuopathy of legs

- Neuropathy of arm

- Encephalopathy

- Failed Back Syndrome

- Exposed Nerve in back

- Spinal Stenosis

- Herniated discs

- Degenerative Disc Disease of entire spine

coolfrownblushlaugh

User Profile: piecefulzen
piecefulzen September 1st, 2019

anxiety, depression, OCD

User Profile: BabyHedgehog0520
BabyHedgehog0520 September 6th, 2019

I have extreme social anxiety, an extreme speech impairment (which causes me to be bullied and pushed around a lot), and I have POTS.

3 replies
User Profile: GrowingGinkgo8847
GrowingGinkgo8847 September 12th, 2019

@BabyHedgehog0520

heya what speech impairment do you have? I stutter and it caused a lot of childhood suffering because I didnt know how to cope.. actually I still struggle quite a bit but Im working on finding acceptance. People still bully me at times as an adult just in a different way... I realize I can only control how I react to other people and cannot control them but its so dang hard.

2 replies
User Profile: BabyHedgehog0520
BabyHedgehog0520 September 12th, 2019

@pinkWriter8847 I stutter too. It is super annoying because people seem to really really really get enjoyment from mocking me. And it is so embarrassing sometimes.

1 reply
User Profile: GrowingGinkgo8847
GrowingGinkgo8847 September 13th, 2019

@BabyHedgehog0520 Are you in any support groups for people who stutter? If you're in the USA there is the National Stuttering Association (NSA) where I found invaluable support through a local chapter. There are different organizations around the world too if you're based somewhere else. Feel free to message me if you want to talk. It helps me so much to talk to people who actually "get" stuttering. Hang in there and know you are not alone!

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User Profile: PurpleYogi6891
PurpleYogi6891 September 6th, 2019

I have scoliosis (have had rod placement surgery and then removal surgery due to osteomyelitis), due to scoliosis I also have a leg descrepancy, rib hump and skapular diskenesis. I have spinal osteo arthritis, postural orthostatic tachycardia, idiopathic hypersomnia, gastroparesis, pcos, adenomyosis, seborrheic dermatitis (I'm losing my hair at the moment), polymorphic light eruption and oral allergy syndrome. I have battled MRSA, staph and corynebacterium infections. I'm allergic to a few antibiotics and pain meds. Also allergic to stitches, all animals and grass, pollen, hay, dust, dust mites and mold. I have anxiety, depression and PTSD. With a lot of work, I've shifted my mindset and managed to not let all of this overpower my life. I now focus on yoga and natural supplements and eat as healthy as I can. 😊

User Profile: sincereOcean4592
sincereOcean4592 September 6th, 2019

I have relapsing polychondritis, but with that, or because of that, I have Eustachian tube dysfunction, Tachy-Brady Syndrome, Afib, Diverticulitis, Vestibular dysfunction...probably more lol

User Profile: astralie
astralie September 27th, 2019

I have a spinal cord injury (SCI)

Its a complete injury/ASIA A which means no messages to/from the brain can get past it, it's a C5, C6 and C7 injury which are the cervical vertabrae 5, 6 and 7 down in the neck.

I pretty much can only move/feel bits of my arms (basically nothing in my hands or triceps) and my head/neck.

I use a power chair for getting around usually when out but I have a manual I use at home and sometimes at school.

I also have a caretaker/aide to help me do things such as get in/out of bed and get dressed.

1 reply
User Profile: adventurousBranch3786
adventurousBranch3786 September 28th, 2019

@astralie Hi, it's nice to meet you. It sounds like you have a lot to deal with. It's great that you are attending school in power chair or regular wheelchair. How are things going for you at school?

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User Profile: Zebra15
Zebra15 September 28th, 2019

I have hypermobile ehlers danlos syndrome, gastroparesis, and postural orthostatic tachycardia syndrome

User Profile: astralie
astralie September 29th, 2019

@adventurousBranch3786 It's going good mostly. Currently have a lot of math work to do which is hard when you can only type but that's fine.

I have a lot of projects to do as well but I've been working on them.

3 replies
User Profile: adventurousBranch3786
adventurousBranch3786 September 29th, 2019

@astralie Best of luck to you in your studies (especially math). I hope to see you here at disability community.

2 replies
User Profile: astralie
astralie September 30th, 2019

@adventurousBranch3786

Thanks, I'll try be active but it can be quite tiring with my arms

1 reply
User Profile: adventurousBranch3786
adventurousBranch3786 September 30th, 2019

@astralie That's okay too. I understand.

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