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"I have a disability, but my disability doesn't have me"

User Profile: Emily619
Emily619 March 26th, 2017

Hey guys! I originally saw this line from a Member of TSA-USA (Tourette's Syndrome Association of The United States of America) as I read their articles from time to time since I personally deal with Tourette's too. I think this can be applied to disabilities as well smiley So, how have you overcame your disability? If you haven't, how do you plan to do so? What are some things your disability won't steal from you? Positive answers only please so we can create a positive and supportive environment heart

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User Profile: AffyAvo
AffyAvo March 27th, 2017

I'm trying to find ways to hopefully reduce symptoms more as they still get in the way of many things. I have learned how to deal with my attacks - those could lead to a hault of most other things when they hit.

While my illnesses have altered some things it doesn't mean they are ruined - I have so much fun watching all the new things my nephew has learned, my husband and I love each other and I read up on things to learn about them.

User Profile: ItsPreeti
ItsPreeti April 2nd, 2017

My views on resolving disability click the sparkling Pink - Hi

My question do we have any type of disability. It's just that we are more specially abled.

User Profile: AutumnLeigh
AutumnLeigh April 4th, 2017

I have Multiple Sclerosis. When it was finally diagnosed, I was in a wheelchair and in and out of nursing homes feeling helpless and useless. Now, 15 years later, I've learned SO many things. I've learned I have a place in this world that is productive. I've learned patience and empathy. I've learned that I don't have 'struggles' so much as I have 'challenges'. I've learned how to cope, be healthy and push my limits. I've left my wheelchair in the dust and with help, live independently and take care of my 'family' of cats. I have Multiple Sclerosis, but M.S.- you will NEVER have me! heart

2 replies
User Profile: ItsPreeti
ItsPreeti April 4th, 2017

@AutumnLeigh, I love your spirit and you have a long way ahead. MS will never have you smiley.

1 reply
User Profile: AutumnLeigh
AutumnLeigh April 4th, 2017

@JovialOne

You are incredibly supportive and amazing! Thank you for being here and sharing!! laugh

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User Profile: Xotamato
Xotamato April 4th, 2017

Physical convulsions from anxiety can leave me feeling like I just don't have a shred of control over my own body. My neurologist trying to help me understand. You know what? She cares, the people in my life, they care. She tries to explain so that I understand my own adrenal gland. How amazing to test my courage every day. Brave people face fear, and I have the opportunity to stare it down every day. I may not always win, but I am never defeated.

I push myself to learn to weld, build, swim with sharks, jump from heights, climb cliffs, live in new places, hike to extraordinary places, and give my first kiss to my significant other. The pay off and the freedom is more significant to me when I know I can face the next challenge if I have something amazing that I've already conquered. I may not be the fastest or the most skilled, but I am not ruled by regret. No one should be. I hope your "disability" leads you to mountain tops and wave curls. You have my faith.

1 reply
User Profile: AutumnLeigh
AutumnLeigh April 4th, 2017

@Xotamato

You are an inspiration! Well said! laugh

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