Hate Crimes, Bomb Threats and Anxiety: Tools to Proactively Protect People With Disabilities

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Recently there has been a significant increase in hate crimes and bomb threats across the entire country. Minorities, including people with disabilities, are especially at risk not only for attacks and threats, but also for the stress and anxiety that can result from seeing what is happening around us. People with multiple minority status (i.e. people of color + disability, LBGTQ + disability, Jewish or Muslim + disability, immigrant + disability) are particularly vulnerable.

The one-in-five people in America who have a disability need proactive and systematic planning in order to ensure they have the same safety and security as everyone else.
Key issues and steps include:

Anxiety, Addiction and Emotional Health: Even for people who do not have ongoing mental health issues and who are nowhere near bomb threats or hate crimes, the content of social and other media can be extremely frightening. Emotional reactions can include feeling physically and mentally drained, having difficulty making decisions or staying focused on topics, becoming easily frustrated on a more frequent basis, arguing more with family and friends, feeling tired, sad, numb, lonely or worried, and experiencing changes in appetite or sleep patterns.

Most of these reactions are temporary and will go away over time. It is important to try to accept whatever reactions you may have and to look for ways to take one step at a time and focus on taking care of your needs and those of your family. Keep a particularly close eye on children and people with addiction issues (including Internet addiction) who may need extra supports.

Some things that can significantly help your mental health are to limit your exposure to the sights and sounds of stress, especially on television, the radio, newspapers and social media, as well as eat healthy, get ample sleep and stay personally connected to family and friends. Stay positive. Remind yourself of how you’ve successfully gotten through difficult times in the past. Reach out when you need support and help others when they need it.

Most major cities have a Jewish social services agency, which will help people of all faiths. Additionally, the Red Cross’ Disaster Distress Helpline is free and 24/7 for counseling or support. You can call 1-800-985-5990, text “TalkWithUs’ to 66746 or utilize Red Cross Mental Health Teams.

Another resource is the American Counseling Association. They have fact sheets you can download on mental health services, including post traumatic-stress disorder and crisis counseling. Moreover, if you are feeling suicidal, you should reach out immediately to www.suicide.org.

Create Your Evacuation Plan and Support System: Have you been in touch with your local
police station and fire department? If not, do it now. A part of the services they provide is to keep track of the needs of residents with disabilities in times of threat or disaster. For example, if you use a wheelchair and live or work in a high-rise building, the fire department should and will literally come out for free to meet with you and create an individual plan for you in case of a fire or other emergency.

If you have sensory, cognitive or other issues, it is vital for the police and fire department to know how to successfully support you in a time of crisis. Hundreds of Americans with disabilities are killed by police each year because the police have not been trained to recognize and address mental health or other disability issues. The time to have those conversations and training is before a disaster strikes. Because this issue is so important, RespectAbility has conducted a free webinar, which you can find on our website: Special Conversation With Special Olympics About Violence, Police Training and People With Disabilities.

When it comes to evacuating people with disabilities, you must plan in advance. See the National Fire Protection Association’s terrific Emergency Evacuation Planning for People with Disabilities (June 2016).

Have a “To Go” Kit Ready: If your building is evacuated, you will want to have several things handy. For example, you will want to have any medications you may need to take as well as your phone and charger, glasses, hearing aids and extra batteries if you use them, supplies for a service animal you may have and more. You also will want to let your loved ones, who might worry if they see a threat on the news, know you are OK. You can do that through phone, email or social media. There are terrific resources available through FEMA.

If you use a communication device, mobility aid or service animal, what will you do if these are not available? If you require life-sustaining equipment or treatment such as a dialysis machine, find out the location and availability of more than one facility. For every aspect of your daily routine, plan an alternative procedure. Make a plan and write it down and print it out. Keep a copy of your plan in your emergency supply kits and a list of important information and contacts in your wallet.

Create a Personal Support Network: If you anticipate needing assistance, make a list of family, friends and others who will be part of your plan. Talk to these people now and ask them to be part of your support network. Share each aspect of your crisis/emergency plan with everyone in your group, including a friend or relative in another area who would not be impacted by the same emergency and can help if necessary.

If you have a cognitive, intellectual disability, or are deaf or blind, be sure to work with your employer and other key contacts to determine how to best notify you of an emergency and what instruction methods are easiest for you to follow. Always participate in exercises, trainings and emergency drills offered by your employer or landlord.

Our nation is at its best when we are welcoming, respectful and inclusive of all. As many people are, or feel, at risk, we must show exceptional love and friendship to those around us.

Special thanks to Elliot Harkavy for ideas and contacts that contributed to this piece. 

Learn more at RespectAbility.

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Why Play Dates Require Planning as a Mom With a Disability

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My daughter is 5 and has quite the social life! She’s made many friends from various facets of her life and my life combined – school, church, sports and recovery meetings. She’s the type of child who writes an invite list to her birthday party that’s longer than her Christmas wish list. Needless to say, she is asked to join friends for play dates on a pretty regular basis.

This is where Mommy becomes more of a detective than a parent. This is when I bust out with my list of questions for the parent whose house I’ve never been to. I have to consider everything about the structure of their home and its accessibility to me before I can decide if we’re able to go or not. Are there stairs leading into their home? If so, are there hand rails? Is the house all on one level? Are there carpets? Rugs? Toys or clutter of any kind in the middle of the floors that I’d need to try to navigate around? Is there an animal who might jump on me, causing me to lose balance? Or could the animal be so small and fidgety that I trip over them or can’t process all their movements in order to walk around? What’s the bathroom like? Is there something I can hold onto while in the restroom?

If you think this list of questions is long, think of how I feel asking all of them. For starters, I never truly trust the answers I’m given. I may trust the person completely in every other way, but able-bodied people do not have to think like I do. I myself never thought this way until I became disabled, so I surely can’t expect others around me to understand my needs immediately. I get nervous that something’s being left out: a small step up into the foyer; those two tiny stairs up the sidewalk that the person forgot to mention, and oh, there’s no railing there either; the fact that the bathroom is on the second floor.

I become concerned my daughter will be so excited the day of her play date, yet when we arrive at her friend’s house, there will be some barrier preventing me from entering the home and we’ll have to either move to our house (which is way less exciting because other kids’ toys are always the most fun to play with!) or reschedule for another time and decide where to meet that’s accessible for me. And, there have been those instances where we’ve not made it into the house, even though I asked the litany of questions.

I feel guilty and can’t even pinpoint why – some of it is because I wish we could just go like other families do. I wish I could be a “normal” mom for my little girl. I have guilt when we must meet at our house, knowing my daughter enjoys playing with toys that aren’t hers. Yes, kids often bring toys from home to share, but it would be nice if my child could get out of our home more.

I feel like I’m interrogating the other parent; as if I’m making sure they have the “right” kind of home. I worry they’ll be insulted by all my questions – here they are, treating me like any other mother (as I deserve to be) but I’m asking them tons of structural questions and focusing on my differences. I feel like it may seem I’m making a big deal out of a simple play date. “Wanna come over and play?” For most families it’s a “yes” or “no” question, not an opportunity to ask for the blueprints of the person’s house. But it’s what I must do in order to know what my answer will be.

There’s a small part of me inside that whispers quietly, “This is OK. Don’t feel guilty. Don’t stress out. God didn’t make a mistake in making you, nor making you a mom.” That wee small part of me also insists that it’s just a play date. The important part isn’t where the playing occurs but how (with enjoyment and happiness), why (because my daughter is a wonderful, funny, compassionate friend) and that it is happening. When she’s 20, I’ll ask her if she remembers having play dates with friends – I bet her answer will be along the lines of “Oh, yes! I had lots!” instead of “Yeah, but they were always at my house.” She’s got the best attitude about everything… even though her mom’s attitude can be saturated with worry, anxiety and guilt. Guess that’s just another thing that proves I’m like any other mama!

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To the Man Who Doesn't Believe I Need a Service Dog

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Two years ago I was diagnosed with PTSD, agoraphobia, bipolar disorder, and major depressive disorder. This year I have been diagnosed with POTS, postural orthostatic tachycardia syndrome. My family and I decided that one of the best options for my treatment was a service dog to help me with my panic attacks, my night terrors, and to give me emotional comfort when out in society. Being 14 about to turn 15, I was not in favor of having a Labrador retriever or something similar in size because I didn’t want that kind of attention. So we agreed a Chihuahua would work best for me.

We trained her for a year and a half, and she has since been simply perfect at her job. We have started training once again so she can learn to work with a wheelchair, as I now need one because of my POTS. I understand that because she is so tiny, at first it might be hard to believe she is in fact a service dog. But if you casually watch us going about our daily lives, you can see and judge by her behavior and not her size.

I am assuming (but I’m not sure) that you, sir, did not watch us for even a second before you so rudely told me I looked healthy and there is no reason for me to be dragging along my “service puppy” — your words, not mine. I told you that she was not bothering anyone, and she has every right to be by my side in the store. Before you could say anything else, I turned and walked away. You, sir, have absolutely no right to make that assumption about me.

You have not seen me at my worst, when I wake up in the middle of the night gasping for air because just a second ago I was convinced I was being attacked all over again. You did not see me when I stood up from the bathroom floor, only to fall unconscious again and have no way to call for help because I couldn’t get up and risk fainting again. You are not there for me on the days I can’t even lift my head from my pillow because it would cause me immense nausea — but she is. She brings me a bottle of water to swallow my anti-nausea pills when I can’t get out of bed. She comforts me in the middle of the night when I can’t breathe from the terror of the nightmares. She fetches my cell phone for me so I can call for help without risking my life.

Please, I ask you to keep your thoughts to yourself about all of these “unnecessary service puppies.” These dogs are in fact very helpful to a lot of us with chronic illness or disabilities. You do not see my struggles. Just because you can’t see my disabilities when I’m at the store, it doesn’t mean they’re not there.

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Laura Robb, young woman in a blue power wheelchair sitting outdoors near a lake..

What I Want to Show the World About Life With a Disability

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Before I wrote this post on 10 common misconceptions about people with disabilities, I reached out to people online who also have various kinds of disabilities. I soon realized — we are all clashing with culture in similar ways. We face the same assumptions attached to our visible limits.

I wish I could tell you I don’t hear the following questions very often. But I heard question #1 and #5 about me just a couple of weeks ago when I was out with a friend.

1. How old is she?

2. What’s her name?

3. Can I pray for her?

4. What’s wrong with you?

5. Are you her _______ (fill in the blank with a family member)?

The questions themselves aren’t necessarily the problem. It’s the way the person approaches the conversation. So many times they don’t acknowledge me. They don’t start with a “Hello” or “How are you today?” Nope. They jump right into asking me (or the person with me) one of the five questions.

I sit in my wheelchair, sometimes shocked into silence, sometimes annoyed and hoping to hurry up the interaction. I’m still surprised when I see misconceptions in action. I’m trying to learn — how can I teach this person on the spot? What can I do to spread a little awareness right now?

I admit I’m not always ready to answer in depth. Putting words to what happened and understanding why I grew frustrated prepares me for the next time. Because sadly, there will be a next time.

We long to fight what is being assumed and show the world —

Our lives are not less than.
Our bodies are not less beautiful.
Our stories are not less exciting.

We, the people living with a visible limit, want to remind you —

It’s not about what you see on the outside.
It’s not about what you assume is a limitation.
It’s about looking beyond all that.

We simply hope you will find the me behind the disability.
Those who see beyond the visible are the ones we want in our lives. They are the people who matter to us.

Listen to culture less.

Love the ones who care more.

Then, we can worry less about bridging the gap… because we’re already building a stronger community for you and me.

Changing these misconceptions begins right outside our door.

Are you in?

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Brooklyn Public Library Mails Books to People With Disabilities

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The Brooklyn Public Library offers a Books by Mail service which mails library assets to people with disabilities.

Read the full transcript:

This library mails books to people with disabilities.

Brooklyn library’s Books For Mail program delivers library books to your doorstep.

The service is provided free of charge to those with physical disabilities or visual impairments that can make it difficult to go to the library.

The library provides a wide selection of regular print books, large print books, books on tape and videos.

Similar programs are also offered by other New York City libraries such as Queens Library and the New York Public Library.

To learn more, visit bklynlibrary.org/seniors.

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Dear 16-Year-Old Me: Your Diagnoses Will Not Define You

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In the next seven years, lots will happen… keep your cool. You can do this.

1. You feel old at 16. You really aren’t old. You’re still a baby really.

2. You can put makeup on if you wish. If any of your “boyfriends” (I use this term loosely) wants you to wear makeup, what is this saying? Don’t do it to please him, I beg of you. If you want to wear makeup, do it. If you don’t, don’t. Also, the makeup phase you went through… you either look like a ghost or an orange, so make sure you get some advice from the drug store assistant in selecting the right shade. Please, respect your skin.

3. Don’t jump into a relationship so quickly. Boys are cool… I get that, but don’t make the mistake of being someone who is just there when he wants you to be…don’t let him use you. Your broken heart will mend. After your relationship ended, you felt heartbroken for a while. Accept the good times that were had and move on… but take heed of point number two.

4. Don’t miss out on family time for the sake of fake relationships and friendships. You only get one family… love them while you can. Your parents love you more than you realize.

5. It’s only at the age of 23 that you’ll begin to realize the importance of self-care — especially when it comes to trying to gain some control over your chronic illnesses and emotions.

6. Your chronic pain will still be with you at age 23… but don’t be sad about it. As a 23-year-old, pain is literally a part of my life as it is of yours at age 16. There’s no point in me lying. You’ll have some horrible times with it that require urgent medical care, but you’ll also have a select few times in which you are as pain-free as you’ll ever get to. You’ll also discover that friends close to you also have your condition or something similar, and they will understand.

7. You’ll still need surgery.

8. Don’t over-exert yourself. I refer back to the point of self-care.

9. The bags under your eyes will remain… sorry. This can’t be helped; blame the medication.

10. You’ll still be in your wheelchair. This is something I know you hoped wouldn’t happen, but it has, so just accept it. At age 22, you’ll get a brand new, beautiful wheelchair that you’ll fall in utter love with. A beautiful black wheelchair with sparkly purple bits (your favorite color!). Look forward to that. It’s amazing.

11. You’ll drive. Those people who said you wouldn’t be able to drive were wrong. Hand controls do exist! You’ll go through two cars and absolutely love both of them. Your hand controls are also pretty funky, and people will also want to know how you drive — show them.

12. You’ll make some amazing friends and rekindle old friendships. You know those friends you thought you wouldn’t chat with again because they’re too busy getting on with their own lives too? Well, you’re wrong. They’ll soon become the greatest of friends to you and you of them. You’ll never know such love for friends as you do with them.

13. Please don’t give up on your sporting opportunities. You’ll sincerely regret this as an adult. Even though you’ll eventually go back to wheelchair basketball, if you had stuck if through then, you could have traveled the world and made your career out of it.

The author at a party smiling, wearing black top with silver glitter

14. Be honest. You’ve always been honest but as an adult, this is of even more importance.

15. Stop worrying about other people while forgetting about yourself. That friend who just decided to up and leave? That wasn’t your fault… it can be a part of growing up.

16. You’ll experience some absolutely terrible and life-changing situations you would never have imagined possible. Your viewpoint of life and the people around you will evidently change, and your life won’t ever be the same again. You’ll fall into a horribly dark place, but you’ll be lifted out. You’ll grow up and mature as a result of it. Don’t worry… you’ll get through it. Take all the help you get; don’t be stubborn.

17. Your cancer, your wheelchair, your anxiety and your chronic illnesses will not define you — they are just an additional part of you.

18. Your morals, values, wants and needs will change. Accept it… don’t challenge it.

19. Your wheelchair basketball club will become like your second home. Value the people in it, because they’re amazing.

20. You’ll have two jobs, and oh, did I mention you’ll go to university? You won’t move out, but you’ll be at university! Three years of university will go very fast. (I didn’t believe anyone who said that either.)

21. Did I also mention that you’d be set to becoming a teacher in September 2017, but for a number of different reasons, it didn’t happen this year? Don’t worry. Your friends and family will always support you and actually, after discussing it in some depth, you’ll realize you made the right decision.

22. Be open with the health professionals. Whatever you say is nothing they’ve not heard before. Leave your dignity at the door.

23. Trust yourself and your instincts. You are right — trust me.

24. Don’t let certain people control you. You are your own person.

25. Scared of doing something? Take that leap of faith.

These are only some of the things that will happen, but take each day as it comes and don’t expect too much from yourself. You’re doing great at this “adulting” business (even if I do say so myself).

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