Going Indie! Join me!

Some of you may know this. Most of you don’t.

I have been quietly working on a major transition for Radiant Abilities. Later this fall, I will begin launching a series of personal and professional development videos. The videos will be targeted to three separate audiences:

People with disabilities
Family members of people with disabilities
Professionals in the disability field

The videos will offer tools, strategies, and inspiration for people to step more into their power, embrace their disability, and feel empowered to go out and live the life they want, pursuing dreams and even taking risks.

Speaking of taking risks…

I am beginning to believe that taking risks are just part of my DNA. This is a significant risk I am taking in my business. While I remain committed to the counseling clients I have, I am no longer taking referrals for new clients. I made this decision a few months ago so that I could have more time to devote to the video development and launch.

The risk I am taking is believing this is the next step in a career that has been dedicated to helping people to not only cope with a disability, but live fully and happily with it.

The other big risk I am taking is a financial one. The videos will all be professionally produced, no videos loaded from my phone. Not that there’s anything wrong with that. I just wanted a polished look to the videos. I also now have a team of consultants who are helping me put this project together and letting people know about it.

With limited resources for this and my passion to get my message about living fully and happily with a disability, I am launching a crowd funding campaign to help raise the initial start up funds for this new business.

I am launching the Radiant Abilities – Living Fully with a Disability Campaign on Monday, September 15 on Indiegogo. People can join in at any dollar amount, although there are incentives for particular contributions. Here’s a sneak peek at the launch video for the Living Fully with a Disability Campaign:

http://vimeo.com/104422272

You’ll hear updates about the campaign in the weeks ahead. What I would love for you to do is share this video with just three people you know. I need many, many more people to know about me and what I am doing!

Thanks so much for reading and considering this project that is dear to my heart and soul.

Posted in LIVE your life, Radiant Abilities Video Series, Taking Risks, Video Posts | Tagged , , , , | Leave a comment

Radiantly Living Through Art

I was honored last week to speak at the opening reception for the 2014 Unique Art Exhibit. Unique is an annual magazine of visual and literary pieces by artists with disabilities. Unique is the creation of Arise, Inc, the independent living center in Syracuse, NY.

I have admired Unique since its inception in 2000 for the venue it creates for people with disabilities to bring forth their talents and gifts to the our community.

I was honored to be one of this year’s judges. What I was not prepared for, though, was being overwhelmed by the depth and range of the work.

I will never forget walking in the room where all the pieces are collected and stepping into a state of amazement by the breadth of the work.

The volume of moving visuals, along with the touching literary works, tells me we have a goldmine of artistic abilities in Central New York. Abilities that need to be given more opportunities to shine.

As a professional in the disability service field and as someone who has lived all my life with a disability, I see such a need to change our thinking from serving people with disabilities to helping them live fully by encouraging people to radiate their abilities.

Unique does this year after year.

Unique is so much more than art and fine prose. It’s about individuals reaching within and bringing forth strengths and abilities.

The very nature of doing so lends itself living life more deeply and with more meaning.

Some of these artists have produced their work from the painful process of living with a disability. This kind of alchemy is a reflection of living fully with a disability because the artists transform their struggles into gifts that are shared with the community.

When we do this, we tap into our abilities. Take a peek into Unique exhibit and for you locals, check out the exhibit in person at the Everson Museum through September 21.

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The Secret to Change

“The secret to change is to focus all of your energy, not on fighting the old, but building the new.” -Socrates

How true this is! If you’ve been there, done that, why keep going back?

I’m a firm believer in the power of change to help us grow and feel more fully alive and engaged in life. We sometimes need the messiness and challenge to our comfort zone to help us find renewed and usually more purposeful meaning to our lives.

Change often forces us to dig deeper into our well of abilities and discover new skills and talents within. Even when change is unwelcome, this powerful transformation can occur and we become stronger because of it.

The Socrates quote probably especially resonated with me right now because I’m in the midst of making significant changes within my business, Radiant Abilities, LLC. While I still provide individual counseling, it’s on a limited basis these days.

This is to allow me time to “focus on the new.” A primary piece of the new is a series of videos which will be released oMver the next year. The videos, geared toward personal development, empowerment, family support, and professional development, will serve three separate audiences – people with disabilities, their family members, and professionals within the disability field.

The upcoming changes at Radiant Abilities highlighted in the July issue of Syracuse Woman Magazine. You can check out the article, featuring me as the WISE Business Center Entrepreneur.

I am so excited to begin compiling my twenty plus years of professional experience – and of course, my lifetime of living with a disability – into downloadable videos from my website. These videos are intended to help people problem solve and strategize their way to living more fully with a disability.

Topics will include Advocacy from Within, Healthy Sexuality and Relationships (professional version as well), Releasing the Myth of Disability (professional version as well), Empowering Your Child with a Healthy Sense of Self, Defining Oneself, and Taking Risks, to just name a few.

As current subscribers to Radiant Abilities, you’ll be offered a first look at the videos and a gratitude-filled, deep discount on the longer videos.

Know someone who would benefit from all this? Please be to share this post and encourage them to sign up! They’ll get a discount off of Firewalk: Embracing Different Abilities.

Don’t have your own copy yet or need another one? Contact me directly and I’ll give you an even bigger discount.

I’d love to hear your ideas and requests for training or personal development topics for the video, so leave a comment below.

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Are We Really Inspiring?

Or are we just living lives?

That is the question posed and challenged to you in a video that ended up in my inbox last week. The answer is articulated beautifully by comedian and disability activist, Stella Young in a recent TED talk. This nine minute talk may challenge the way you look at people with disabilities and this whole notion about whether we’re inspiring or not. And that is a very good thing!

Stella captured what I have been thinking about for years now. Are people with disabilities viewed as typically inspiring for simply living pretty ordinary lives? Is it somehow inspiring when we grocery shop, pay bills, or go to work? If so, why?

“Because we have been told a lie about disability,” Stella says. “The lie is that disability is a bad thing and to live with one is exceptional.”

I love that statement. It so ties into I give on Releasing the Myth of Disability, which essentially teaches people to develop an awareness of the false societal belief that disability is a horrible fate. Stella claims (rightly so) that many people have a tendency to look at people with disabilities and think, “No matter how bad it is for me, it could be worse.”

There is so much teaching to be done to flip this attitude around and let society know there is joy and peace in living with a disability. Sometimes this serenity comes from the very fact we are different, that we don’t easily “fit in,” and we’re just fine with that. There’s also a lot of education needed about how people with disabilities often just lead ordinary lives and there’s nothing exceptional about that.

As I had the idea for this post rolling around in my head and was taking my evening walk with my son, who is still in a stroller, a man stopped along the trail to say to me, “I see you walking him (my son) here quite a bit and I got to tell you how inspiring you are.”

I thanked the man. I was not necessarily offended because I could tell the compliment was from the heart. He even touched his heart as he spoke to me. My belief is that if I can touch people’s hearts, then that’s the doorway to changing beliefs and attitudes.

After I thanked the man, I said, “Well, I have to get my exercise in somehow.” What I thought was how I was just doing a very ordinary thing – exercise – because heart disease does not discriminate against disability….and that I love this life of mine with a disability and want to keep living it for another 45 years!

Enjoy Stella’s talk, I’m not your inspiration, thank you very much; it’s so worth the nine minutes. Take her up on the challenge to question what you think you know about disability.

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Why Maya Angelou’s Work and Life Speaks Volumes to People with Disabilities

Last Wednesday, I listened to a news segment about the life and death of literary genius and civil rights activist Maya Angelou with tears rolling down my cheeks. I was not surprised by this, despite her books still being on my “To Read” list. I have been familiar with her work for years, though, and she always caught my attention in the media and of course, at Presidential Inaugurations.

Maya always struck me as a woman that radiated beauty and grace. I strive to be like her. It was not until Wednesday, the day of her death, that I realized why she had always struck such a cord with me. Maya’s life story of rising above the abuse, trauma, and pain of her past speaks volumes to beautiful process of finding one’s own sense of empowerment and ability to tap into one’s gifts.

Despite all the abuse and instability in her childhood, she stayed true to herself and believed in herself, perhaps when no one else but her beloved brother did. She then took that belief in herself and her gifts and rose to greatness.

Maua’s story inspires us all to find the greatness within ourselves, despite how daunting it may seem at times. Living with a disability is about acknowledging the challenge, the hardship, and then saying to oneself, “How can I rise above this?”

In these moments, you may also want to check out Maya’s poem that embodies empowerment, And Still I Rise. The entire poem resonates with me as someone who has struggled at times against being judged and excluded for my disability. Here’s the two excerpts that speaks the most to me about rising above the challenges of a disability:

You may shoot me with your words,
You may cut me with your eyes,
You may kill me with your hatefulness,
But still, like air, I’ll rise.

And….

Out of the huts of history’s shame
I rise
Up from a past that’s rooted in pain
I rise
I’m a black ocean, leaping and wide,
Welling and swelling I bear in the tide.

Leaving behind nights of terror and fear
I rise
Into a daybreak that’s wondrously clear
I rise
Bringing the gifts that my ancestors gave,
I am the dream and the hope of the slave.
I rise
I rise
I rise.

May YOU rise and shine as gallantly as Maya.

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The Best Dating Advice

Don’t give him your number, he needs to have the “full effect” of you.

I was visiting a friend, describing my latest attempt to try the whole online dating thing, when she gave me this counterintuitive, wise advice. I had just been explaining to her my concern that many men would unfortunately hear my voice on the phone, which is accented by my cerebral palsy, form a judgment about it, and I would probably not hear from them again. Often times, this is the harsh reality in dating with an obvious disability.

I have come to learn through this quote, life (and dating) somehow get easier once we accept the difficulty of it all:

Life is difficult. This is a great truth, one of the greatest truths because once we truly see this truth, we transcend it. Once we know that life is difficult – once we truly understand and accept it – then life is no longer difficult. Because once it is accepted, the fact that life is difficult no longer matters.
- M. Scott Peck

So I began to accept and embrace the fact that dating can be really hard and full of rejection. Please keep in mind this is true of people with ALL abilities. Once I did this, I could then problem solve.

I knew exactly what my friend meant by having a guy meet me and getting the full effect of me. He had to see how comfortable I was in my own body and with my disability. My friends often said when they initially met me, that’s what drew them to me – the ease I had in a body that was so different.

I was banking on that being true in the dating world as well. Since I was doing online dating, when a guy emailed and asked me for my number, I would write back and offer to meet him (at a public place, of course) and say something to the effect of meeting me would give them a much better idea of who I was. This would also happen only after several email exchanges, so I could have an idea about them.

My testing of this little Do Not Call experiment did not get far. The first guy who agreed to meeting me before talking to me was a lovely man, but I didn’t feel any spark there. The second, who I met a week later, ignited a spark the moment I walked into the room. That was the beginning of the end of dating experiments. We married two years later.

If you have a disability and are concerned that someone just talking to you on the phone will form a judgment about you without allowing themselves the honor of getting to know you, take a risk. If you want meet them, have them get the full of you. It may pay off big!

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Dating 101? No just some tips!

I want sex.

Knew that would grab you.

I have heard that statement in one way or another from almost ALL of my clients in my nearly 20 years of counseling.

Sure, who doesn’t want it?  Well, maybe  someone who’s eight months pregnant may not care for it. But then there’s the rest of us.

Do I really have to say that people with disabilities are no exception to this?? Yes, they clearly want sex and a lot of it, please. Remember, I work with many men. However, what people want more than that is to DATE!

Many of the people I work with are lonely. They want friendship and companionship. They want to get to know people. They” want people to get to know them. They want to date.

Sometimes people with disabilities (and I’m sure a good share of those without disabilities!)  need some guidance in practice and process of dating. I have a gentleman I am currently working with who has been asking me for conversation topics once he makes an initial connection with the women he “meets” through online dating sites.  Since his brain injury, it’s been harder for him to initiate social conversations. It’s also been challenging for him to think about all the steps involved in getting to know someone as a potential girlfriend. So I created this Questions for dating for him. I hope you or the people you work with also find it a helpful resource!

His request for guidance, along with my desire to make this blog and my website more resourceful, inspired me to create a new category for DATING RESOURCES.  In the months to come,  I will be adding more downloadable PDFs to this category ranging from dating safety tips to sexuality issues to knowing the right person for you.

I would love to hear your comments, questions, or situations you’re dealing with in supporting people in their quest to date and develop relationships in the comment area below.

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Define Thyself and Open to the Possibilities

In the past month, I have been introduced to Success magazine, a very motivating publication for being a leader not only in the business world, but also in your personal life. As I was finishing the current issue, I came across a wonderful quote by Jason Silva, filmmaker, that also applied to what I am doing with my business.

“[The whole point of my work is] to infect people with a sense of boundless possibility.”

That’s what I want to do, I thought. Since I published Firewalk: Embracing Different Abilities, I have been shifting my focus from the one-to-one counseling I have done for years to speaking to a more general audience about disability related topics, specifically focused on empowerment and living life more fully. What I have discovered is that my individual work with people has prepared me well for sharing tips and strategies with larger groups of people.

Much of the counseling I have done with people is how to help them “adjust” to having a disability. Given I counsel primarily people who have acquired a Traumatic Brain Injury, this makes sense. The word adjust is a clinical term. I am supposed to help people adjust to their functional limitations, apply coping skills, and develop compensatory strategies to adapt to the loss of functional skills (more clinical terms, you still with me?)

In my nearly 20 years of counseling, I have observed time and time again one of the core reasons why people have difficulty adjusting to a disability is that they allowed themselves to be defined by others’ definition of who they are because of their disability, rather than defining themselves. This is true of people both born with a disability and people who acquire one along the way. Often people just define themselves by how they think others perceive them. What an exhausting way to go because you’re investing so much mental energy in what you think others think!

I always say people are forever going to think just what they want and there’s no way we can control that. What we do have a lot of control over is how we define ourselves. Here are three easy steps for doing that:

1. Check in with yourself frequently. Ask yourself whether what your feeling or thinking about yourself belongs to you or someone else. If it’s the former and it’s a negative belief, see what you can do to reframe it. If it’s the latter, dismiss it. You have your own thoughts to keep you busy, you don’t need another’s.
2. Identify three positive traits about yourself and hold onto them like gold. For me these words are compassionate, energetic, and outgoing. Say your words like a mantra, let them radiate through you so they become a solid foundation of your self definition.
3. Develop a “definition filter.” If you do step 1 and check in with yourself about something you’re thinking or feeling and it does not match your list from step 2 (or just does not feel right for what you know to be true to you), filter it out!p Remind yourself that belief belongs to someone else and not you. Therefore, it has no bearing on who you are ultimately.

Once we begin operating from our own definition of ourselves, it’s amazing how much energy and capacity we then have to see all the possibilities open up for us on what we can do with our lives. This is because by defining ourselves, we are now steering the ship.

I haven’t gotten too many comments lately. If you feel so moved, leave one below.

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Why the Gayest Year Can Help People with Disabilities

This issue has been rolling around in my head for sometime now. I have been watching and listening to the news reports, legal decisions, and most importantly, people’s views and attitudes toward gay rights. It’s definitely changing. Gay marriage and domestic partnership are being both recognized and legalized in more states. Children are more easily adopted by same sex couples. It seems like the views that prohibited these rights for gays are either weakening or hopefully, reflect an understanding more of the importance of accepting people just as they are.

In December I heard a wonderful end-of-the-year summary of 2013′s progress on the changing attitudes of gay rights. National Public Radio’s Ari Shapiro summarized the legislative and attitudinal changes sweeping through the country in the last year. From state legislatures to Congress and even to the Supreme Court, same sex rights are being recognized and finally acknowledged as basic, deserving rights.

This reflects a growing societal acceptance of gay people. One that is so long overdue. How could one of the most developed countries, as we are, ever have a hard time embracing love between two people? I, as you may have guessed, come from the school of thought, that believes being gay is an inherent part of one’s self. After all, can you explain why you’re heterosexual or homosexual? I can’t; I just know I am heterosexual.

I was in a meeting last spring discussing the challenges that people with disabilities continue to face in regards to trying to help the general public become increasingly more accepting and embracing of people with various abilities. I mentioned that I thought that we could learn a great deal from the LBGT community and the gay rights movement. I believe the key of their growing societal and legislative progress has to do, at the very core, with self-acceptance and really claiming, “This is who I am.”

In the NPR piece the reporter captures this sentiment by quoting Harvey Milk. Milk was the first openly gay person to be elected to office in California. He is recognized as an early leader of the gay rights movement, perhaps because of this philosophy:

The most important thing gay people can do is come out because once you know us, you don’t hate us.

I believe the same principle is so very true for people with disabilities. While many disabilities force us to “come out” because they are so evident, claiming one’s disability as an integral part of who one is and having a sense of pride (think Gay Pride) can go a long way in people getting to know us and seeing our value.

Throughout my life one of the most common pieces of feedback I receive from people about my disability is because I am so comfortable with it being part of who I am, that allows others to feel the same. Like gay people, once we stop resisting such an integral part of who we are and what makes us different, we can proudly claim how we don’t fit into that elusive “norm,” giving others the encouragement to accept and embrace us as we are.

There’s a lot to learn here. Keep watching the gay rights movement. Maybe some year we’ll have the Most Differently Abled Year.

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Don’t Fall….Gee, Thanks for the Reminder

I have had a particular idea for a blog rolling around my head for a while now.  It needs a bit research and time for me to put my thoughts down. My family and I are in the midst of moving this week, so unfortunately time is a hot commodity.

Thankfully, the Universe delivered some good, lighthearted material for a post the other day. The theme of this “lighthearted” substance may sound like an oxymoron – projected anxiety. You know when someone sees you and begins assigning a worry or a fear they have onto you. I have found this happens from time to time when someone makes instant assumptions about because of how I walk.

In their eyes, I appear unsteady due to my gait and that causes immediate concern in the other person.  In general, I believe people have a difficult time being with their concern and even a harder time labeling it anxiety. If people were able to do this more, they would in a better position to catch themselves and project far less anxiety onto others.

Here’s my brief encounter to illustrate my point. Over the weekend, I got a haircut at a salon I’ve been going to for years. The salon¹s in an old house so there¹s a couple steps leading to the front door.  As I’m paying my hairdresser (do they still call them that?), her next customer comes it. I say goodbye and walk to the door.

As I do, the Next Customer follows me. My hairdresser, who has a knack for totally getting people for wherever they are, says to Next Customer, “Did  you forget something?” Next Customer replies, “No, I am going to help her with the door.”

Yes, a nice gesture, but I didn¹t really the help, nor did I ask for it. Plus, her holding the door made my exit a bit more challenging because I was not able to hold onto the door as I stepped down. It just threw off what is easy for me.

Then as I am descending the steps, Next Customer calls after me, “Don’t fall.”

I know it probably doesn’t  sound like this after  reading this post, but I¹m actually not a sarcastic person by nature. I’m not as quick with comebacks as I¹d like to be. What I would have loved to say is, “Thanks for the reminder. Otherwise I would have planted my face on the cement.”

Don’t fall. Like I’m trying to? Do people think before uttering these words?  No need to answer that one. Obviously not.  I¹m usually pretty tolerant of other people¹s comments, especially when I know the person is trying to be but has their own anxiety thrown in the mix.

Statements like “Don’t fall,” especially when the person knows nothing about me except that I have a disability is just condescending.  Would that woman have said the same to someone without a disability? I don¹t think so.

I will end my rant with a plea for all people who feel uncomfortable with anyone¹s difference, check in with yourself first – is what you¹re about to say coming from a valid place or one of projected anxiety? If it’s the latter, take a deep breath, count to 10, and people see themselves to the door.

 

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