Invisible Disabilities Association

I have been a long-time supporter of both Habitat for Humanity and the Alzheimer's association--2 fantastic organizations serving to bring relief to different segments of society. But IDA is an amazing organization attempting to help folks who suffer similarly but are in fact "invisible" to most of the rest of society. I strongly support IDA, its mission and Wayne Connel its founder and leader. Please give today!

Through the Invisible Disabilities Association, I have learned a lot about how different Invisible disabilities affect people and how I can make small changes in my life to help those around me.

This organization has helped me become more compassionate and caring for people with invisible disabilities.

IDA has been a wonderful organization to represent as an ambassador. In 2021, I was navigating mounting diagnosis and symptomology and soon discovered IDA, online. I was inspired as I dove into the history and present impact of the organization and I wrote a song about my personal experiences with Invisible Disabilities and my family. Who knew that almost 4 years later, I would continue to walk alongside these amazing people and serve as a mouthpiece for impact in my day to day life.

The impact of the Invisible Disabilities Association is undeniable. Through years of watching the organization, I have seen just how many people it has reached and helped through some of life's most difficult challenges. As the organization continues to grow, I have no doubts that its amazing impact will, too. The Invisible Disabilities Association reminds all people that they are valuable no matter their circumstances or conditions. It is a message that I believe in wholeheartedly and is needed now more than ever.

IDA has had a profound impact on my life. Through the years I have learned to be more loving and sensitive to family, friends and strangers going through chronic pain and suffering. I have eliminated chemicals and toxic perfumes from my home and lifestyle. And I have been profoundly inspired by hundreds of people who suffer with an invisible disability and yet live amazing lives full of meaning and blessing to others. The people who help run this organization are very loving, committed individuals who have incredible integrity. I recommend this nonprofit.

The Invisible Disabilities Association has been an important part of my life as an Autistic Advocate. They are doing great work in assisting my advocacy but more importantly in the plethora of work they do with and for others.
The IDA has been working diligently regarding legislation for those with Invisble Disabilities not only in Colorado but other states as well.
www.invisibledisabilities.org

People with invisible disabilities face discrimination because there are many false assumptions about what someone with a disability should look like and act. Invisible Disabilities Association helps to educate folks about myths and misconceptions.

IDA is a great group that is on a mission to help the Invisible Disability community. As a person with CRPS, I'm really grateful to have found IDA. Everyone that I have "met" (virtually), has been really supportive and kind. Folks with an invisibility need organizations like IDA to help bring awareness of invisible Disablities, have a community, and to have support. Thanks IDA!!

Volunteering with the Invisible Disabilities Association (IDA) has been an incredible journey for me. This organization has truly given me a sense of purpose and fulfillment. The work they do has a positive impact around the world, and it's such an honor to be part of something so amazing. Being involved with IDA has enriched my life, and I'm so grateful for the opportunity to contribute to such meaningful work.

I have had an incredible experience with Ida. From their events to their advocacy. I was fortunate to attend the brain symposium, where I learned from some of the greatest medical minds. To their work with efforts to get invisible disability designations on state id's and drivers licenses.They are a mighty voice in this space.

My definition of a disability is any medical condition that impacts your life every day — seen or unseen. I have three invisible disabilities but if you look at me, you’d never know my life is significantly impacted by disability daily. That’s why The Invisible Disabilities Association is vital. They support those of us with these disabilities and educate everyone else about their magnitude.

Invisible Disabilities represents the best interests of so many of us who have disabilities no one else would know about just by looking at us. What a relief and gift this organization has been for me. I feel seen, heard and supported. Thank you to Wayne and Sherri for taking on this enormous contribution to our society, and for never giving up on us!

I am thrilled to share my experience working with the Invisible Disabilities Association, an organization that has an unwavering commitment to making a positive impact in our community. My sister and I were looking to get more involved in spreading awareness for people with invisible disabilities and their loved ones. We appreciated being able to connect with Jess and Wayne, who were very open to scheduling calls on how we can help out. Invisible Disabilities Association stands out for its transparent and impactful initiatives that address pressing social issues. They provided a presentation and opened up a conversation at our university on the experience and obstacles of living with an invisible disability. The students who attended the event were very grateful for this conversation and education, in addition to all of the resources and help they provided. The team's passion for creating meaningful change is evident in every project they undertake. Whether providing essential resources to those in need, promoting education and awareness, or fostering community development, the Invisible Disabilities Association goes above and beyond to make a difference.

Through my wife, Cathy Turner, I learned about IDA.
I’m in awe of all y’all have accomplished.
We follow your work because Cathy has an invisible disability.

My name is Katiya Xiong and I am the founder of DEEP Coalition, a global movement on empathy. I am more than happy to share my honest thoughts on Invisible Disabilities Association (IDA), an amazing nonprofit that was created to debunk myths around people living with disabilities. The impact that IDA does for individuals, families, businesses, and communities is no different than shedding light on the truths that should have been taught to us early on whether it be at home, school, or work. In the many years of my support of IDA's mission, I say with great pride and love that the organization's efforts are necessary to creating meaningful change for a better world. How is IDA special or why IDA? Because the organization has a vision of the future that will help those 'who are able' to better support, understand, and embrace those who are living with invisible disabilities: ADHD, bipolar disorder, schizophrenia, etc. My first introduction to IDA was about a decade ago when I had the pleasure of recruiting the nonprofit's founder, Wayne Connell, to speak at our annual summit; to this day, I can still remember some of the takeaway lines from our audience of 500, "I have always imagined disability to be a physical condition. It never occurred to me that maybe what my naked eyes are telling me can be so wrong. We need a better identification system than the wheelchair symbol to better represent all disabilities." As someone who continues to follow IDA's social activities from nearby and afar, I can attest to the need for this nonprofit's deep work and how important the ID Card programs and educational events are needed across cultures and regions. My final words are, "Choose IDA and everyone wins."

Having fibromyalgia & arthritis, the work and advocacy that Invisible Disabilities does is invaluable. They are a strong & needed voice for so many of us who have disabilities you cannot see.

Very well run organization. The staff is totally dedicated to helping with awareness and providing support to those with invisible disabilities. We have been supporting them at an increasing level for several years and will continue well into the future. It is clear that the Invisible Disabilities cause is personal for the staff and board.

I have been using the resources from this organization for over 10 years. They have great information on their site!! I've handed out their pamphlets and business cards to total strangers. I've recently been volunteering for their yearly online "gala" livestream and it's been so much fun!! Can't wait to see them grow into a large organization with more amenities!!

This organization has educated me about the thought process of understanding that not everyone's disability is visible. I had never thought about it until several years ago a very good friend, Carole Mitchell, spoke to me of her struggles with being around people who wore cologne. She explained how it affected her and made it difficult for her to be in crowds at times and what it did to her body. She told me about Invisible Disabilities Association and what they do. I was honored to help with some of their events and listen to so many wonderful speakers who make it easy to understand and want to help.

I have made it a point to become more aware of others and to provide the tools and information about this group to those who need it. This group makes a difference.

The Invisible Disabilities Association is an excellent resource for so many patients and their loved ones. It is a refuge and beacon for people who are in pain and despair.

As someone with a rare invisible muscle disability, I've been so glad to find and connect with the IDA. I've felt a wonderful sense of purpose and support in being part of their inaugural Walk and Roll fundraiser, hearing others' stories of their invisible disabilities, and becoming an ambassador for the work they do. Wayne and Sherri have the most amazing energy and put so much into the IDA, and it shows by how far-reaching the impact is across not just the US, but Canada (where I'm based) and elsewhere as well.

It is so difficult to have several invisible diagnosis. Most people see the out side of me and assume I am fine. So therefore I get very little support. Even my husband sees me pushing through my pain to give us a " normal life". But to have this community, Invisible Diseases if key to my coping with the daily hell of feeling so bad inside my body 24/7.

Really cares and brings awareness to an important topic!
OHIO has a proclamation for invisible disabilities week!

“I have been associated with the Invisible Disabilities Association for a few months now and I must say that the founders are doing an amazing job. The team's efforts to raise awareness about invisible disabilities and provide support to those affected by them are truly commendable. IDA's leadership is not only raising awareness and funds but also drives regulatory changes that help build more inclusive communities.

If it weren’t for this organization, I wouldn’t know that I had an invisible disability. They’ve been able to give me the words and resources I need to ask for accommodations and extend compassion to myself.

The Invisible Disabilities Association brings to light the needs of so many who have been in the shadows for decades. From my Great Uncle's battle with MS, my cousin's dyslexia, and my children's struggles with dyslexia and ADHD, my family has been effected for years. My wife and I, in our own personal search for understanding of ourselves, have identified our Autism Spectrum Disorder and begun to realize how it has molded our entire lives. All of these issues have been hidden from us for years, but the work of the Invisible Disabilities Association is helping to ensure that they are "Invisible no more." IDA's amazing work is empowering others to understand themselves and to be understood by the world. I'm excited to be a part of an organization that opens minds, hearts and eyes to the unseen needs of our community.

It was great, and very informative. Always a pleasure attending these seminars.

We highly recommend IDA. They are amazing and have such a great outreach and support

I will never forget how happy I was to meet Wayne Connell and listen to him share the IDA story of how the organizations helps instill a sense of belief and trust for those of us who manage invisible disabilities. When he asked me to come on board and volunteer, it was absolutely clear that this was a non-profit with which I must align. Their professionalism, compassion, track record and desire to bring visibility to those who aren't seen, heard, respected or understood is commendable and so needed. I am proud and honored to volunteer for IDA as their Director of Communication, and I look forward to sharing this crucial message with the world. THANK YOU, IDA!

I have followed IDA because of the effective efforts and challenging work done by this organization. The new awareness of what invisible disability means is a daily focus of Wayne Connell and Jess Stainbrook.
They have been successful in getting State level approval for adding a signifier to an individuals' drivers license to help those with i.d.a. get special attention when necessary.
I look forward to their guest speakers shared on many platforms; anyone can benefit from the webinars if they choose to follow IDA.
The annual gala to recognize others and how they, with their own invisible disability share in the quest to help us all understand the impact of seeing un.see.able disabilities in those we encounter daily. We are not here to judge but to serve.

The Invisible Disabilities Assocation serves as a source of inspiration, community and authenticity. As a person with multiple invisible disabilities, I have been impacted by their existence, in addition to the resources and opportunities to serve. As an ambassador, I get to operate as a modicum for outreach in the various roles I play as an advocate.

Having lived with multiple invisible and disabilities since I was born, I have felt alone my entire life because there really isn't anything out there that is truly representing us. When I stumbled upon the invisible disability association, I was thrilled to see the work they are doing. They are truly taking continuous action to make sure that our voices are heard, that we are invisible no more and giving us the access and the support that we need as we navigate this, journey.

This is an amazing non profit that brings awareness to this underrepresented sector of our society. It’s an honor to be part of the board because I also have the invisible disability that is registered with the state of Colorado and this has been an amazing forum for me to help share my story and help bring awareness to our community.

A great initiative with great founders who have fantastic hearts and the drive to bring invisible disabilities to the forefront. A worthy cause that everyone should be aware of.

It was my honor to meet and get to know Wayne Connell and be introduced to his nonprofit, Invisible Disabilities Association (IDA). Wayne and his wife Sherri have brought much needed awareness to physical and mental ailments experienced by millions of people around the globe. Each one of us have friends and/or loved ones who have to live their daily lives suffering, struggling, yet hoping for relief and possible remedies to their invisible illnesses. I'm happy to have learned about IDA and support their mission to help so many in need. I support the great cause of the Invisible Disabilities Association.

I wish Wayne and IDA the very best!

Gary Laney

We did a lot of looking around before selecting a philanthropy to be the official one for LockedBrands. We are a small tech startup and did not want to get lost in the crowd with all the big guys. And we wanted a philanthropy that was relevant to our Mission. The folks at IDA made it easy.

The IDA execs immediately saw the alignment of our Mission with a big part of the folks with invisible disabilities. In particular, the need to keep expensive and potentially dangerous meds safe and secure!

Wayne Connell and Jess Stainbrook were so easy to work with and were dedicated to getting us onboard. We gladly make a donation to IDA for every product sold. We are proud to be associated with such a great philanthropy and look forward to working with them for many years going forward.

I have the privilege of knowing and working with Wayne Connell and seeing first hand the amazing things this associate does. They are brining to light issues that people struggle with and help to bring support, awareness, and kindness to this often forgotten about community. As a former caretaker myself, I am very grateful to this associate for all they do to support this community.

As a senior leader in a Fortune 250 tech company, Invisible Disabilities Association has certainly impacted my ability to lead. The biggest impact has been in raising my awareness of many of the unseen challenges those I lead may struggle with each and every day. With the resources available from IDA I'm able to make more informed decisions that will not only benefit my team but also improve the effectiveness of our business.

I found out about IDA right before Invisible Disabilities Week this year. I've been living with an invisible disability all my life and only recently learned that this nonprofit exists. They are doing incredible things for the invisible disabilities community by advocating and raising awareness for folks like myself, and their #InvisibleDisabilitiesWeek campaign really made a difference on that front, bringing the existence of invisible disabilities to the forefront of our news feeds on social media. At their awards gala that night, I learned that they are working to establish an "invisible disabilities ID card" which would help folks with invisible disabilities to be recognized and potentially offered help when they are out and about wearing their ID tag. Their efforts to have these tags officially recognized is commendable and deserves all the support they can get!

Thank you, IDA!

IDA is an excellent advocacy group for those who have invisible disabilities. They give hope and a voice to people who are not often heard. I am so thankful that I have the opportunity to partner with such a great and passionate group of people.

Hard working, kind, professional, inspiring organization.

This organization is the epitome of empathy. Better yet, the founders speak from experience by shedding light on those who fight every day to be understood in light of their invisible disabilities. It’s an honor to work with the IDA team.

Few of us who are lucky enough to be ambulatory and lucid ever consider the issues associated with being disabled. The disabilities incurred by my wife from the negligence of others, that she must live with daily, are simply not in the line of sight of the people who observe her strength and benefit from her talents. To a trusted few, the story is told, and the pain and limits are understood. However, by and large, the world has no empathy for that which it cannot see.
When I heard of the Invisible Disabilities Association, I was pleased to hear that others were willing to give voice to the millions who persevere through unrecognized pain, or conditions that disrupt their lives. Invisible disabilities are unselective and affect us without regard to age, color or politics.
I advocate for the support of the work of Invisible Disabilities Association and urge all to take advantage of the upcoming event Love Ideas Summit on November 16-21.

I was made aware of the Invisible Disabilities Association almost five months ago by a friend who was working with them on the idea for the Summit that will take place November 16 - 21, 2020. More than 40 years ago I suffered a skull fracture compliments of a drunk driver; twenty-nine years ago I had a toxic injury that burned my lungs compliments of a negligent gas station at which I was covered head to toe in gasoline . I never before realized these injuries had a category - invisible disabilities. Disabilities that I suffered with in silence because few could readily observe or comprehend the magnitude of their impact on my life. Working with the leaders of the organization on the summit opened my eyes to the value of what they do; it also opened my eyes to the dedication of these people and this exceptional organization. I am proud to have made my small contribution to this upcoming summit and will continue to support the Invisible Disabilities Association in whatever way I can.

Let me tell you the real inside story about IDA founder Wayne Connell...He’s kinda crazy. He is a wild-eyed optimist. He is a workaholic. IDA helps hundreds-of-thousands of people, and for 20 years of its 24-year existence Wayne has run it completely on his own. Five days a week he works a full-time “real” job, and at night he puts in several hours on IDA. And he works on IDA over most weekends. And I don’t think he’s taken a vacation in 5 years. Okay, so here’s the goal: We all need to join together and figure out a way to get Wayne fired from his full-time job...so he can devote 100% of his time to helping the world. Here’s the plan: We need to join his army of volunteers and help raise a gazillion dollars for IDA so Wayne can do more of what he was born to do!


Greg Godek
Author of the #1 bestseller “1001 Ways to be Romantic”
Founder TheRomanceProject.com
Co-creator with Wayne of the Love Ideas Summit (LoveIdeas.org)

Invisible Disabilities Association is a stellar resource in the disability community that remains committed to supporting individuals living with invisible illnesses and their loved ones. As an employee of company that partners with IDA often, I've witnessed firsthand how IDA serves those who may need guidance on navigating an invisible disability, or just validation that what they're going through is real and that they're not alone. Thanks, IDA, for everything you do!

This organization recognizes a highly underserved, under appreciated population: those of us with invisible disabilities. I have been involved with them through the lens of a stage 4 colorectal cancer survivor. Not all patients in treatment lose their hair or lose weight, but yet go through brutal treatments that render us scarred, battered, and beaten down unseen to the naked eye. I am pleased to bring awareness to this issue through the good work of IDA.

I have been volunteering with this organization for a little while now and have seen nothing but genuine care and compassion from Wayne and Sherri. They are truly in this for people who have invisible disabilities or who are caregiving for someone who does. Their passion for helping those in need or those who just want to share their story and be included in a community is as plain as day, and anyone who has reached out to the Invisible Disabilities Association can see and feel that. It has truly been an honor and a pleasure to work with such a kind and dedicated team.

I am excited about IDA because they are committed to awareness, support and making a difference in so many peoples lives. As well as bringing value to audiences with their talented connections, leaders, speakers to help support those in need.

I am Gary Barg Founder and Editor in Chief of Todays caregiver magazine and caregiver.com and author of three books on family caregiving including" You Are Not Alone" regarding Covid-19 caregiving. I was pleased to be asked to take part in Invisible Disabilities Association's Love IDEAS Summit. This is an extremely important organization shining a light on a often overlooked issue for family caregivers and our love ones

I first saw Invisible Disabilities on Facebook. Since I contracted Lyme Disease, I have been hit with the words, "You don't look sick" repeatedly from family and friends. Maybe it was said to make me feel better, but I was already struggling to get a diagnosis so it just made things more confusing. I am not able to be as involved with IDA as I would like, soon I hope. I am proud to be part of a group that recognizes, gives assistance, support and provides a soft place to land for the people with invisible disabilities. Thank you again and again.

The Invisible Disabilities Association (IDA) provides tremendous awareness and support to individuals who have a disability that is not visibly apparent. outwardly the individual may look fine, which makes it hard for their family, friends, and the general public to understand what they experience. The support groups help individuals connect with other to share their experience and get helpful information. I am pleased that my organization supports IDA.

Numerous discussions with the leaders, attended their Gala 2 years in a row and while I was on the board of the Autism Society of America I worked with Invisible Disabilities to put our support for their effort to get an invisible disabilities marker on state driver licenses and ID cards. As an autistic person this is important as I may respond in a way that is different and would much prefer any law enforcement has an easy reference as to why instead of assuming bad intent.
From looking at what they have accomplished and they budget they have done it with they are probably the most efficient non-profit I have seen.

My experience with the organization has been amazing. Having dealt with the challenges that I face with Invisible disabilities its nice to have found an organization that understands and supports me.

Invisible Disabilities is a wonderful organization and charity who helps bring national awareness and helps make resources available to those like myself who suffer with invisible disabilities or a hidden disability. They have a community area on the site where people can interact with others who deal with the same illness as well as they try to connect with businesses and individuals in the country who share a similar mission. In my professional life, I have also interacted with the staff of IDA and they have always been a pleasure to work with and we are working to collaborate on various things and attend their Awards gala each year. I admire what they are doing because many people associate a disability as someone who is handicapped or 'in a wheelchair' and they are helping to bring awareness that disability is not always something you can 'see.'

What a God given joy to be able to share what you have with others WOW!
If you have ever been down and out and so sick that you could not even move without a helping hand - then you kinda know what I am talking about.
I believe this is what the Invisible Disability Association is all about.
Being able to help those who are not able to help themselves.
What an honor to be a helping hand. You can smile within itself.

I have been working with the disabled for nearly 13 years and any program that supports those I am all in. I currently am a certified work incentive coordinator and working with an employment network via the ticket to work program. I love this program!!! I see success being more than just an income, so much more.

Very dedicated and diverse group of persons committed to improving the lives of persons with Invisible Disabilities through advocacy, awareness and resources. Paula Vieillet- My Employment Options

I went to the 2018 annual gala as a guest of client that is very involved in volunteering for the organization. I had never heard of IDA, or really given any thought to invisible disabilities. I had an incredibly eye-opening evening as a learned of various invisible disabilities and what those that live with them go through on a day-to-day basis. I learned that family and friends that I care deeply about have some of these invisible disabilities and I'd never truly thought about the struggles that come with them. Fast forward to 2019 I was honored when Wayne Connell (founder, president, CEO) asked me to serve as one of the Young Professional Co-Chairs for the 2019 annual gala. I gladly accepted and helped garner attention for the event. I was so excited to have my family and friends attend in hopes that would feel the same impact I had the year prior. Undoubtedly they did and it was a wonderful event yet again. IDA does so much for so many people that live with invisible disabilities and it is truly inspiring how they bring people together from all over the world to bring attention to their cause and create communities of support.

I'm proud to support and donate to Invisible Disabilities Associations. I know my donations are going to great programs like the National ID Program that will help all people with invisible disabilities. IDA is great at bringing together many different disease groups to work together as allies and learn from each other.

I loved how IDA reached out to all with invisible disabilities and published any submissions of anyone who wanted to participate in Invisible Disabilities Week. It's so rare for the disabled community to get such a bright spotlight, open to all.

This organization brings awareness for patients who do not have any obvious outward signs of disability. Well managed by people with the best intentions in their heart.

Invisible Disabilities Association really cares about the individuals they advocate for and work hard at making a tangible difference.

I am honored and thrilled to be a part of the invisible disabilities association team. I myself have lived with and invisible disability for 18 years & quite frankly, awareness is lacking for this community. A large percentage of T.B.I. sufferers live on disability. The cost to get therapy and get some recovery is not covered by western insurance,
Many invisible disabilities do not have a standardized treatment program therefore therapies. etc. are not covered under western medicine insurance. The therapies, treatments must be paid cash out of pocket. Cost for recovery is hundreds of thousands of dollars, up-ward of a million dollars. The invisible disability association is bringing awareness and education to the community. It is my hope as a member of the IDA committee to bring so much awareness to the millions of people living with invisible disabilities that we can get the therapies, treatments & recovery work needed for people living with IDA'S..... acknowledged , accepted and covered by western medicine insurance. the invisible disabilities association is a much needed organization that deserves to be main stage in our country , helping the millions of americans who live with I.D.A.S have a voice.

Amazing work, facing an uphill battle to change hearts and minds.

I find the Invisible Disabilities Association to a be credible and friendly source for help for encouraging people living with Invisible Disabilities. The hearts of the founders and people involved with IDA are amazing! They connected me to resources and people that can help and support me navigating the pain and struggles of daily living with an invisible disability. Thanks for all you do IDA. And for BELIEVING me!

IDA has been a great resource, and gives me opportunities to work with my kid. They let me know that I’m being heard. I’d recommend them whenever I get the chance.

LOVE this organization. Was so touched by all of the efforts that went into their 2018 gala. They talked about how
Alaska has taken their logo to designate those with invisible disabilities on their state drivers licenses. We need this everywhere! Thanks to Wayne, Sherri, and all of their ambassadors for this organization.

Great organization run by truly compassionate people. No matter your illness or condition, IDA will ensure you find a home within this community.

I have been totally impressed with the Invisible Disabilities Association. It is a great organization that focuses on segment of the population often overlooked. It is so much easier to raise awareness when a person looks sick or is clearly unable to handle life tasks.
When these symptoms are invisible, it is so much harder. This group is professional, focused and dedicated to helping those people. I have had the opportunity to meet with Wayne Connell and was moved by his dedication and commitment.

IDA helped me find resources and a community, it has helped my daughter cope with her Invisible disability!

I am really disappointed that the Invisible Disabilities Association has chosen to retain their incorrectly granted trademark for "Invisible Disabilities" rather than instead pursuing a trademark for "Invisible Disabilities Association". The phrase "invisible disabilities" has been around for many decades, is embedded in the ADA, and is an important identity marker for many of us. There are three trademark symbols on the cover photo of this page alone! this is absurd. I am an academic working in disability studies and "invisible disabilities" are part of my identity, not a phrase for corporations to profit from or limit the usage of. This is a gross misuse of trademark law and very sad to see from an association whose supposed purpose is to benefit us.

I have worked with this organization for over 6 years and watched it grow and reach thousands of people with chronic pain and illness or have issues that you cannot see but are reminded daily of their disability. This organization provides a great resource for both the care giver and the person dealing with their issues - it offers support and resources to improve your life.

I have been associated with Invisible Disabilities Association for many years. I have mostly attended the yearly Gala and was a volunteer for 2 years to help with the Gala event.
This organization has helped encourage and inform countless hurting people about how to
care for friends and family members who have an invisible disability. The leaders of this organization are very caring people who are motivated by love and doing things with the highest quality.

Each year I am amazed at the energy and tireless devotion invested by the leaders of this organization and how tenacious they are at overcoming obstacles and problems associated with running a people focused organization. Every year there are quite a number of caring volunteers and committed businesses that I noticed put in a big effort because they love people and believe in what this organization does and stands for.

If you struggle with an invisible disability or a family member who does - you are not alone. I highly recommend that you take an open and honest look at the people that run this organization and you will find that they are very honest and loving people who do not have any secret agendas or selfish motivations. They simply want to bless others.

They have certainly blessed my life and opened up my heart to care for others better.

Sincerely,

Randy Stanton

I have been volunteering for the IDA for nearly ten years now and have seen the dramatic impact they make on the community. This is such an underserved audience, and IDA is living its core values daily, fighting to give a voice to people who otherwise may not have one, or be misunderstood.

This organization is a true non-profit and re-invests any dollars back into the organization's aggressive awareness mission. All volunteer board of directors, comprised of senior executive professionals aligned with the Founder's vision.

I have been a volunteer with IDA since 2012. I have seen firsthand the positive impact that IDA has on those touched by invisible illness and disability. I am one of them. IDA seeks to bring understanding and awareness about invisible illness to family members, friends, caregivers, and anyone touched by ID. EVERYONE has a story-- we all know at least one person who is dealing with an illness or disability that does not show on the outside. I continue to get inspiration from the thousands of people who have found encouragement, understanding and other support not only from IDA, but from our support communities and from one another. We have worked hard to raise awareness, through our online communities, recognition events, and the growing ID community who participate in the annual Invisible Disabilities Week in October. I hope that through our programs, and through the generosity of those who give their time, tell their stories, and contribute to IDA, we can continue to encourage, educate and connect people worldwide. I am proud to be affiliated with this organization.

This organization puts its constituents first in everything they do.

I have been living with a rare eye disease since the age of 5, going into the hospital monthly to get steroid shots in my eyes. At the age of 12, I lost sight in both of my eyes. Three months later I gained partial sight back in my right eye. In my early 30's I was diagnosed with Lupus and dealt with chronic pain. In this journey I found myself slipping in and out of the "Invisible shame" I tagged myself with. One day I was blessed to meet the founders of Invisible Disabilities Association, Wayne & Sherri Connell. They touched my life in a profound way by showing me unconditional love and introduced me to to this amazing Org.

Please think twice before donating to this organization. You are not directly helping the people most in need of help, you are helping the association to sell their wares to only those who can afford it and grow their company. Disgusting! Only interesting in selling their wares. They create materials that would help strengthen relationships between those with invisible disabilities and the people around them. But if you are actually disabled by your invisible disability and can't afford their helpful materials it's tough luck to you. They only want to sell, and not really help those who could benefit most from what they claim they are trying to help with. Very ugly IDA, very ugly.
They refused to help in any way with a coupon or code for books or pamphlets (for which their site store is set up for) and then wrote this... "We are a small organization with a big heart and a big reach! At this time we have no coupons and our website is at the lowest discounted rate from Amazon. We are volunteer based and therefore our small team of volunteers are working extremely hard to bring awareness, education and support to millions around the world, in addition to their jobs, families and/or disabilities.

Because we want people to have a place to share their websites, blogs and articles, we have our Facebook Page open for people to post on our Visitor Page and we have over 169,000 readers! This is also a great way to Share your story with others in our Invisible Disabilities Association Community on Inspire! We have over 4,000 members of our community and Inspire has over 750,000. Please read Inspire's Community Guidelines before posting."

Big heart?! Nope. So in other words... we can't give you any help in communicating better with your loved ones, but write for us so we can grow and sell our stuff to other people. Just ugly.

UPDATE: Received two notes from IDA today. Seems they are now reaching out to offer a few of their communication assisting materials as a gift. A very nice gesture. I will update again upon receipt. I still feel that they would best serve their intended purpose if they would have a decent percentage of donations go to supplying materials (the pamphlets and books) to the people who most need them (and can't afford them due to actually being on disability). I hope that in the future they will find a way to accomplish this.

This has helped me so much by helping me understand not only what I go through but also my friends and family! Thank you so very much!!!

I put my role as a "professional with expertise in this field" instead of "member of the general public" because there are no greater experts on invisible disabilities than those who have them. It is ethically and morally wrong for a company to trademark an identity like this. Should "white" or "black" or "Latino" be trademarked? Should "man" or "woman" be trademarked? Should "American" be trademarked? No, no, and no, and yet, "invisible disabilities" has a trademark. The Association is acting incredibly harmfully towards my community because of this.

I believe that IDA continues to provide awareness and give a voice to individuals who otherwise would be isolated and abandoned. I have been working with the founders for almost two years in an effort to expand this voice into the built environment and provide a shift in design , construction and materials selections that reflect the unseen sensitivities of IDA members .

Becoming aware of invisible disabilities has changed my perspective about many people, and my understanding of them. We have a daughter who suffers from chronic pain, and IDA has increased my awareness of her life and struggles. Of course, this message transfers to many people I know, who always "look good."

They are a great organization that truly beliefs in helping people.
Aaron

Working diligently to create a special Idea Home to educate the public about Invisible Disabilities through a home tour and educational programs!
Contact Wayne and Sherrie for more information today!
ONwards and UPwards!

How dare the IDA trademark the term "invisible disabilities." I am not a brand, and my identity is NOT to be determined by someone who is not themself a sufferer. You do not speak for us. HOW DARE YOU THINK OTHERWISE.

This organization is only interested in making money, not for advocating change or supporting those with invisible disabilities. They block criticism on their social media, and do not listen to the voices of those who they claim to support. DO NOT TRUST THEM.

This organization is trying to trademark the term " invisible disability" You can't trademark our identities!

*zero stars*
Invisible disabilities should not have to include (tm). I am a person. I have invisible disabilities. "Invisibible Disabilities" is not a name to be claimed or made up company title. The term has existed long before this org. Invisibile disability is a part of my identity. My identity, who I am, and my disabilities should not be trademarked. Shame on this organization. It clearly has no true understanding of disabilities or moral ethics.

I have several invisible illnesses, and you have no right trademarking them - you have to be pretty horrible to do such a thing.

The Invisible Disabilities Association does not connect people and organizations - rather the IDA silences people and organizations. The IDA seeks to build a wall around Invisible Disability (tm) - and the king at the center is Wayne Connell. Watch out, if you don't fit into Wayne's brand of Invisible Disability - then this organization may try to silence you.

Any organization ballsy enough to trademark a term used by so many to define their identities should also be ballsy enough to face up to their critics instead of blocking them on Twitter and refusing to answer for their actions.

Attempting to set your organization apart by trademarking "invisible disability" would be just as offensive if it was any other identifying characteristic. Having an invisible disability could mean being overlooked by the medical community, misunderstood by family, friends, or coworkers, or struggling to meet everyday challenges. Now it also means coming to terms with the fact that a very basic identifying, perhaps community-rallying label, has been co-opted by one organization.

Please choose to support literally any other organization with your time and money.

The Invisible Disabilities Association has no logical right to the term "invisible disabilities."

I have an invisible disability. This is part of who I am. My identity is not for sale.

The term "invisible disability" has been in use for about a century. The fact that the IDA were able to copyright the term drives home the point that there is too little awareness of invisible disabilities--and the IDA is profiting from this. Adding injury to insult, they drove the Invisible Disability Project off of Facebook; a community of 50,000 people. They have reportedly sent cease and desist letters to others who use this established, descriptive term. The US Government has been using this term (through the ADA, EEOC, ODEP, etc.) since long before the IDA got their copyright. Is the IDA going to sue them, too?

The IDA protests that their stakeholders and Facebook followers have not expressed concern about the trademark. Yet they block their critics from their Facebook page!

It appears that the Invisible Disabilities Association is more interested in making a "brand," raising money, and selling t-shirts than helping people with invisible disabilities.

I have multiple invisible disabilities. The man who started this organisation is NOT disabled, much less invisibly so, and is actively silencing those of us who are by sending cease and desist notices telling us not to say we have invisble disabilities because he trademarked the term -- a term that's been in use for over a century.

If you want to support people with invisible disabilities, support US, not an abled person who is bullying and silencing us!

This "non-profit" has trademarked a term in use for over 100 years, and has attempted to monetize the phrase recognition to their own benefit, to the detriment of other charities and activists who use have been using the term extensively for years. They have refused to communicate with community leaders who have contacted them in attempt to resolve this. If I could give zero stars, I would.

I cannot imagine a non-ableist argument that would rationalize how this organization has conducted itself around their recent trademarking of the general term "invisible disabilities". Simply by trademarking the term (which I've read they attempted to do once before and were denied, they were really committed to this), they cop-opted countless voices, people who use this term as a part of their identity.

IDA then reportedly used their trademark protection to silence whole groups of people, removing and blocking their access to media (Facebook takedown). And now I'm seeing how their representatives are responding to criticism from individuals in the community - tipping their hand to show an ableist, "we know what's best for you" attitude.

If you're researching IDA here because you're wondering if they are worth donating your time, money, or services to, I would recommend that you keep looking. It seems that IDA does not care about the very people they claim to represent.

The way that this organization and its representative have talked to and about Disabled people and invisible disabilities demonstrates profound ignorance of and contempt for our community, our bodies, and our political identities. Nothing about us without us and so nothing with the Invisible Disabilities Association.

This organization is clearly acting in detriment to the very people they claim to want to help. Whether this is a calculated move or a gaffe, I cannot trust them to represent me or people like me.

They trademarked the phrase "invisible disabilities"; harming the community they claim to support. They're ableist hypocrites masquerading as a "charity". Nothing about us without us!

The trademark Issued for this charity is for "Invisible Disabilities", not for " Invisible Disabilities Association", a fact that this charity has already begun to use to its advantage. They have forced name changes of other disability groups on Facebook, whilst claiming to want to bring charities together. As part of the disabled community with a non-apparent disability, I am concerned to see my identuty trademarked in this manner.

Their founder is non-disabled, and the bio presented for him focuses solely on the supposed heroism of his marrying and supporting a disabled partner. His connection to the community that this charity purports to serve is weak, as evidenced by the attacks on other charities. Very disappointed and would encourage others to donate elsewhere.

Founded by an abled man who, according to his own bio, married his disabled wife "in spite" of her disabilities and whose friends are surprised he married her because she is disabled.

If you have an organisation which purports to help disabled people, perhaps address your issues of ableism first. Disabled people are not here to be pitied, we're not here to inspire you, and we're certainly not about to support the sort of an organisation which trademarks our identities in order to profit from us whilst simultaneously shutting down any and all contact made with them in an attempt to hold them accountable.

This organisation has blocked disabled people who dare challenge them on social media and ignored countless others, immediately stifling the conversation and refusing to answer legitimate queries from the very people they pretend to support.

Finally, since trademarking the phrase "invisible disabilities", they have sent cease and desist letters to other organisations who use that same phrase, a simple descriptive phrase, which is used by thousands of disabled people as part of their identity.

Send your money elsewhere, find an organisation which does not seek to stamp out other charities and rob its potential clients of their very identities.

My identity is not for you to trademark. Don't profess to care for a group if your whole MO is to take out organisations that actually help us.

After I learned that the Invisible Disabilities Association had trademarked the term 'Invisible Disabilities', I contacted them via Twitter to ask why, as the term is not a brand, it is a disabled identity. I was blocked almost immediately. I was contacted by a member of the Association's board, whose expertise is in Strategic Communications. She felt it necessary to chastise me for complaining about the IDA and remarked that I did not personally know any member of the board. She continued to harangue other disabled people who are also upset about how our identities as people with invisible disabilities has essentially been commercialised by the IDA. The IDA has blocked disabled people from its official Twitter account. Instead of engaging with the concerns of the large online community of disabled activists and self advocates, the IDA has thought it fit to ignore us and our concerns. If a disability organisation, which is composed mostly of non-disabled board members (there is little information on its website to suggest otherwise), feels the need to wilfully ignore the voices and concerns of the people it purports to represent, that organisation cannot be regarded as working for the good of those people. It is highly disappointing that the IDA thinks itself above reproach, and seeks to silence and suppress any dissent or criticism of its practices, when such dissent is emanating from the very people the IDA claims to support.

The Invisible Disabilities Association trademarked the phrase 'Invisible Disabilities' and is now using their trademark to disenfranchise other organizations that represent people with invisible disabilities (they even got one kicked off of Facebook).

Here's the thing: This is an organization that was started by a man who does not have an invisible disability, a man who had made no efforts to integrate himself into the invisible disabilities community, and now he's making demands with an incorrectly issued trademark.

They may have the name, but they do not represent us. Please give elsewhere.

I have lived with a disability my whole life and struggled feeling invisible and not heard. I was blessed to meet the Connell's in my 20's and volunteer for this amazing organization. I have watched IDA reach and touch so many lives over the years and am truly grateful to be a part of such a wonderful group of people. I am now working part time with IDA and couldn't be more proud. Invisible no more!

I have volunteered with IDA for many years and am so grateful to be involved with an organization that truly believes the stories of people living with chronic illnesses and provides much needed support and encouragement. IDA also reaches out to caregivers, employers, friends and family members that need education, support, and resoures to understand the struggles of those living with these invisible illnesses. What a privilege to be part of an organization reaching out to shine a light to make people feel invisible no more!

I am always strengthened when I read stories or watch videos IDA makes available through social media. I love being a part of an organization that not only touches people, but is seeking to develop new ways to help people struggling with invisible disabilities.

IDA exists to help bring awareness, education and support to millions who live with illness, pain and injury. There are so many out there who feel there is nobody who understands their disabilities and struggles. Countless people who feel abandoned and lonely, now know that they are understood and lifted up by IDA and the connections they have made with others who "get it." I am so thankful for the most dedicated and talented Board Members and Volunteers who understand, believe and care! We have a great IDA Team!

This organization not only provides community to those who are going through life suffering invisibly, but it also provides information and support that can be crucial to helping those around people with Invisible Disabilities to better understand what they are going through and how to better do life with them.

They are an incredible resource for families and individuals. Check out their upcoming brain symposium. It is packed full of world rebound speakers, and for students and vets offered at at a discounted rate with CEUS available. Lacey Berumen

I have had Peripheral Neuropathy since 2006. I then experienced Thyroid Storm ( Graves Dz) in 2009 causing Hypertension and diabetes. My Neuropathy is in my feet and hands causing me to suffer pain that is only relieved by Gabapentin and Cymbalta. If I forget or delay my meds, I suffer! My balance is affected, my hand grip weakens and I sometime drop things ie: glasses of water. The meds cause me to have brain fog, fatigue, sequencing and short term memory loss. I suffer from blurred vision, leg cramps, burning feet, stabbing pain, and restless legs. I lost my job of 20 years, 2 years ago in Behavioral Health Admissions because I couldn't keep up the fast pace I once easily managed. I was diagnosed with Mycotoxin exposure 10 years ago due to water damage to our home which has been remediated. I have an autoimmune disorder and tested + for Lupis genetics and inability to clear toxins thru my liver like most people. I use Cholestrymine to help bind the toxins to clear thru my colen. I had my gallbladder removed due to acute non alcoholic pancreatitis last May. I suffer from Chronic Fatigue and Fibromyalgia like my mother. It has been a real battle for me. I lost my short term disability a year ago and applied for disability. I am now appealing. It has been a real financial burden for my husband and I. It's nice to know there are others out there, like me suffering these invisible diseases that are coming together to share their experiences and have an advocate voice!

I have had fibromayalgia for many years now l never relised it could be seen inviisable disability now l relise why so many people don't relise how ill it can really make a person feel and how much alone you can you can look good but feel you are breaking up iside maureen.rowley@live.co.uk

I'm new to the organization, but am excited to help spread the awareness to others living with an invisible disability. I quickly joined the Inspire group and have had some great conversations with others there who understand. This is a wonderful organization with so many great resources and I can't wait to be more involved as an Ambassador!

I found IDA via disability.gov (Wayne Connell's post) in October 2014, researched them thoroughly, explored their history and advocacy, along with their stories. IDA is THE gem in the disability area. They consistently provide high quality advocacy and support to ALL with invisible disabilities. The organization entered my life and has changed it forever!!

I love the fact that there is a global website whereas members can be in a safe and secure environment to learn, support and share experiences dealing with a variety of health issues.

I wish that more members would feel more comfortable giving general info about themselves so others can share and support more. Do not want anyone to feel pressured; however, if and when anyone feels that comfortable, Inspire's IDA is the ideal website to come to.

Inspire, thank you for this much needed website so everyone can have a voice. God placed me here on earth to be a blessing to someone else. I, then, will receive tenfold.

Again, thanks from the bottom of my heart.

Working with an organization that truly lives the dream of giving back has been superb!

Invisible disabilities are real disabilities too. This organization does a lot to help people who suffer from illnesses that are not immediately apparent. They need help and support to continue to serve others.

This is an excellent nonprofit that does amazing awareness, support, and much more for invisible awareness. I would write more but due to my invisible illness it is hard to write. Much gratitude for all their efforts!

The IDA has made such a positive impact on my life...I really cannot thank Sherri & Wayne enough! I have had serious health/pain issues for virtually my entire life, and being a part of this wonderfully caring and compassionate group is a blessing! For myself, and many, many others, whose disabilities are not "visible" this is the first time I have been part of a community that understands the unique difficulties we live with.

I have chronic pain and for 3 years now, without IDA, I would not have felt supported, loved and cared about. I have found friends through the network and they have helped me maintain a positive attitude. There is always someone who knows something about what you are going through. Without it, I would not survive in some of my darkest moments.

CRPS is something that more people should know about and chronicpaincrps.com gives so much information . The syndrome is debilitating and affects not just the sufferer but also those around them as they want to do so much more for them . The web site is brilliant in the amount of information and insight into the world of the sufferer. I hope that through reaching out to other sufferers some good will come of it

I have a neurological spinal disease called Arachnoiditis.
100s of people have told me that I don't look like I'm in pain. While I appreciate the compliments, that doesn't take away the fact that most days I spend 60-80% of the day in bed bc of the excruciating pain.
We need more awareness of Invisible Diseases!!
Thanks for spreading the word & helping others!

I live with several health conditions that have resulted in disability - none of them are visible. I live with people asking me why I must use the handicap parking spaces, when I obviously can walk. People have stopped me as I'm getting into a scooter at the store to ask me why I need to use it. Though I can spread the word that not all disabilities are visible, I can't reach more than a few hundred people through social media. The IDA reaches millions with its simple message that not all disabilities are visible. They provide links and references for people living with invisible disabilities, for caregivers, for medical professionals, and for everyone else.

I highly recommend that this message needs to be incorporated at the earliest level of our children's education. I am proud to be a supporter of the IDA.

Anything that helps raise awareness, and helps us to feel we are not alone, helps to give us hope.

The IDA has provided me with numerous links and references for groups and literature that have helped in many ways, from finding services I need to locating medical services.

I have an invisible illness and thanks to IDA, more and more people are starting to understand what it's like to have to go through it. More doctors are starting to be more sympathetic and understanding but most importantly willing to treat us. So thank you.

I follow this organization on Facebook because they provide needed information, support and a forum for people like me. I am able to tell others about my invisible disabilities and struggles, while also learning more about others like myself. We are able to give each other hope and helpful advice but most importantly to know that others care. It's heart wrenching to see how many people suffer from diseases that most people (including doctors) don't care about. Our suffering is real and debilitating and we want the world to know!

Having struggled to get support for my hidden disabilities for many years and having had to face the oppression and humiliation by institutions and individuals at the same time. I can know breath easier knowing others understand and I am not alone.

I look normal, but I have constant chronic Pain! I have been misdiagnosed labeled, and denied Medical Help. I was denied a simple accommodation so I could keep my job. I am tired of it! I found this page to be very helpful and inspiring. There are so many ignorant people out there. I have Back issues and can barely walk sometimes, yet I try to smile and act normal. I have ben denigrated, called names, repeatedly misdiagnosed, even told that my ruptured disc was a mental problem! Some of this by Doctors and Voc rehab counselors and even Social Workers! My Family even makes ignorant comments! I have pounds of MRIs and documentation, but it is meaningless. I had to fire my last PCP for not returning Phone calls and treating me like and idiot! The Misdiagnosis is still on my record, though the Doctor who Misdiagnosed me was busted for a coke problem. I have been lied about in court! By an Adult Protective services worker, who chose to look at my old misdiagnosis, illegally HIPPA would not follow up! ! It goes on and on! I have no rights! sometimes when they find out I am on SS Disability they assume I am slow, though I am mentally sharper than they are! I ask them if I should talk slower so they can understand! having this page makes me feel less alone! I have nerve damage now in my Arm, because my Doctors chose to ignore the physical symptoms and deny me an MRI! I was nearly paralyzed! I should not be walking due to the nerve damage but I ma through sheer force of will! If I did not dress and do yoga and laid on the couch maybe they would believe me. I am one of my Pain docs only patients that cracks jokes, it helps with the pain! We have no rights!

I found this group through RSDS / CRPS site. People on this site are very welcoming and supportive of everyone else. Can get advise or just helping get over a bad day. Someone is always ready with a kind word and knowing you arent alone is great. Thanks for allowing me to be a part.

I suffer from chronic repetitive strain injury that is an invisible disability with few signs of injury. It affects the nerves and, in my case, the tendons in both arms. It is extremely painful at times, and made more so due to others not seeing or understanding the difficulties that such 'Invisible' conditions present for a sufferer. The Invisible Disabilities Association has been a great comfort, both emotionally and practically for me since I discovered them. It makes all the difference in the world to know other people who go through the same daily trauma of living with an invisible illness/disability as yourself. It gives you the courage to stay positive and importantly, shows you ways of coping/managing your illness/disability in order to enhance your quality of life. They deserve recognition for the excellent support they provide to thousands of people living with invisible disabilities or illness.

before i found this group of wonderful, caring & supportive people that have many health issues they nor there Dr's understand, i'm so happy to find this group; the Gentle hugs, advise n just reading posts makes u forget about your issues for that moment, i support this group 110% n would never leave it, im so thankful for many individuals on here that support weather its good or bad;;;; feeling blessed for the Invisible Disabilities Association, thanks for being there for so many of us; Keep this group for us and so many more to join for now and the future, Thanks again- Hope Parker :)

Because of my Invisible Disability (MCS) I don't venture far from my home. Social media has become my lifeline and this group has been particularly enlightening and supportive. The members have a wide variety of disAbilities but are united in their invisibility. Comfort, advice, support, laughs, suggestions and companionship - these are things we all want and need.

Reading, getting advice, and the feeling of not being alone are three of my top reasons IDA has been a part of my life for over a year now. I am chronically ill and to look at me you would not know, except I am very thin and walk around holding my abdomen. I have gained strength and courage from other members of IDA and simply reading some of the stories. Knowing that there are others that understand bring comfort. It is important to me to have this organization, not for any contribution in a monetary sense but more for "moral" support.

I suffer from invisible disabilities. I never new a term existed to explain what I had until I discovered the Invisible Disabilities website. They do an excellent job at inclusion and offer a wealth of information and resources.

I first learned of IDA from a story in our local paper. My 45 year old son had just passed away as a result of his disabilities, mostly unrecognized by the many friends he had (Will never met a stranger). I asked memorials in his name be made to IDA, new to most people.

I am now an unrecognized 80 year old. Most people think I'm much younger, not by how I look but how I act. They don't recognize the pain I am continually in from arthritis and other problems. I believe knowing IDA and their continuing work is one of the things that keeps me going and helps me put on the face I do put on. It would have helped my son emotionally and also his children to have know about IDA and read some of their information and advice.

I feel they are a great, badly needed, and greatly unrecognized organization.

As a Executive Board member for these past several years, I'm impressed by the professionalism and passion of those involved in the organization. Integrity, Generosity, Caring are three words that come to mind. Their priority is for those who are touched by the IDA message.

As a care taker of a person with invisible disabilities myself it was easy to understand IDA's mission to encourage, educate, and connect. The organization understands the "heartbeat" of those with invisible disabilities and is excited to spread its message of awareness through social media to reach others. People with invisible disabilities need understanding, compassion, and care. This provides them hope and gives them purpose to move forward. The message we share is "a little care goes a long way." In return, everyone experiences joy in their hearts. It does not get any better than that.

I have several chronic illnesses and deal with pain 24/7. IDA has been an important part of my life. Thanks to Wayne and Sherri Connell for starting IDA, I am able to relate to others who are dealing with some of the same illnesses as myself. It's difficult trying to explain what we deal with on a day to day basis to family members as well as friends but IDA helps by putting it all down in black and white. On the outside, you would never know I was ill yet I am. Often I hear, "But you don't look sick." It gets real old. IDA publishes pamphlets that we can give out to family and friends which helps. I have given some of the pamphlets to my doctors. I continue to spread the word about IDA and in my humble opinion, IDA is one of the best advocacy organization around. It's like one big family and I would be literally lost if IDA were to ever close down. We all learn from one another and get helpful tips from our peers. IDA looks out for their members and helps in any way that they can. Due to cognitive issues, I no longer write as well as I use to - putting sentences together etc and that's where IDA helps so much. Wonderful organization for people with invisible and visible disabilities.

The Invisible Disabilities Association (IDA) reaches out to millions of people like me! People who were once active, but are now dealing with disabling illness or injury. I used to sing and dance in musicals, act in commercials, cheerlead, ride my horse, enjoy my career and I obtained 2 Bachelor Degrees. However, due to Progressive Multiple Sclerosis and Chronic Lyme Disease, at 27 I was suddenly unable to even care for my daily needs. Not only do I have to face all my losses, but the also disbelief from people who don't understand how much I want to work and care for my own daily needs, because to them I "LOOK" fine. IDA stands behind me and provides helpful booklets and pamphlets for my friends and family. They also have great articles, videos, resources and support where I can meet others batting debilitating conditions.

i have MS and Sherri is a part of my family --- literally! i love her and know the daily routine... i have MS as well and there are good and there are bad days. so many in this world that are not dealing with any kind of 'invisible' disease(s) have no clue how are days are from beginning to end. the message needs to be brought to the public and they should not judge. xo...

So many people have invisible disabilities and suffer, not only from the medical condition that they have, but also from the behavior of friends, family, associates, and strangers who don't believe what they can't see. The Invisible Disabilities Association gives a voice to all of those who need support and help, even though it isn't apparent to others.

how do I start this IDA is a lifeline for me providing support caring and understanding even when people do not understand what all I am going through they are still there for me to listen offer encouragement and moral support to difficult times in my life , I do not know what i would do without the things IDA has done for me

Being a victim of CRPS/RSD, I have the worst pain you can imagine, everyday, every minute of every day. People look at me & stare, why is this young pretty woman parking in the handicap parking space? Why is she using a walker? She doesn't look "sick"! Without a place like Invisible Disabilities, the awareness of howwe who suffer from chronic pain/illness, we can get lost. Believe that you are the only person who feels this way. That NO ONE UNDERSTANDS. Thank you Invisible Disabilities for being here for us, those who may not look" sick or disabled". Giving us a voice and creating awareness and education about us!

People are suffering all over the world with disabilities and chronic, never-ending pain. IDA is raising the awareness, offering support and encouragement to those that suffer. I applaud and praise IDA for their tireless efforts and accomplishments.

I am someone who suffers from multiple invisible disabilities. I have a service dog who assists me through life more than most of the public can understand. I have been turned away from housing, restaurants, and other public places because I don't appear to be disabled. Finally, I have a voice through the Invisable Disablities Association. The public needs to be educated on ALL disabilties, not just the visable ones. Our rights are being violated and I think the IDA will finally protect them. I have nothing but the utmost respect for what they are doing for myself and all the other people out there suffering from invisable disablities. They are ultimately saving lives by bringing awareness to this immense problem. All I can say to them is thank you from the bottom of my heart!!!

Invisible Disabilities Association provides a great network for people who otherwise would struggle to find feelings of community. Lives touched by disability are made easier and more enjoyable because of this amazing foundation.