Life as a continuous learning experience

As health care professionals it is extremely important that we stay up to date on the current evidence to support the treatment approaches we are using in practice. In addition to that, we also want to make sure we are listening to the needs of the populations we are working with.   

You might be asking, well how can I make sure I stay on top of all the research and evidence? And how do I make sure I hear the voices of the communities I am working with? Well there are many resources out there that can help you!

The first thing I would recommend is making sure you are subscribed to your national organization as they are constantly updating their website and disseminating new research related to your field. For example, my national organization is the American Occupational Therapy Association (AOTA). Typically, organizations have annual conferences that showcase the current evidence supporting new intervention approaches.

Next, I would also recommend you figure out if your state has any organization related to your field. Illinois has the Illinois Occupational Therapy Association (ILOTA). I personally enjoy being involved with this organization because they have local conferences that I can easily attend.

Over the years I have also come across some unique programs that have a variety of online trainings and resources for practitioners. Here are some of the ones I frequently check:

1.      Early Intervention Training Program

o   They have several free online webinars that can be useful for individuals that are working in early intervention or are considering going into this practice setting

2.       Association of University Centers on Disabilities (AUCD)

o   AUCD offers several events and webinars open to the public

In terms of making sure you are listening to the needs of your population, I recommend building a connection with an organization that serves your target audience. For example, my area of interest is pediatrics and families. I have recently started volunteering at two community organizations that work with families of children with disabilities. With just a few sessions of interactions I have been able to identify areas of need that they have and ways in which I can assist them. One organization I want to highlight is:

1.      Grupo Salto

o   Grupo Salto was started back in 2005 with the intention of providing supports to Spanish-speaking families from Chicago who have a child with autism. The goal of Grupo Salto is to empower families and be advocates for change. The group meets monthly to provide educational seminars and social activities.

o   They have their 1st Disabilities Conference in Spanish coming up on April 6th, 2019. There are many ways in which you can get involved to make this a successful event! Contact them via gruposalto@gruposalto.org

Remember, although you may have completed, or are in the process of completing your educational requirements to be a health provider, there is an abundance of knowledge that we can still learn from on an everyday basis! I encourage you to read a new article, a new blog, or listen to a webinar at least once a week!

Jazmin Landa

The Government Shutdown: A Debacle for All, Especially Individuals with Disabilities

According to the Washington Post, approximately 800,000 federal government employees have been impacted financially by the partial government shutdown resulting from the Congress' inability to agree upon a budget. While Congress debates over one controversial issue - the inclusion of funding for a border wall, the effects of the shutdown creates more issues and ceases the services and supports that already have bipartisan and taxpayer support.

Members of the Disability Justice Initiative and Center for American Progress describe five ways the government shutdown is impacting individuals. One is obvious, during the shutdown many government workers do not get paid, but in some "essential" cases must still work. What may not be obvious is that finding part-time or alternative work in the mean time for individuals with disabilities can often be challenging. This is especially true for contracted workers or individuals who are working for the government as part of community-partnerships specific to individuals with disabilities. Second, a lapse in USDA funding has left individuals dependent on SNAP, WIC, free/reduced school lunch, and CAFCP funding with uncertainty in regards to how long they will have benefits. According to the Food Research & Action Center, "food insecurity disproportionately affects people with disabilities. In 2009-2010, households with adults living with disabilities experienced a food insecurity rate of 33 percent — almost three times the rate at which households with no adults with disabilities were food insecure (12 percent)." The organization states that one in five households receiving SNAP benefits includes an individual with disabilities. Another impact of the shutdown relates to housing. According to the Center for American Progress, the U.S. Department of Housing and Urban Development (HUD) is shutdown with a lapse in funding, putting at-risk the rental assistance programs that provide supportive and safe housing for more than 5 million low-income households. According to HUD, approximately 20 percent of individuals that receive HUD rental assistance have a disability. Lastly, it is important to remember that many state and local programs rely upon federal funding. If the government shutdown results in a lapse in funding for these programs, transportation, healthcare, Head Start programming, public transportation, and more could be impacted. Individuals with disabilities often utilize such programs. In fact, according to the National Council on Disability, 6 million Americans with disabilities have difficulties obtaining the transportation they need and utilize public transportation services.

As we move forward, it is essential we continue to communicate to our legislature the impact that the government shutdown is having on all of us, including individuals with disabilities. While the "major" issue that has initiated this shutdown is controversial, the services and supports that have ceased or are at-risk of ceasing are common sense and withholding them is cruel.

 

Michelle M. Sands

University of Illinois at Urbana-Champaign

Doctoral Student - Department of Special Education

msands4@illinois.edu

 

How to Talk to Someone Who "Can't Talk"

Whether it is at work, school, or out in the community, it is almost a guarantee that at some point in their life, everyone will meet someone without the ability to verbally communicate. This characteristic can occur in all sorts of populations for all sorts of reasons. These populations can include individuals with autism spectrum disorder, individuals with cerebral palsy, stroke survivors, traumatic brain injury survivors, individuals with neurodegenerative disorders, and many more. Because of this variety and likelihood of a rendezvous, it is very important for everyone to know how to handle this type of interaction appropriately and pleasantly.

A common misconception is that if someone can’t talk, there is no way to communicate with them. That’s incorrect! Just because physical speech isn’t present in an individual, that doesn’t mean they don’t have the ability to hear and understand you, as well as form their own thoughts, opinions, ideas, and judgments of your character. Watch yourself!

In order to avoid offending someone, here are some tips to consider when communicating with individuals who are unable to verbally communicate:

●       Always assume competence! It is very frustrating to have communication difficulties, and even more frustrating when others don’t think you are capable of something.

●       Use vocabulary, intonation, and topics that reflect the individual’s age, not their physical size or appearance. Some neurodevelopmental disabilities such as Rett syndrome or Down syndrome may cause a smaller stature, so a 10-year-old girl may physically appear to be 4 years old or younger. She’s still a 10-year-old with 10-year-old interests, so if you talk to her in your preschooler voice, she’ll most likely be unhappy. If you’ve just met someone and are unsure of their age, just do your best!

●       Pay attention to body language, particularly facial expressions. Although someone may be unable to tell you out loud that you’re scary and that they want space, a sharp glare can say a lot. Respect that!

●       Don’t use physical touch too much unless you know it is something that this individual enjoys. How would you feel if you were 15 years old and someone came up to you and kept touching your hair? Yikes.

●       Don’t talk about the person directly in front of them. This generally isn’t a thing you should do to anyone, ever, so definitely don’t do it to someone just because they can’t verbalize their annoyance. If you have questions or comments, direct your conversation toward the person! Inclusion is key.

Although these tips just scratch the surface, hopefully they will be helpful in the future. If you’re looking for more, here is a great source for communicating with individuals without the ability to speak within the clinical setting: https://bronwynhemsley.wordpress.com/about/25-tips-for-communicating-with-people-with-little-or-no-speech-in-clinical-settings/ 

Anna Hastings