Disclaimer

All opinions and views stated on this site belong solely to Corina Lynn Becker, and do not represent or reflects the views and opinions of any organizations, unless otherwise specified.

Thursday, January 6, 2011

Poverty and Affordable Housing

This may seem a bit off topic-ish, especially with the news about Wakefield going on. To be perfectly honestly, I'm not entirely surprised that he's been found to have changed the children's data and it really hasn't changed my opinion about him (see The Triggering of Wakefield). So I'm going to continue on and address an issue that affects a lot of people, not just Autistic people.

Poverty and homelessness is an issue that face Autistic people, as well as people with and without other disabilities. A concern for those with disabilities is whether homeless shelters, women's shelters and other services are supportive of their disabilities, and uncertainty may be a big factor in whether disabled people access such services. Which kinda creates a cycle unless it's specified that services are accessible to disabled people.

My government has been working to create unique programs and services for people with disabilities specifically. One of these has been the Ontario Disability Support Program (ODSP), a social assistance program that provides the basics: a little over $500 for living costs such as food, telephone, etc, and up to $450 for rent, per month. It's basically a safety net for people with disabilities if they are between jobs, or recovering from a bad period, and the program even includes an Employment Support services, and will cover some additional medical costs, such as service dogs, diabetes supplies, breathing machines, etc.

For the other services it doesn't cover, being on ODSP qualifies people to other programs. There's a lot of paperwork involved, of course, and it requires people to be as productive as possible while describing their worst days. But one of those programs in my city is the centralized housing list for subsidized housing, since $450 doesn't get you a decent place to live in this area.

The problem is that there's a lot of people on that wait list. My city does a magazine, profiling restaurants, venues, and highlighting city issues. In the latest issue, it reports that as of July 2010, there are 1,133 applicants currently waiting for access to social housing. With the given rate of vacancies in the city, it can take at least six months for a three- or four-bedroom unit, or up to eight years for a single-room unit.

Obviously, there needs to be more available units and in the magazine article, the issues surrounding making decisions on where to build mixed-income housing is discussed. However, due to various difficulties (such as the city's own zoning and building restrictions), it can take up to eight years for many housing units to start being built. In the meanwhile, there's still a lot of people waiting for places to live and call home.

I faintly recall a few years ago a plan to start a portal subsidized housing. The idea is that people on the housing list can find a place to live on their own and get off the housing list a lot quicker.

It's like this: say I'm on the housing list. I've gone through the application process and have been approved for social housing. Instead of spending eight years couch-surfing or hopping between shelters or enduring abusive situations, I can look around for a place that meets my needs.

After some looking, I find a nice apartment that's easy for me to access the public transit system, a grocery store, as well as other services, or at least to be able to get to other services. I'm on ODSP though, and can only afford $450 a month, and the apartment is $750 a month.

I talk to the landlord/lady/person, and make an agreement with him that he'll hold the apartment while I apply to the housing list. Then I fill out a form, asking for support for the other $300 for rent from the social housing program. The landlord/lady/person and I fill out the details of the place, sign it, and submit it. If everything checks out, the housing list approves of it, and there you go, I have a place to live and I'm off the housing list a lot quicker.

Of course, I don't know all the specifics that this would have to be put into place, but I think it's better than a waiting game where one never knows when they're going to have a place to live. Also, it gives the people a sense of respect, dignity and control over their own fate.



Edit: minor editing over the difference between rent and ODSP; I really can't do math in my head.

Friday, December 31, 2010

A year in review: 2010

It has been a pretty intensive year, so busy that I think I missed the first anniversary of No Stereotypes Here!

About this time last year, the board of directors and myself at the Autism Women's Network was preparing to launch the website for the first time. Since then, it's been non-stop excitement working on various issues. I'm actually surprised I found time to blog and keep track of it all, especially with the new DSM drafts, our board members working with the White House, and the whole Pepsi refresh contest. It's a lot to try and keep up with and blog about.

As for my own events, it's been a little tipsy turvy, with two moves, the drama of new house mates, the usual fussing over medical issues, and my own personal studies.

In the beginning of this year, I had been studying in a Library and Information Technician program, but after all the blogging I've been doing, I decided to sit back, give myself a summer vacation, and think.  I thought about being employed, and how much energy and resources that would cost me.  I thought about trying to balance work with what I do the most, writing.  Writing novels and writing about Autism.

And then I made another decision.   I decided that I would be perfectly miserable if I could not write, and was not involved with Autism issues.  And if I was miserable, I would be setting myself up to fail, crash and burn out, over and over again.  And I do not like those experiences.

So I decided to dedicate myself more to Autism and disability issues, and to educate myself more.  Because it's all good that I sit here and write my opinions and thoughts, and I hope that even that has made a difference for at least one person.  But I'd like to try and make a large difference, because I see things that don't seem right, and I don't see anyone stepping up to change things for the better.  And to do that, I need to know more things about how to make changes in my own country, province and town.

And so, I applied for the Disability Studies program at Ryerson University.  Earlier this month, I was accepted and am preparing to take courses on-line, starting in January.  For me, this is a big and exciting step towards being an active citizen, despite financial difficulties. I hope that I'll be able to share with all my readers the things that I'll be learning, and how I plan to apply them to practical use. 

As the year draws to a close, I think back on what has happened on this blog over the year, the success of ASDay, and everyone I've met online.  And I think about the year to come with hope that as good as this year has been, that next year will be even better!!!

Happy New Year everyone!

Saturday, December 25, 2010

Merry Christmas!

Two characters from my webcomic Amhelaki and I want to wish you all a Merry Christmas and a Happy New Year!

Friday, December 3, 2010

Recipes for Autism Hope

I'm going to be extremely honest; there are some things about myself I don't like, and one of them is how I'm still angry and hurt over the Autism Speaks "Autism Every Day" video, especially the parts with Alison Singer.  However, I understand that she's changed, left Autism Speaks, and started the Autism Science Foundation.  Recognizing this, I am working towards healing the hurt I feel and beginning the process to forgive her.  I hope that one day I'll be able to fully forgive her, and I am very glad that I've made this decision.  

Because really, there needs to be more science-based knowledge about Autism, and I think that the Autism Science Foundation plays a key part in "providing funding and other assistance to scientists and organizations conducting, facilitating, publicizing and disseminating autism research" and contributing to Autism Awareness. 

They consider strict scientific standards and values to be essential in Autism research.  This is crucial to understanding Autism as it makes as sure as possible that the results are accurate, and better understanding means better approaches and supports in our communities.  Truly, this is one of the best gifts that can be given to families and individuals on the Autism Spectrum.

Currently, ASF is raising funds with Recipes4Hope, and every dollar raised will go towards science-based Autism research dedicated to discovering better ways to recognize Autism and implement better supports and enhance the lives of Autistic persons.

With the hope of a better future for all Autistic persons, I encourage everyone to contribute as you wish, to donate if you can, and to spread the word as far as you can.  


Monday, November 29, 2010

Meeting the Autistic Artist

I don't think I've mentioned it a lot here, but I also do quite a bit of artwork, and sometimes I let people see my work. For the past month and a half, I've had a lot of my work at the Kerry's Place Autism Services Resource Centre in Belleville, Ontario, as part of the Spectrum Art Show. I kinda started the Show five years ago when I worked for KPAS.

Tomorrow, November 30th, I'll be at the Resource Centre from 2pm to 6pm for a "Meet the Artist" event. I'm being presented as an Autistic artist and Autism advocate.

If any of my readers are in the area, and have the time, it'll be awesome to meet some of you!


(yeah, a little last minute, I know. I'm sorry)

Monday, November 22, 2010

Surviving the Holidays with Autism

Up here in Canada, we had our Thanksgiving back in October, so we're all getting ready for Christmas/Hanukkah/other winter holidays.  I'm going to be very honest: I celebrate Christmas, so my default for the holiday season is Christmas.  This doesn't mean that stuff I say cannot be used for other holidays, it's just a religious difference, use as need.


But I'm kinda using my own experiences for this, so I'm going to resort to my default of Christmas.  Also, I'm mainly addressing parents in this post, but I'm certain that some of these pointers can be used for Autistics of all ages.

But yes, the winter holiday season is approaching, and it's a very busy, hectic and overwhelming time of year, full of all the things that set off Autistics and other highly sensitive individuals.  The season is full of parties, religious events, meeting a lot of people and having relatives all crowd together, malls full of shoppers and noisy music, and regular family festivities.

From my own experiences, there's nothing really new in terms of needs and challenges, just that the time of year makes everything more chaotic and intense. Add in the excitement for a countdown, the anxiety of a lot of surprises, plus a lot of the goodies that get passed around, and it's no wonder that things get overwhelming.  The trick is to manage the new sources of over-stimulation and stress while still participating in the holiday so that everyone can enjoy.

Social:
The holidays are filled with meeting people, lots of relatives, crowded house, parties, and other social complications that can make the basics, such as manners for receiving presents, more difficult to remember and perform.

Please keep in this in mind when interacting with others, that even if you know an autistic that is capable of being more polite, the overwhelming pressure on their social skills (and other skills) may mean that they are functioning on a lower level than their norm.  It may be taxing for them to remember simple Please and Thank Yous.

Be mindful of this, and be patient.  Little reminders on manners are okay, but don't be too insistent, because this is a very hard time of year and keeping the stress levels as low as possible all around is a good idea.

At events where its available, explain your and/or your child's needs, find a time-out corner for breaks, be mindful but try not to freak out at little slip ups, and if you find the stress becoming too high, leave early.  Understanding friends and family won't mind too much, and you can get back to the ones who do.  There might be some grumpy faces, but catching the stress at "grumpy" is better than "meltdown", where pretty much anything can set off a meltdown.  So be very mindful of the warnings signs.

And if you think that so many events is too taxing, skip them. Take a break and pace yourselves. Friends and family members may not totally understand or be happy about it, but you're taking care of both your autistic child, and/or yourself.  You could have a relaxing night at home, everyone doing a relaxing activity, maybe do something special if you think everyone can handle it.

I know that there are events that you can't skip, like certain religious events, or that mandatory company party.  And to be honest, some of those are, well, boring for kids, and overwhelming in general, especially if it's formal (see sensory below).  But don't be afraid to find a babysitter and go, even if it's for a little while so that you can fill the "I attended" requirements.

As for babysitters, it's good to give them some information about autism, so they know, but don't expect them to be professional respite workers.  Look for someone who is friendly and flexible, and maybe have them meet the kids a few days in advance, if it's a new babysitter, so that everyone knows each other and you can see whether they get along. My parents tried to keep the same few babysitters, so even if there was an emergency, my brother and I would know the babysitter.

Also, parents, don't be afraid to take the time to go off by yourselves and have a night together.  Everyone needs a break every once in a while during the holidays.


Sensory:
You probably could name quite a few sensory issues we Autistics have this time of year, as every thing becomes more intense, and we tend to react more because of that.  I'm talking the crowds in mall, the rushing here and there, all the loud music and holiday jingles, strange and new foods, smells and textures, and winter clothes.

Again, a lot of it is the same issues each of us have, just more intense during the holiday season.  As a result, it may be better to plan shopping trips for times when it's not so busy, or if that's not possible, to shorten the trips as to accommodate a lowered tolerance limit.  It'll probably mean more trips, but it might also reduce overload.

Another sensory issue is foods, and there are many strange things to eat, with rather strange names.  Don't worry about having your autistic test new foods; while it's certainly an opportunity to try new things, it may be more that they can handle during the holidays.  If they consent to try a bite of something you think they might like, awesome.  But be okay if they decide not to try it right now.

As for music, if you want to have it on, keep the volume down.  If there's people over, well, you might want to just turn it off, because it becomes another source of noise.

The final issue I can think of for sensory is clothes. For me at least, this is big challenge during the winter months.  I find that during winter, there's less moisture in the air, and so my skin becomes dry and more sensitive.  This means even more sensitive to the feel of cloth, textures, and seams, especially after bathing when water has dehydrated my skin.  Even sensory-soothing clothing can become irritants during this time of year.

To counter-act difficulties dressing due to this, I suggest bathing well in advance of events to give the skin time to hydrate and produce its own oils.

Also, in winter, fabrics are heavier, which is good for those who need more sensory input, but clothing contains more seams and restrictions of movement.  Given the time of year, some articles of clothing are necessary to wear outside. So try to use the hat, mitts, scarves and other winter gear that your child seems able to wear the longest, but when possible, limit the amount of time they need to be wearing their gear.

As for the times where formal wear is required, it becomes a matter of how much your autistic can tolerate.  Try to buy formal wear that can be worn for long periods of time, or else bring along a spare set of clothes, just in case.  Otherwise, let your child wear what's comfortable and looks good.


Schedule:
Another source of distress during the holidays is the deviancy from our regular schedules.  Understandably, there's a lot of things to keep track of, and it can get very busy and overwhelming.  What I think is key is keeping as much of the regular schedule, with more cool-down periods.  The normalcy of it will be grounding and calming, reassuring your autistic that things are still under control, and it helps transitioning between the holiday season and the non-holiday season.

For all the different events and activities, if possible and when appropriate, try to include your autistic in the decision making process.  This will help them to be involved and be more informed about what's happening.  This also gives them the opportunity to express what they'd like to do and experience the holiday better.

I also suggest to try to do the same things year after year; this makes the holiday a part of the yearly schedule, and as time goes on, may make the holidays easier as your autistic has a better idea of what to expect.

What I find is that after the holidays, or any big and draining events, I have a period of transition and adjustment to get back into the regular schedule. Sometimes this includes period where I regress in skills, tolerance and energy as I am recovering from the event, especially when I have been unable to maintain my regular schedule and practice skills.

During this recovery period, be patient and mindful that your autistic may be drained from the holiday, get back into the regular schedule as soon as possible, and allow them to have more quiet time periods.  For me, to recover from a weekend usually takes about a week, but it's different for everyone.


As well as what I have above, I asked my mother for some tips and advice on handling the holidays.  After all, she did raise myself and my brother, both of us with a wide range of difficulties for this time of year. So, from my mother:

1) Don't do too much on any one day; usually one event per day is enough.

2) Each morning, share that day's schedule with the kids, and only that day's schedule. Don't overwhelm them with future days and activities; stay day by day.  Also have it that the kid can carry it along and refer to it.

3) Keep clothes soft and comfortable.

4) Have quiet time, and let them know that it's quiet time, so that they can relax properly.

5) For children who have a hard time staying at the table, have a candle on the table. Makes meal times more special, and keep their attention so they don't leave.  Keep a plate under the candle, and watch for fingers that start playing with wax. (Candles are a two-edged sword; can keep kid at table, but they may want to play with the melted wax)

6) Always serve some of the kid's favourite foods at every meal, so that if they don't like the big meal they at least have something to eat.

7) Make sure that relatives and guests know the kid's needs.

8) Limit the amount of people coming over and in the house at any given time.

9) Have a safe place for your kid to withdraw.

10) If you have a large family gathering, rent a hall. But make sure to keep a safe corner.

11) Don't force the kid to do greetings and farewells; it's too much commotion in the front hall.

12) Allow your kid to choose toys to hide away that they do not have to share, but at the same time, have your kid pick toys that they do have to share with other children.

13) If playing music in the background, have calm music and be careful of the volume.

14) When opening gifts, clean up the boxes and wrappers as you go, so that it's not too chaotic.  After opening, take gifts to each person's respected places to keep the central space calm.

15) If the kid like puzzles, create a puzzle corner where they can interact with others one-on-one as they work on a puzzle.

16) Find some way that the child can contribute and make the holiday their own.  Give them suggestions and work together on whatever the child chooses, such as help decorate, help making food, setting the table, putting stamps on and licking shut Christmas card envelops, etc




If you have any questions about this list, or you think I've missed something, feel free to ask and comment.




Merry Christmas and Happy Holidays!

Monday, November 15, 2010

Preservating for Causes

While I'm pretty sure it can be annoying in some situations, preservating and being stubborn or determined can have some benefits.  One being keeping at competing in contests for a long time, such as how the Autism Women's Network has kept in the Pepsi Refresh contest for so long. 

Yes, I blogged about this some time ago; however, AWN did not make the top ten then, but since then has kept in the top 100 and kept in the running.

This month, AWN started at rank #5, and has slipped to #12.  With the combined help and voting of the community, we can get back up into the top ten and finally be able to run the workshops and programs that this funding hinges on.

As a reminder of what AWN is planning to do with the money, here's the project profile on the Pepsi site.

The Autism Women's Network is unique in that it was founded by women on the autism spectrum. Our mission is to provide effective supports to autistic females of all ages through a sense of community, advocacy, and resources.

AWN's Project FAIM (Female Autistic Insight Mentoring) workshops will be the 1st of its kind.

We plan to set up 5 Project FAIM Workshops across the USA which will focus on qualities specific to females on the autism spectrum. Topics will include: peer supports, adolescence, adult life, relationships, vulnerabilities and successful communications.

Project FAIM Workshops will include active supports and information for everyone (autistics, parents, educators, etc.)

The participants will meet renowned autistic females whereby gaining valuable insight.


We will secure the Autism Women's Network non-profit status so we can continue to provide Community Events, online Forum support & E-Mentoring as well as our AWN Radio Show.

Please help us to continue to support Autistic females who may not have access to supports and accommodations otherwise.  The workshops may be a small step towards a greater change and difference in many women's lives.

Thank you very much.



(Please pardon the decreased quality of my writing in this post; I am having some communication difficulties today)


(Disclosure: Corina Becker is the Director of Networking for the Autism Women's Network.  However, all opinions and views expressed on this site are solely the property of Corina Becker and does not reflect the official view of AWN and other organizations unless specifically stated. )