Auteur : adminWP

  • From a autistic teenager parent

    From a autistic teenager parent

    From an autistic teenager parent

    2–3 minutes

    From a parent

    My son was diagnosed with ASD when he was 14 years old.  As a toddler, he had some language delays, which I attributed to him being in a trilingual environment.  When he was 3 years old, the educators at his daycare remarked that he often stood on the side observing rather than getting involved when animators from the outside came to do dance and theatre classes.  Nobody, except me, talked about autism at the time, in fact the daycare providers assured me that he showed no signs of ASD.  Instead we were referred to a speech-language therapist who discovered that his linguistic comprehension was at a very low level.  The language therapist worked with him until he started kindergarten and he made great progress, to the point where they saw no need for any additional support when he stared school. He went through elementary school without any problems and had a good group of friends. It was only when he started high school that things got really challenging both socially and academically and finally he himself asked to be evaluated for ADHD, which led us to the ASD diagnosis. 

    school, corridor, locker, night, darkness, locker, locker, locker, locker, locker

    If I had known at an early age that my son was on the spectrum, we would have saved ourselves tons of frustrations over the years and would have had a better understanding for his rigidness, refusals to wear clothes that he was not used to, his tantrums when a playdate was over etc, etc. We also would have been able to seek professional help to better prepare him for high school and to work on things which are challenging for him.  I knew very little about ASD before he was diagnosed.  Over the years, I had seen signs of ASD in my son but I did not understand the implications of being autistic and the challenges and micro aggressions that everyday life poses to an autistic person.  I believe my son is good at masking but it eventually led to an autistic burnout where he was no longer capable to go to school or even attend family gatherings.  If we had been aware of the diagnosis earlier, I could have read up on ASD, look for support groups, and have started to navigate the system to find resources and help.  If you as a parent have just learnt that your child is autistic, you may be overwhelmed with emotion and, possibly, denial or doubt about the diagnosis.  I believe however that the fact that you now know that your child is on the spectrum, will allow you to be open to learn more about it and to become better equipped to accompany your child.  It does not mean that you need to look for signs that may not be there or that you have to start parenting differently, it will simply widen your horizon.

  • La différence invisible – Éli

    La différence invisible – Éli

    Eli, femme AuDHD, diagnostiquée à 26 ans

    Au moment où j’ai lu son histoire, j’avais aussi 27 ans et je m’adaptais à une diète sans gluten (et bien sûr, j’ai un chat). Mon expérience est un peu à l’envers de la sienne. J’ai réalisé en maternelle ma différence, mais j’avais l’énergie pour masquer mes émotions et mes besoins (tout pour plaire) jusqu’à ce que je développe la maladie coeliaque (sans gluten) à 24 ans. Les difficultés que j’avais avant sont devenues ingérables, particulièrement les stims auto-destructeurs (arracher mes ongles). À ça s’ajoute de nouvelles sensibilités sensorielles. Je pensais devenir folle. Avoir le diagnostic TSA a été un grand soulagement, mais c’est lire l’expérience de Marguerite qui m’a mis sur le chemin de l’acceptation de soi. Je me suis achetée un bon casque anti-bruit :)

    La différence invisible

  • La différence invisible – François

    La différence invisible – François

    François, homme AuDHD, diagnostiqué à 53 ans

    Ma femme et mon père l’ont lû. Un très bon cadeau. L’album parle du sujet de façon abordable avec humour et sensibilité. Il m’a permis d’améliorer mes relations avec mes proches. Ce que j’apprécie le plus de l’ouvrage est comment il se lit facilement. Pas de statistiques, seulement du vécu.

    La différence invisible

  • 1-Qu’est ce qui vous a mené vers la démarche d’un diagnostic dans le spectre de l’autisme?

    Témoignage

    François Dionne

    1–2 minutes

    1-Qu’est ce qui vous a mené vers la démarche d’un diagnostic dans le spectre de l’autisme?

    Mon diagnostic m’est venu complètement par surprise. Mon psychiatre m’a fait faire un test et quand j’ai reçu le résultat, surprise!

    Leave a Reply

  • Témoignage complet sur le processus diagnostic – François Dionne

    Témoignage

    Témoignage complet sur le processus diagnostic
    François Dionne

    1-Qu’est ce qui vous a mené vers la démarche d’un diagnostic dans le spectre de l’autisme?

    Mon diagnostic m’est venu complètement par surprise. Mon psychiatre m’a fait faire un test et quand j’ai reçu le résultat, surprise!

    2-Quelles ont été vos craintes, difficultés et appréhensions durant la démarche de diagnostic?

    Ma réaction a été la surprise. J’avais passé par trois phases. La première: « ah ouin??? » (surprise), suivie de « Ouiiiiin! » (soulagement de voir que ma condition a un nom) et finalement, « ouin! » (acceptance de ma nouvelle identité).

    3-Qu’est-ce qui vous a aidé, soutenu ou supporté durant la démarche de diagnostic?

    Un psychiatre qui me respecte et m’impliquer dans la communauté.

    4-Comment avez-vous obtenu le diagnostic? (Nous acceptons l’auto-diagnostic.)

    Mon psychiatre m’a fait passer un test.

    5-Comment vous sentiez-vous avant, pendant, et après la démarche de diagnostic?

    Ma réaction a été la surprise. J’avais passé par trois phases. La première: « ah ouin??? » (surprise), suivie de « Ouiiiiin! » (soulagement de voir que ma condition a un nom) et finalement, « ouin! » (acceptance de ma nouvelle identité).

    6-Comment décririez-vous l’autisme, qu’elle serait votre définition, votre façon de l’expliquer simplement dans vos mots?

    Être auDHD, c’est comme être l’enfant d’un Vulcain et d’un Klingon. J’ai deux natures opposées que je dois réconcilier pour assurer mon bien-être. Mon coté Vulcain est l’autisme tandis que mon coté Klingon est mon TDAH.

    7-Quelles ont été vos craintes, difficultés et appréhensions après le diagnostic?

    En réalité, je me suis senti soulagé et libéré. Mon ancien diagnostic était la schizophrénie paranoïde. Je l’avais reçu en 1989, quand la science médicale n’était pas aussi avancée. C’était comme si j’avais appris que je suis un zèbre normal au lieu d’un cheval raté.

    8-Qu’est ce qui a manqué durant la démarche, ce que vous auriez eu besoin?

    Des outils pour gérer mon TDAH. J’ai été très organisé durant mon enfance: mon lit était fait à chaque jour et ma chambre était en ordre. Je ne sais pas ce qui est arrivé à l’âge de dix ans mais j’avais désappris mes bonnes habitudes. C’était peut-être le début de mes troubles mentaux. Je suis en train de réapprendre mes bonnes habitudes. J’ai peut-être besoin d’un ergothérapeute qui connait la neurodiversité.

    9-Qu’est-ce qui vous a aidé, soutenu ou suporté durant la démarche de diagnostic?*

    Ma curiosité, mon goût d’apprendre et mon sens de l’auto-critique. J’ai dévelopé une fascination pour ce microcosme qui se trouve entre nos deux oreilles. Je dirais aussi mon sens de l’autonomie. Je crois fermement que la santé est une responsabilité aussi bien individuelle que collective.

    10-Quelles ressources vous ont semblé pertinentes pour vous? Partagez-les avec les utilisateurs! (Organismes, site web, vidéo, livres etc.)

    « The Bullet Journal Method », de Ryder Caroll. Je ne jure que par ce livre. Écrire un journal m’aide grandement à mettre de l’ordre dans mes pensées. Je préfère le papier au lieu des méthodes digitales car écrire à la main fait travailler davantage le cerveau que tapper sur un clavier d’ordinateur ou de téléphone. Le papier ne m’expose pas aux écrans, qui aggravent ma cyberdépendance.

    11-Avez-vous des recommandations pour ceux qui sont en démarche de diagnostic actuellement?

    Je n’ai pas de conseils qui peuvent s’appliquer à tous les autistes, à part un seul: connaissez vous même et faites-vous confiance. Souvenez-vous que les docteurs sont les experts en médecine mais que vous êtes les experts sur vous-même.

    12-Quel message voudriez-vous faire passer aux personnes non-autistes?

    Je m’adresse aux docteurs: traitez vos patients avec respect. Un psychiatre qui me respecte a été la clé de mon rétablissement.

    13-Quel message voudriez-vous faire passer aux personnes autistes, surtout celles qui découvrent ou viennent de découvrir leur autisme?

    Bienvenue à bord. Sentez-vous à l’aise et ne vous gênez pas d’enlever votre masque quand votre environnement le permet. Protégez votre bulle sensorielle et respectez vos limites

    14-Y a-t-il quelque chose que vous aimeriez ajouter ou partager librement, une question pour nous, un détail à ajouter?

    Je travaille présentement sur mon blog. Il est encore en construction mais je vais vous donner l’addresse: https://journalmental.ca .

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  • 13-Quel message voudriez-vous faire passer aux personnes autistes, surtout celles qui découvrent ou viennent de découvrir leur autisme?

    13-Quel message voudriez-vous faire passer aux personnes autistes, surtout celles qui découvrent ou viennent de découvrir leur autisme?

    Témoignage

    13-Quel message voudriez-vous faire passer aux personnes autistes, surtout celles qui découvrent ou viennent de découvrir leur autisme?

    Leave a Reply

  • 12-Quel message voudriez-vous faire passer aux personnes non-autistes?

    12-Quel message voudriez-vous faire passer aux personnes non-autistes?

    Témoignage

    12-Quel message voudriez-vous faire passer aux personnes non-autistes?

    Leave a Reply

  • 11-Avez-vous des recommandations pour ceux qui sont en démarche de diagnostic actuellement?

    11-Avez-vous des recommandations pour ceux qui sont en démarche de diagnostic actuellement?

    Témoignage

    11-Avez-vous des recommandations pour ceux qui sont en démarche de diagnostic actuellement?

    Leave a Reply

  • 10-Quelles ressources vous ont semblé pertinentes pour vous? Partagez-les avec les utilisateurs! (Organismes, site web, vidéo, livres etc.)

    10-Quelles ressources vous ont semblé pertinentes pour vous? Partagez-les avec les utilisateurs! (Organismes, site web, vidéo, livres etc.)

    Témoignage

    10-Quelles ressources vous ont semblé pertinentes pour vous? Partagez-les avec les utilisateurs! (Organismes, site web, vidéo, livres etc.)

    Leave a Reply

  • 9-Qu’est-ce qui vous a aidé, soutenu ou suporté durant la démarche de diagnostic?

    9-Qu’est-ce qui vous a aidé, soutenu ou suporté durant la démarche de diagnostic?

    Témoignage

    9-Qu’est-ce qui vous a aidé, soutenu ou suporté durant la démarche de diagnostic?

    Leave a Reply

  • 8-Qu’est ce qui a manqué durant la démarche, ce que vous auriez eu besoin?

    8-Qu’est ce qui a manqué durant la démarche, ce que vous auriez eu besoin?

    Témoignage

    8-Qu’est ce qui a manqué durant la démarche, ce que vous auriez eu besoin?

    Leave a Reply

  • 7-Quelles ont été vos craintes, difficultés et appréhensions après le diagnostic?

    7-Quelles ont été vos craintes, difficultés et appréhensions après le diagnostic?

    Témoignage

    7-Quelles ont été vos craintes, difficultés et appréhensions après le diagnostic?

    Leave a Reply

  • 6-Comment décririez-vous l’autisme, qu’elle serait votre définition, votre façon de l’expliquer simplement dans vos mots?

    6-Comment décririez-vous l’autisme, qu’elle serait votre définition, votre façon de l’expliquer simplement dans vos mots?

    Témoignage

    6-Comment décririez-vous l’autisme, qu’elle serait votre définition, votre façon de l’expliquer simplement dans vos mots?

    Leave a Reply

  • 5-Comment vous sentiez-vous avant, pendant, et après la démarche de diagnostic?

    5-Comment vous sentiez-vous avant, pendant, et après la démarche de diagnostic?

    Témoignage

    5-Comment vous sentiez-vous avant, pendant, et après la démarche de diagnostic?

    Leave a Reply

  • 4-Comment avez-vous obtenu le diagnostic?

    4-Comment avez-vous obtenu le diagnostic?

    Témoignage

    4-Comment avez-vous obtenu le diagnostic?
    (Nous acceptons l’auto-diagnostic.)

    Leave a Reply

  • 3-Qu’est-ce qui vous a aidé, soutenu ou supporté durant la démarche de diagnostic?

    3-Qu’est-ce qui vous a aidé, soutenu ou supporté durant la démarche de diagnostic?

    Témoignage

    3-Qu’est-ce qui vous a aidé, soutenu ou supporté durant la démarche de diagnostic?

    Leave a Reply

  • 2-Quelles ont été vos craintes, difficultés et appréhensions durant la démarche de diagnostic?

    2-Quelles ont été vos craintes, difficultés et appréhensions durant la démarche de diagnostic?

    Témoignage

    2-Quelles ont été vos craintes, difficultés et appréhensions durant la démarche de diagnostic?

    Leave a Reply

  • Inspiring through words: the journey of Jordan Nanos

    Inspiring through words: the journey of Jordan Nanos

    Inspiring through words: the journey of Jordan Nanos

    • 1 avr. 2024
    • 1 min de lecture

    by Patrick Millette and Jordan Nanos

    In a world where the power of words can uplift spirits and spark change, Jordan Nanos stands as a beacon of inspiration. A talented author diagnosed with 22q, Jordan’s story is not just about his diagnosis but also about his resilience, kindness, and unwavering determination to make a positive impact through his writing.

    My story By Jordan Nanos

    Discovering the Passion:

    Jordan’s journey as a writer began when he was a teenager. « I started writing when I was seventeen years old and instantly fell in love with it,” he shares. Writing became a love affair that blossomed quickly, leading him to pen his inaugural book at eighteen. His motivation? “I wrote the book because I wanted to make a change and a difference in the world”. Jordan found happiness in his writing endeavours, which boosted his confidence. “When I write it always gives me a positive attitude because it gives me confidence. My writing makes me believe in myself”. 

    Navigating Challenges with Grace:

    Jordan’s writing journey hasn’t been without its share of obstacles. Yet, with unwavering determination, he has navigated through them with grace and resilience. “I’ve learned that you need to not give up on your writing. I’ve learned that if you believe in yourself anything is possible”. Each challenge became an opportunity for growth, a chance to reaffirm his belief in himself and his craft.

    Jordan strengthened his writing ability through practice and dedication. He found it helpful to discuss his ideas with people around him whenever he wrote. “I would practice at it and face it by having conversations with others. I would make sure what I say makes sense to the other person.” 

    Jordan believes that writing can boost confidence and spread kindness. He hopes to inspire others to pick up the craft. His advice for people who are interested in writing is to “take it one day at a time. Patience is a virtue when it comes to writing. You have to be committed to your writing”. Jordan is an inspiration to many people.

    Spreading Kindness, One Word at a Time:

    Through his books and writings, Jordan Nanos seeks to spread kindness. Throughout his writing, he encourages his readers to approach the world with compassion and understanding. “My writing can help others feel that they’re not alone. It can help others be more thoughtful and helpful towards each other. It can teach others to fight for what’s right when they’re feeling down. It can help to show others that being different is ok”.

    His writing serves as a gentle reminder to others that they’re not alone in their struggles. It encourages empathy, prompts thoughtful gestures, and empowers individuals to stand tall and embrace their uniqueness. ”The message is never to give up. You can always be proud of who you are”. To Jordan Nanos, spreading kindness is vital, and he wants to encourage his readers to spread kindness throughout their lives. “Don’t be shy when you have something to say in a positive way.”

    Jordan wants to inspire others to spread kindness. He does this throughout his books and finds creative ways to spread kindness during special occasions like the holiday season. When you spread kindness through the holiday season you’re showing others that you can do anything that you can put your mindset to. » Throughout the holiday season, Jordan goes out of his way to write Christmas cards for his friends and family. This is a perfect example of utilizing your talents to spread positivity and kindness. For him, spreading kindness during this magical time isn’t just about grand gestures; it’s about embracing the spirit of togetherness, hope, and possibility.

    Beacon of Light:

    In the tapestry of life, Jordan Nanos’s story stands as a vibrant thread, weaving together the essence of resilience, kindness, and the transformative power of words. Through his writing, he invites us to embark on a journey of self-discovery, empathy, and hope. As we navigate through the pages of his life, may we be inspired to embrace our own unique stories, to spread kindness wherever we go, and to believe in the extraordinary potential of the human spirit. Jordan Nanos isn’t just an author; he’s a beacon of light illuminating the path toward a brighter, kinder tomorrow.

  • In other words, I walked right into it.

    In other words, I walked right into it.

    Blog Post by CJ James

    “In other words, I walked right into it.”

    There have been a lot of changes over the last decade of my life, but one constant. I have been a victim of stalking and cyber-harassment (which is just a very specific form of stalking) for the last ten years. It started in Texas with multiple instances of the same man approaching me in person and online. It continued when I moved to Québec, though it is exclusively online for now.

    As an Autistic woman, this stalking has made my life extremely difficult from an organizational and emotions-management standpoint. For about a year, it also made it difficult to get my Vitamin D. Victimhood is not easy for anyone, but I want to explain how being a victim of stalking is even more complicated for an Autistic person. I will explain how these events have affected me personally, illustrate how it affects my relationships to others, and discuss how the solutions that are available in society are not adapted to the needs of Autistic people.

    Need for routine

    One of the first recommendations you will receive when being stalked is to abandon routine and habits. It makes sense. If you use the same path to walk to your car at the same time everyday, then it is easy for someone to learn your routine and insert themselves into it. Same with, say, having a favourite bookstore.

    On the contrary, one of the more famous quirks of Autism is our reliance on routines. We aren’t like this just because we want to be difficult; we need predictability to function. Surprises require more on-the-fly thinking, which is a common challenge for Autistic people. I am no different.

    I need my routine to keep track of my keys, remember to feed my dogs (and myself), and to wake up on time. Without routine, I struggle with the basic-life organization that more normative people call “adulting”. I could not live in an environment where evasion was a daily goal. In the end, it felt like I had the choice between retreating entirely or living with regular, dangerous interruptions due to stalking. I chose to retreat to another country. It gives me room to breathe, but it still negatively affects me –frequently.

    Difficulty reading danger

    Another difficulty that’s somewhat unique for Autistic stalking victims is that reading the danger of a situation is very context-specific and can be confusing. Behaviour that makes sense to an Autistic person can be very dangerous coming from other people. For example, when I was bullied as a child, I kept getting up and repeatedly put myself in situations where I could have been rejected. Over practice (and some help from puberty), I developed the social skills that garnered me a minor, but peaceful social existence. For me, I respect when people try again and again, but in this case, it is not healthy nor respectful. That said, it took me years to recognize that I was being stalked because, to me, he was just trying really hard.

    Another example of this is a lot more harrowing now that I am aware of the connotations. One time, around one in the morning, he confronted me in my apartment complex’s laundromat. For me, I was overwhelmed by the hyper-social nature of Texas social norms, so the surprise that someone was hiding in the dark for me was no different than the stress I experience when someone else is using the laundromat at the same time as me. I just didn’t want to engage in small talk or anything like that. Both situations were annoying in an overwhelming sense, but I had to cope with being overwhelmed all the time.

    Before I even realized that I like being closer to the door than the people around me (I also have PTSD), I had ”played it cool” to the point that I was further into the laundromat than he was, making him closer to the door than me. In other words, I walked right into it. Keep in mind that this is Texas. It’s a violent place and he, later on, threatened my life. What sort of weapons or intentions resided in him? No one knows because, in my attempt to play it cool, I eventually got him talking. I learned that he was there because he was obsessed with me and he was moving away in a few weeks.

    He had envisioned meeting me as a last hurrah. I have no idea what would have happened if I hadn’t pretended to want his number. Certainly he’s so unstable that even he doesn’t know what he intended if I openly blew him off. That said, the danger inherent in a “last hurrah with a woman you’ve been obsessed with for many years” did not occur to me until about a year after I walked out of there. My avoidance for the year after that event was simply my frustration with unexpected social interactions. About the same time I realized the danger I had been in was about a month after he started making unsolicited comments to me about having a gun. I was like a lobster in boiling water.

    Strategies that don’t make sense on first impression

    Another thing that affects stalking victims is that their strategies of stalker-management rarely make sense on first glance. Experts in the field themselves do not agree on how to manage prolonged cyber-harassment, so victims often have to make their own decisions about how they want to manage the threat.

    I have years of evidence of his stalking and harassment due to my strategies, but it’s really hit-or-miss if I am able to explain the methodology to another person. When making my strategy, I just did not care how it looks to other people, so I allowed cyber-harassment on my public posts from a single Facebook account of his for one main reason: the harassment doesn’t stop when I block him and it’s easier to prove all the harassment is coming from the same person if I allow him one account that I do not block.

    I’ve since abandoned this strategy because it was causing social rifts with people perceiving me as “letting it happen” or “wanting it”. Because I am on the spectrum, and because this factoid was public knowledge, people were highly critical of my management strategies, rather than accepting that I had consulted experts and built my own expertise. Ultimately, I just wanted good evidence to put this devil-on-my-back away for a long time and I did not care how other people perceived it.

    Difficulty communicating

    I’ve already hinted at this a little, but stalking is already a difficult crime to communicate because the danger comes from the fact that it’s not a single occurrence. Additionally, there’s some classical conditioning that happens. Not every act of stalking is sinister on its face. However, every act is a reminder that the sinister acts of stalking did happen, could happen again, and might escalate. What a stalking victim feels is not easily communicated.

    …With police

    If you’ve read this far, you’ve probably wondered if I’ve ever contacted the police. There may even be a few comments from people who didn’t finish reading this who are convinced that this would not happen if I had just contacted the police. Sadly, people’s reactions to this crime I experience are becoming more and more predictable to me. However, I did actually try to talk to the police about this crime. A lot.

    There are significant communication differences between what police expect from a victim and what comes out of an Autistic victim. There’s a book and a lot of academic papers about it. In some countries, such as the UK, due to these differences, an Autistic victim can ask for an investigator to report to who is specially trained to communicate with Autistic victims.

    I would love to see something like this in Quebec, as I’ve had mixed experiences reporting my stalker’s activity here. Sometimes they are very understanding, but one time I got dragged out instead of being allowed to report the crime occurring against me. As a result, I have a deal with my éducateur spécialisé where he goes with me to the police station to report my stalker’s more sensational threats.

    I can’t imagine still having this problem in Texas, where I am from. There are no éducateurs/éducatrices spécialisé.e.s in Texas, but they should not be needed anyway. I am lucky that, right now, the stalking behaviour is exclusively cyberharassment, which is Criminal Harassment in Canada, a serious crime punishable by up to 10 years in prison. This lack of urgency, due to the distance, means that I can wait a few days after I receive an especially salient threat for my éducateur spécialisé to be available to go to the police station with me. If the threats were occurring in person, I would not have the time to wait and we would be back to the same problem. For a whole year in Texas, when the stalking escalated to in person contacts, I left my house as little as possible out of fear, cutting me off from sunlight.

    While still in Texas, I tried interacting with the police through a very helpful women’s shelter, but they had no knowledge of Autistic communication so they did not really understand the problem either. It did not help that their funding comes from domestic violence grants and I never dated this man who is stalking me. Autistic crime victims need more than just helpful people, though they do help; we need specialized support when we go to report to the police.

    …With friends and care workers

    There are social challenges in just being an Autistic person, but stalking adds another layer. I often feel like I am on trial as a victim with the people around me such as friends, acquaintances, and care workers. There’s high stakes to strike the right tone with your victimhood/survivourness and absolutely no one to learn it from. This means that minor grievances, such as the way I give walking directions, can transform into full critique of my life, such as the way I manage my victimhood, quite rapidly.

    Everyone has an opinion about how they would handle it if they were you. It’s hard enough to be a victim of a serious crime with heavy psychological effects on my person, but there is an extra layer that comes from people criticizing my decisions, good ones and faults, as everything is under a magnifying glass. This is an extra social challenge to negotiate. No one wants their decisions under a magnifying glass, especially as a result of a crime. As an Autistic person, additional social challenges can feel like an insurmountable mountain. It has been much harder to build my new circle of friends here in Québec as a result.

    Sensory issues and communal shelters

    Lastly, stalking victims are often pushed to start over in the shelter environment. This is because starting over is very spendy, but, even when you’re not disabled, stalking conflicts with generating income. The emotional experience of stalking is another weight on your “adulting” skills and the act of stalking often interferes with employment. Thus, the free shelter enters.

    But there’s a huge caveat. Autistic people can be too sensory sensitive and socially different to survive in communal environments (without other Autistic people).

    While some shelters can place a person in a private room, crowding and understanding are barriers. Most shelters do not recognize the specialized needs of Autistic people well enough to accommodate them. Personally, I could never have started over if I hadn’t been especially good at crowdfunding and then also had some seriously lucky outcomes. One time, when I was a homeless new arrival in Trois Rivières, the CLSC paid for me to stay in a cheap motel for the weekend and then placed me (and my dogs) in supported Autistic housing the following Monday. This was especially lucky because I had nowhere to go, crowdfunding was in a lull, and staying at the only shelter in town was also not an option. One of the many reasons why I volunteer my writing to Autism House is because they are aware of the Autistic community’s specialized housing needs and their goal is to eventually provide it. I think that will save lives we haven’t even heard about yet.

    Overall, stalking is a difficult crime whether or not you are Autistic and this review of our unique challenges as stalking victims is not intended to downplay other stalking victims. It is always hard and there is always someone who has survived worse. Before the 90s, neither stalking nor Autism were widely recognized, but the confluence of the two has some unique traits that, frankly, suck. Every year, both issues gain general awareness in the global zeitgeist. I hope that this work can make a meaningful contribution to both as well. Please share!

  • Un chez soi dans la communauté!

    Un chez soi dans la communauté!

    Un chez soi dans la communauté!

    Les besoins, attentes et préférences d’adultes autistes en matière d’hébergement et de logement au Québec

    • 22 févr. 2023
    • 1 min de lecture

    Dernière mise à jour : 18 juin 2023

    En décembre 2020, le Réseau pour Transformer les Soins en Autisme (RTSA) et la Maison de l’autisme ont organisé une table de concertation intitulée Vers une meilleure qualité de vie pour la communauté adulte autiste : Besoins et services en hébergement. À la suite de cet événement, la Maison de l’autisme s’est jointe aux chercheur.e.s Baudouin Forgeot d’Arc (M.D., Ph. D.) et Isabelle Courcy (Ph. D.) pour créer un partenariat communauté-recherche.

    Le projet né de cette alliance visait à documenter les besoins, les attentes et les préférences des personnes autistes au Québec en matière d’hébergement ou de logement.

    Au cours de 2022, le sondage a été partagé par plus de 150 organisations et rempli par près de 400 personnes à travers le Québec.

    Pour consulter les résultats:

    Télécharger PDF • 990KB

    Pour consulter la couverture médiatique: https://lactualite.com/actualites/trop-peu-de-logements-adaptes-aux-besoins-des-autistes-revele-une-nouvelle-etude/