Disability Portraits from Brazil
https://www.retratosdeficas.com/
Disability Anthromom. My writings my own.
Occupying Disability: Critical Approaches to Community, Justice, and Decolonizing Disability
Block, P., Kasnitz, D., Nishida, A., Pollard, N. (eds). Springer Ltd.
Allies and Obstacles: Disability Activism and Parents of Children with Disabilities
Allison C. Carey, Pamela Block, and Richard K. Scotch, Temple University Press (book talk and panel discussion here)
Block, P., Ellison E., Squillace, M. (2017) VENTure Think Tank: The politics, technologies, and occupations of disability and mechanical ventilation. In Occupational Therapy without Borders: Integrating Justice into Practice, Elsevier, Cambridge, UK.
https://evolve.elsevier.com/cs/product/9780702059209?role=student
Lima, RC, Evans, C, Feldman, C, and Block, P (2018) Autism Policy and Advocacy in Brazil and the United States. IN Fein, E and Rios, C. Autism in Translation: A Cross-Cultural Conversation Regarding Autism Spectrum Conditions. New York: Palgrave.
Patterson, S & Block, P. (2019) Disability Vulnerability and Capacity to Consent. IN Cascio A. and Racine E. Research Involving Participants with Impaired Cognition: Ethics, Autonomy, Inclusion, and Innovation. Oxford, England: Oxford University Press.
https://www.oxfordscholarship.com/view/10.1093/oso/9780198824343.001.0001/oso-9780198824343
1. Block, P. 2020 Esterilizacao e Controle Sexual. In (Eds. D. Allebrandt, N. E. Meinerz, P.G. Nascimento) Desigualidades e Politicas da Ciencia. Forianopolis: Casa Verde. https://www.ufrgs.br/redecovid19humanidades/_files/view.php/download/pasta/6/5fa55861c47cc.pdf
Evans, C., Milazzo, M. and Block, P. (2020) “Re-Thinking Disability Community: Chosen and Ascribed Communities or Intersecting Communities and Communities in Conflict.” In (Ed. Bettina Jansen) Rethinking Community Towards Transdisciplinary Community Research. New York: Palgrave.
https://link.springer.com/chapter/10.1007/978-3-030-31073-8_9
Karp, P. & Block, P. (2021) We Float Together: Immersing OT Students in the Salamander Project. In Occupation Based Social Inclusion. (Eds. Brueggen, H., Kantartzis, S., and Pollard, N. Whiting and Birch, London, UK.
http://www.whitingbirch.net/cgi-bin/indexer?product=9781861776051
Ramawati, D., Block, P. (2021). Sexuality and Sexual Rights of Young Adults with Intellectual Disability in Central Java, Indonesia. Routledge Handbook of Disability and Sexuality. New York: Routledge.
https://www.taylorfrancis.com/chapters/edit/10.4324/9780429489570-19/sexuality-sexual-rights-young-adults-intellectual-disability-central-java-indonesia-dian-ramawati-pamela-block
Gesser, M, Block, P, & Leite, LP. (2023). Do capacitismo ao acesso coletivo no ensino superior. In: Sandra Eli Sartoreto de Oliveira Martins e Ana Paula Camilo Ciantelli (Orgs.). Inclusão e Acessibilidade na Educação Superior: desafios atuais, vol. 1. Cultura Academica Editora.pp.79-109.
https://www.mpma.mp.br/arquivos/CAOPID/publicacoes/14609_livro-estudos-sobre-deficiencia-2020.pdf
Angelucci, B.,
Costa, L., Block, P. (2017) People with Disabilities: Fighting for their
Rights in the USA and Brazil. Revista de
Educação PUC-Campinas 22(3): 339-355.
https://www.redalyc.org/journal/5720/572063482002/html/
Kuppers, P. with Johnson, K., Block, P., Preston, VK (2019). Water Work in Play: Public Intimacies. Canadian Journal of Disability Studies 8(1): 32-57.
https://cjds.uwaterloo.ca/index.php/cjds/article/view/470
Pollard, N, Block, P (2017) Who Occupies Disability? Cadernos Brasileira de Terapia Ocupacional, São Carlos 25(2):417-26.
https://shura.shu.ac.uk/16067/2/Pollard%20Who%20occupies%20disability.pdf
Carey, A., Block, P., Scotch R. (2019). Sometimes Allies: Parent-Led Disability Organizations and Social Movements. Disability Studies Quarterly. 39(1): http://dsq-sds.org/article/view/6281/5183
http://dsq-sds.org/article/view/6281/5183
Scarlatos, L., Engoron, E., Block, P., Evans C.
(2019). All Together Now: A Collaborative Game to Increase Advocacy Among
Disabled Individuals in Higher Education. International Journal of Blended and
Mobile Technology 11(4)
https://www3.cs.stonybrook.edu/~lori/pubs/LLS2017_AllTogetherNow.pdf
https://disabilityglobalsouth.files.wordpress.com/2019/07/06_02_05.pdf
In Spanish:
Gesser, M., Block P., and Mello A.G. (2022) Estudios sobre discapacidad: interseccionalidad, anticapacitismo y emancipación social. Andamios 19(49).
https://andamios.uacm.edu.mx/index.php/andamios/article/view/924/pdf
And in Portuguese:
1.
Gesser, M., Block P. Mello A.
(2021). Estudos da
deficiência: interseccionalidade, anticapacitismo e emancipação social. In
(Eds. Gesser, M; Böck, G & Lopes, P. H.) Estudos da Deficiência:
anticapacitismo e emancipação social [Disability Studies: Anti-ableism and
social emancipation]. Florianópolis: CVC.
Karp, P. and Block, P.(2022). Float to Grow:
Nurturing the Roots of Socially Inclusive and Just Practice in Occupational
Therapy Students. Brazilian Journal of Occupational Therapy.
https://www.scielo.br/j/cadbto/a/f4xHFzLLN8d9bd4dsXtvbHf/abstract/?lang=en
Alumukhtara, A., Johnstone, L. DePasquale, R., Warren, N., and Block, P. (2022) Aging with (and into) Assistive Technology: An exploration of the narratives of amputees and polio survivors. Disability and Rehabilitation: Assistive Technology
https://www.tandfonline.com/doi/abs/10.1080/17483107.2022.2131916
https://www.emerald.com/insight/content/doi/10.1108/S1479-354720230000013007/full/html?skipTracking=true
https://www.tandfonline.com/doi/full/10.1080/17458927.2022.2138090
Aging
Sisters: Health, Communication, and Care
Pamela
Block, March 2023
I’ve decided to talk about my North American
research on care relationships between disabled people and their families with
particular focus on the intersectional experiences of two women, one autistic
and one with ADHD: my sister Hope, and myself. We are two aging women in our
mid-50s 15 months apart in age, we grew up together. I am a disability
anthropologist and my most recent coauthored book looked at the relationships
between social movements run by parents of disabled people and those led by disabled
activists (Carey, Block, Scotch 2020). I have a newer project looking
specifically at the care relationships between siblings with the specific goal of
disrupting the typical narratives of what a “caregiver burden” disabled people
are to their families (Block et al. 2022). Hope shares a house with another
disabled woman in Southern Rhode Island. She likes to cook, go out for coffee, do
crafts, care for horses, to do shredding, to look at pictures, to watch her TV
shows, and to travel.
This is one of a series of essays on the lived
experiences I share with my sister Hope, who is autistic, and our mother,
Barbara, who spent her life in alliance with my sister in disability and
autistic activism (Block, Block, and Kilcup 2008, 2009; Block et al. 2012). The
two of them worked together to draw me into activism and collaborative autoethnographic
scholarship on autism, communication, and family beginning in 2008, most of
these essays available on my blogspot. There is also a film made with the
Restorying Autism Project (Block with Block, Lebo and Lebo 2016).
As I wrote the first draft of this presentation
in late February 2023 it was in the context of a lit candle, a yahrzeit candle
for our mother, who died of cancer 10 years ago. Hope and I now live in
different countries. Hope’s services and supports where she lives in the US are
far better than she could ever get in Canada, even if she were allowed to
immigrate – which would be unlikely due to the eugenics era policies that
prevent entry of people considered burdens on the state. Hope prefers to live
in Rhode Island and has reminded me that I am not her guardian, and she is
happy living her own life in Rhode Island. This has meant that we see each
other rarely, and of course the Covid-19 pandemic made visiting even more
complicated. I never imagined on moving to Canada in 2019 that there would be a
closed border between us.
It is an unhappy coincidence that my sister and
I have both, during this period of our mother’s yahrzeit, been drawn into what
I will optimistically characterize as mild cancer scares, we both have bodily
anomalies, that are almost certainly not cancerous, although no doctor will
definitively say that. In any case, both of us have bodily anomalies that
require further investigation: my sister an ovarian cyst and me tiny cysts in
one of my breasts. My sister is non-speaking, and to many people that means she
is incapable of making complex decisions or communicating in complex ways, but
we have found this to be untrue. Hope is quite perceptive and intelligent, and she
has found many ways to communicate without using spoken speech. She uses her
body. She uses personal sign language and facial expressions, and she uses her
voice through hums that express her emotional state. She is a master of
physical humor and nuanced facial expressions. Though it is not her preferred
way of communicating, she can also do some assisted typing. Supported typing is
considered problematic because of the perceived potential for manipulation and
abuse. However, new technologies such as tracking eye gaze and developments in
thought-based communication are starting to advance to a place where these
concerns can be addressed more definitively (Jaswal et al. 2020, Willett et al.
preprint). Despite all the controversy Hope has occasionally used this method
of communication in rather mundane and unproblematic ways for almost 30 years
now.
A few weeks ago, I was pulled out of one of my classes
repeatedly due to doctors calling me. Her doctor and mine. I had requested to
be included in Hope’s appointment with her radiologist/oncologist to discuss
Hope’s cyst and coincidentally the breast care center called to reschedule my
biopsy (update: when I went to get the biopsy I found out the procedure was cancelled because on looking at previous mammograms they determined there was no need). The doctor for Hope says her cyst is almost certainly not cancerous: “I’ll
never say never, but there’s no indication that this is in any way cancerous,
but it’s the size of an orange and many women would request that it be removed.”
However, she noted that there are risks in surgery and Hope has some medically
and neurologically complex issues that make surgery riskier. So, we could just
monitor it, but not try to remove it. That is what the doctor seemed to be
leaning toward and I was leaning that way as well, but with doubts. The woman
who took Hope to the appointment happens coincidentally to also be one of the
few people left alive who has been trained to type with Hope but her job is to
ferry people to medical appointments and so she has very little time to do this
anymore. On this day she had to rush Hope back home after her appointment and did
not have a chance to type with her, but she and I chatted over the weekend and
we both decided it was very important that Hope have the chance to type about
her options and to do it while in a contact with a nurse who could answer all
her questions.
So, I immediately went on a quest to make that
possible, knowing that there are a lot of barriers, both structural and
interpersonal barriers because by insisting that this happen, I stress out her
staff, annoy the administration of the agency, and I inconvenience our friend,
Linda, who types with Hope. Linda lives in another state and has a husband who
has a lot of medical issues, making it hard for her to connect with Hope. In
fact, it has been years, our last meeting was pre-pandemic lockdown in February
2020. And I am skimming over the logistics but it did involve a lot of
negotiation and stress for a lot of people, but we persevere dand Hope and her
staff person drove for an hour and Linda drove an hour and they met halfway
between so that the two of them could type together. It turns out that Hope
adamantly wanted the cyst removed even if it’s not cancerous because she
remembered the cancer growing inside of our mother and the terrible pain that
she was in. Hope does not want to die experiencing that kind of pain. The nurse,
who attended the meeting by phone started crying and telling her the agency would
support her wishes. Hope’s staff person discussed the possibility of trying to
arrange for Hope and Linda to meet monthly. But Linda goes home to discover
that her husband, who had that morning been perfectly fine, now had some new
onset medical issues making that plan difficult.
These are the complex relations of care between
two aging sisters facilitated by paid and unpaid caregivers across communication
barriers, distance, and time. My understanding of care relationships is
influenced by Eva Kittay (1999, 2019), whose daughter has very high support
needs and no verbal communication. Kittay developed her theory of care in a
context of a philosophical landscape where people like her daughter were
compared to animals and so-called “compassionate killing” deemed appropriate.
But Kittay talks about the value generated by dependence on others, and the
value to a society for caring for dependent individuals. There is value in
humans caring for each other, whether it’s mothers for children, sisters for
sister, or formal or informal networks for caring for people within a society. I
am also very influenced by understandings of care articulated by disability
justice scholars and activists (Nishida 2022, Piepzna-Samarasinha 2018, 2022, Wong 2022).
Written by and for disabled queer people of color, these are strategies for
survival in a world of systemic racism, structural violence, pandemics, and
environmental disaster. Using Fine and Glendinning’s (2005) discussion of how
humans experience dependence, interdependence and so-called independence, I
know that independence -- whether it’s independent communication or independent
living -- is an illusion and that all of us experience interdependence and
dependence throughout out lives. In the context of this recent experience, I am
revaluing and reassessing what exactly dependency means. There is value in
being dependent on others, and caring for others who are dependent. Looking at
my and my sister’s lives and the webs of relationships that sustain us, I am
awed by the complexity of the care relationships that allow us to more than
live, but to dream, communicate, connect, to have goals, wishes, and dreams and
to sometimes have these honored and fulfilled.
References
Block, P., Block H., Kilcup B. (2008) Autism,
Communication and Family. https://pamelablock.blogspot.com/2015/10/autism-communication-and-family.html
Block, P., Block, H., Kilcup B. (2009). Bus
Rides and Back Rooms: Autism, Family, Meaningful Occupation & Life
Transition. https://pamelablock.blogspot.com/2015/10/autism-communication-and-family.html
Block, P., Shuttleworth, R. Pratt, J., Block,
H., Rammler, L. (2012) Disability, Sexuality and Intimacy. IN Politics of
Occupation-Centered Practice: Reflections on Occupational Engagement Across
Cultures. (Eds. Pollard, N., Sakellariou, D.). Oxford, England: Elsevier
Churchill Livingstone.
Block, P. with Block, H., Lebo, S. and Lebo I. (2016)
Hope’s Story. https://www.restoryingautism.com/allies-and-obstacles
Block, P., McKinley G. (2022), Care
Relationships of Adult Disabled and Nondisabled Siblings, SSHRC Partnership
Engage with match from Azrieli Foundation Centre for Caregiving Excellence.
CAD$55,000 September 2022-August 2023.
Carey, A., Block, P., and Scotch R. (2020).
Allies and Obstacles: Parents of Children with Disabilities and Disability
Rights. Philadelphia, PA: Temple University Press.
Jaswal
VK, Wayne A, Golino H. Eye-tracking reveals agency in assisted autistic
communication. Sci Rep. 2020 May 12;10(1):7882. doi:
10.1038/s41598-020-64553-9. PMID: 32398782; PMCID: PMC7217901.
Fine,
M. & Glendinning, C. (2005). Dependence, independence or inter-dependence?
Revisiting the concepts of ‘care’ and ‘dependency.’ Ageing & Society
25:601–621
Kittay,
E. F. 1999. Love’s Labor: Essays on Women, Equality, and Dependency. Routledge,
New York.
Kittay,
E. F. 2019. Learning from My Daughter: The Value and Care of Disabled Minds. Oxford
University Press. New York.
Nishida,
A. (2022) Just Care. Temple University Press. Philadelphia.
Piepzna-Samarasinha,
L. L. (2018). Care Work: Dreaming Disability Justice. Arsenal Pulp Press.
Piepzna-Samarasinha,
L. L. (2022). The Future is Disabled. Arsenal Pulp Press.
Willett, F., Kunz, E., Fan, C., Avansino, D., Wilson,
G., Choi, E. Y., Kamdar, F., Hochberg, S. D., Shenoy K. V., Henderson, J.M.
(preprint) A high-performance speech neuroprosthesis. https://www.biorxiv.org/content/10.1101/2023.01.21.524489v1.full.pdf+html
Wong, A. (2022) Year of the Tiger. Penguin Random House.