{"id":617,"date":"2019-08-01T13:43:13","date_gmt":"2019-08-01T03:43:13","guid":{"rendered":"https:\/\/www.downsyndrome.org.au\/voice\/?p=617"},"modified":"2021-02-15T12:26:30","modified_gmt":"2021-02-15T01:26:30","slug":"book-review-portrait-of-the-artists-mother-by-fiona-place","status":"publish","type":"post","link":"https:\/\/www.downsyndrome.org.au\/voice\/2019\/08\/01\/book-review-portrait-of-the-artists-mother-by-fiona-place\/","title":{"rendered":"Book review – Portrait of the Artist’s Mother by Fiona Place"},"content":{"rendered":"\n
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\"Fiona<\/figure>\n<\/div>\n\n\n\n
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In the print journal we ran a review from Jackie Softly of the fabulous book Portrait of the Artist\u2019s Mother <\/em> by Fiona Place. This book was so popular that we received an extra review! <\/p>\n\n\n\n

Place,F. (2019) Portrait of The Artist\u2019s Mother<\/em>, Spinifex Press, Australia.<\/p>\n\n\n\n

You can purchase the book through Spinifex Press<\/a><\/p>\n<\/div>\n<\/div>\n\n\n\n

Read both reviews below: <\/p>\n\n\n\n

Review by Jackie Softly<\/h2>\n\n\n\n

Fiona Place is a national-award-winning writer and poet, a mother and an advocate for people with intellectual disabilities. In Portrait of the Artist\u2019s Mother<\/em>, she writes about her experience as mother to a son with Down syndrome in today\u2019s Australia. Her son, Fraser Pollock (23), is an acclaimed visual artist. <\/p>\n\n\n\n

Portrait<\/em>, ten years in the writing, takes readers from Place\u2019s pregnancy with Fraser and through his life so far. Portrait<\/em>, is far removed from anything I\u2019ve read on parenting children with Down syndrome before. Described as \u2018one of our great truth tellers\u2019 and as writing \u2018glorious prose\u2019, Place\u2019s turn of phrase is why this book is so compelling. <\/p>\n\n\n\n

Portrait<\/em> is far more than the story of one person, one mother and one family. While we get to share in this family\u2019s often hilarious and sometimes terrifying child-rearing experiences, the book explores motherhood and what this means when you have a disabled child in today\u2019s society.  <\/p>\n\n\n\n

Place has produced a work with a number of layers, beautifully executed to create the final portrait. Fraser is always at the heart of the book, but Place also explores her family history and her personal experiences to understand their influence on her approach to motherhood and attitudes about disability. Her family\u2019s history, the characters, the reminiscences, the family\u2019s secrets laid bare and Place\u2019s own family relationships and her experience as a young paediatric nurse, come to life on the page in beautiful storytelling. <\/p>\n\n\n\n

Another crucial layer to this book explores why today\u2019s society sees people with intellectual disabilities as less worthy of life, as people not wanted, needed or welcomed. <\/p>\n\n\n\n

Place skilfully shows how the terrible history and politics of disability still influence modern-day Australia, explaining why a society that claims to welcome diversity chooses termination of babies with Down syndrome at a stunningly high rate, and excludes more children with intellectual disabilities from regular schools than it did 20 years ago. <\/p>\n\n\n\n

In all the layers of Portrait of the Artist\u2019s Mother<\/em>, there is a fundamental truth; if we want to understand the present, we need to see where we have come from. Fiona Place has done this with courage, honesty, passion for change and clearly, much love. Portrait <\/em>is rich, raw and complex but immensely readable.  I have highlighted so many passages and am bursting to read them out loud to anyone!<\/p>\n\n\n\n

Portrait of the Artist\u2019s Mother<\/em> has enormous potential to bring about change. As a mother, I want to share this book with all parents of children with disabilities, so they can understand why they and their children are treated as they are, and know how to create change.<\/p>\n\n\n\n

Portrait <\/em>should be read and shared far and wide; not only with parents, but on school and university curriculum and on reading lists for health and allied health professionals, educators, service providers and community decision makers. <\/p>\n\n\n\n

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Review by Margaret Booker<\/h2>\n\n\n\n

Fiona and I are parents of young adult sons with Down syndrome. Our experiences of raising our sons in the Eastern suburbs of Sydney have overlapped for more than two decades. Reading Fiona\u2019s memoir brought my experiences in all their lows and hard-won highs rushing back. <\/p>\n\n\n\n

From the early fights to have our sons recognised as being entitled to mainstream services. Neither of us were \u2018allowed\u2019 to enrol our sons in mainstream public education; I can still visualise every detail of the room in which the Principal of the school first \u2018appealed to my understanding\u2019 then firmly ushered me out (her time being wasted). My shock and sadness as I registered my son and I were beyond the pale. <\/p>\n\n\n\n

Fiona\u2019s insight in to how this outsider status impacted on us over the years is startling. How we, because of our love for our sons, haven\u2019t felt entitled to lament what we have sacrificed of our own lives. Friends fall away (tired of our attempts at justifying, long after the toddler years why we still can\u2019t reliably commit to social engagements) our careers are never what we had hoped for. And we feel tired, a different tired.  <\/p>\n\n\n\n

Fiona looks back now at the true cost of her son\u2019s education (the only school offering mainstream); an expensive independent school. The ripples and waves impacting the rest of Fiona\u2019s family are felt. <\/p>\n\n\n\n

This book has so much more. Fiona writes like her son Fraser paints; Sydney and it\u2019s history come alive.  Please look at Fraser Pollocks work on https:\/\/fraserpollock.wordpress<\/a>. Fiona\u2019s visual descriptions of Sydney meant I enjoyed locating them in my own mind and felt myself back in a Sydney through seven generations of one extraordinary family. I was a witness to the complex grief of her own immediate family\u2019s tragedies. <\/p>\n\n\n\n

We also see the changing (and remarkably fixed) attitudes and ideas about disability. We are brought into how these ideas are to help us with our new challenges of the NDIS. I want Fiona to keep writing her and Fraser\u2019s life story, as our challenges are always exceptional. <\/p>\n\n\n\n

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Have you read it?<\/h2>\n\n\n\n

Comment below and give us your review<\/p>\n\n\n\n

Or get in touch to review another book you like<\/p>\n\n\n\n

SHARE YOUR STORY<\/a><\/div>\n<\/div><\/div>\n","protected":false},"excerpt":{"rendered":"

In the print journal we ran a review from Jackie Softly of the fabulous book Portrait of the Artist\u2019s Mother […]<\/p>\n","protected":false},"author":1,"featured_media":633,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","inline_featured_image":false,"footnotes":"","_links_to":"","_links_to_target":""},"categories":[1],"tags":[],"class_list":["post-617","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"_links":{"self":[{"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/posts\/617","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/comments?post=617"}],"version-history":[{"count":5,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/posts\/617\/revisions"}],"predecessor-version":[{"id":1039,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/posts\/617\/revisions\/1039"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/media\/633"}],"wp:attachment":[{"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/media?parent=617"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/categories?post=617"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.downsyndrome.org.au\/voice\/wp-json\/wp\/v2\/tags?post=617"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}