{"id":285,"date":"2021-05-20T09:53:00","date_gmt":"2021-05-20T08:53:00","guid":{"rendered":"https:\/\/www.sense.org.uk\/?p=285"},"modified":"2023-04-20T09:54:27","modified_gmt":"2023-04-20T08:54:27","slug":"our-daughter-has-a-rare-chromosome-disorder-finding-sense-was-the-best-thing-we-did","status":"publish","type":"post","link":"https:\/\/www.sense.org.uk\/blog\/our-daughter-has-a-rare-chromosome-disorder-finding-sense-was-the-best-thing-we-did\/","title":{"rendered":"Our daughter has a rare chromosome disorder \u2013 finding Sense was the best thing we did"},"content":{"rendered":"\n

Six-year-old Tilly is supported by Sense, and has a rare chromosome disorder causing poor vision, hearing loss and learning difficulties. Her mum, Louise, explains how Sense have supported Tilly and her family during lockdown. <\/p>\n\n\n\n

When Tilly was three months old, a paediatrician noticed she hadn\u2019t reached some of her milestones. After running some tests, the hospital told us that she has a rare chromosome disorder, as well as having very poor vision. By the time Tilly was three years old, she was also diagnosed with some hearing loss.  <\/p>\n\n\n\n

It was around this time that we started going to sessions at the Sense Woodside Family Centre. We were still taking Tilly to a baby sensory group and was looking for other groups for older children, where she could get the sensory stimulation she loved.  <\/p>\n\n\n\n

I was quite nervous about reaching out and meeting other people, but honestly, it\u2019s the best thing we did. I wish I\u2019d gone before. Once I plucked up the courage to go to Sense Woodside we just haven\u2019t looked back. <\/p>\n\n\n\n

Sense Woodside supported Tilly to develop <\/h2>\n\n\n\n

When we first started going to Sense Woodside as a family, Tilly wasn\u2019t able to participate in the sessions, and she loved lying on the floor and looking at the bright lights. But going to the sessions had such a positive impact on us as a family because we suddenly found ourselves with people who knew what we were going through.<\/p>\n\n\n\n

It\u2019s been amazing to work with the Sense team to develop Tilly\u2019s communication. Before, she couldn\u2019t communicate with us but Caitlin, a Sense Children and Family Support Worker, is supporting Tilly to learn to sign. <\/p>\n\n\n\n

Nowadays Tilly is very playful, she\u2019s got such a bubbly, friendly personality. She likes throwing balls and watching them roll down things, anything with movement really. And she loves music.<\/p>\n\n\n\n

\"A<\/figure>\n\n\n\n

During the pandemic, we carried on taking part online <\/h2>\n\n\n\n

When the first lockdown was announced last year, I was really worried. I just didn\u2019t know how it would impact on us as a family, what the impact would be on Tilly and her health, and I was worried about feeling isolated. <\/p>\n\n\n\n

During the pandemic we\u2019ve carried on taking part in Sense family sessions online. At first it was difficult for Tilly to engage with online sessions, but she soon became used to her new routine and now loves taking part in the songs. <\/p>\n\n\n\n

Nursey rhymes like Wheels on the Bus and Wind the Bobbin Up are two of her favourites. Each session the team sing a welcome song to each child, and Tilly gets very excited and uses the \u2018T\u2019 sign to introduce herself. <\/p>\n\n\n\n

We were also sent some craft kits at Christmas which were brilliant, as well as some sensory toys. It\u2019s great to have something for Tilly to smell or touch to get all her senses involved. <\/p>\n\n\n\n

Sense has helped us to keep connected to other families during the pandemic. The team have supported Tilly to keep connected with her friends. Just knowing that the support is there and that we can join in at any point is so helpful. <\/p>\n","protected":false},"excerpt":{"rendered":"

Six-year-old Tilly is supported by Sense, and has a rare chromosome disorder causing poor vision, hearing loss and learning difficulties. <\/p>\n","protected":false},"author":15,"featured_media":286,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_acf_changed":false,"_searchwp_excluded":"","footnotes":""},"categories":[7],"tags":[],"display_author":[128],"class_list":["post-285","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-blog","display_author-louise-tillys-mum"],"acf":[],"_links":{"self":[{"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/posts\/285","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/users\/15"}],"replies":[{"embeddable":true,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/comments?post=285"}],"version-history":[{"count":0,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/posts\/285\/revisions"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/media\/286"}],"wp:attachment":[{"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/media?parent=285"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/categories?post=285"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/tags?post=285"},{"taxonomy":"display_author","embeddable":true,"href":"https:\/\/www.sense.org.uk\/wp-json\/wp\/v2\/display_author?post=285"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}