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Coraline & Us

Article for "Wouldn't Change a Thing"

 
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My piece written for Wouldn't Change a Thing. Delighted to be featured by them.

Read the article here: Belief

 
Awareness, Awards, Lockdown, Values, Coraleen SkincareLizNovember 20, 2020
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Useful Links

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Down's Syndrome Association

Canadian Down's Syndrome Society

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View fullsize I’ve joined a group of mums to answer a Monday question. . Today’s is: “What is your child like personality-wise?” . I have written before about when I asked my dad, “but why would people like me?” (at a time when
View fullsize I found these pictures yesterday by chance when looking for some photos of Coraline when she was younger, for a guest post I was writing. . They are from mid November 2018 when we took Coraline back for a check-up after her open heart surgery earlier
View fullsize Kev has been taking some beautiful pictures of Coraline lately. . We thought, as it’s Father’s Day tomorrow, that Kev could take the floor on here and answer any questions you have for him over the next couple of days. See our stories. .
View fullsize I thought I’d post this which I wrote a while back. . A conversation yesterday (about the importance of accepting all emotions, and allowing and honouring them, as then they move through) reminded me of it. . When Coraline was born I was in sho
View fullsize Post 2 of 2 on feeding: . Coraline has sweet potatoes, sardines, kale, curry, scallops, prawns, this kind of thing. . She vary rarely has pasta and has hardly ever had bread. Some parents of children with Down’s syndrome have told us that glute
View fullsize I’ve joined a group of mums to answer a Monday question. Today’s is: . “Tell us about your feeding journey with your child with special educational needs. Did you have to take anything particular into account?" . I have loads
View fullsize I love this picture which Kevin took yesterday morning. Coraline is in her new giraffe T-shirt. . I was singing nursery rhymes and Coraline was joining in on some of the actions to them which she loves to do. . As Coraline is not yet talking we know
View fullsize I’ve joined a group of mums to answer a Monday question. This week’s is: . “Do you take notes when your child has appointments? Do you do extra research too?” . Yes! I take notes! They are almost verbatim notes! Those kind of
View fullsize After Coraline was born and thereafter, I was looking for books written by parents of children with Down’s syndrome. I suppose it’s a bit like an internet search, you keep looking until you find what you want to hear. . I would think to m
View fullsize I have shoeboxes for each year since August 2017, the summer Coraline was born. . I put in little treasured items, postcards from friends, or news clippings from that year. . In 2017’s box there are all the amazing cards we received when Corali
View fullsize I’ve joined a group of mums to answer a question on a Monday. Today’s question is: . “Are you taking any special precautions for your child with special educational needs during Covid 19?” . We are doing the usual; staying hom
View fullsize I love how much passion, thought and care Kevin takes over Coraline’s food. . Today’s al fresco lunch he prepared for her: Courgette ribbons with lemon, parmesan, truffle and pistachios. . #toddlerlife #toddlerfood #downsyndrome #downsynd
View fullsize I’ve joined a group of mums to answer a Monday quesion. This week’s is: . “When deciding on school, day care or a carer for your child with special needs, what type of things do you take into account?” . For us, it’s abo
View fullsize I couldn’t choose my favourite picture, so here they all are. Hair transition by Kevin.
View fullsize I find that I am noticing more after 9 and a half weeks in lockdown. Are you noticing more? . When I take Coraline for a walk I look out for the flowers, and the blossoms, and I stand close and marvel at their colour and design. They bring me wonder
View fullsize

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