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LoveQuiltsUK - Maisie M's quilt

Maisie M's quilt    (Quilt Completed)

Born:2007
Illness: Pyruvate kinase deficiency, blood transfusion dependent, no spleen, iron overload.

Theme: Enchanted World

Quilt delivered: 24th Mar 2023
Photo of Maisie M

Thank you

Coming soon...



Finished photos

Coming soon...


Quilted by: Alison and Janine

Individual squares

Cross stitch square for Maisie M's quilt
Stitched by: Anne (+)
Submitted: Jan 2023

Cross stitch square for Maisie M's quilt
Stitched by: Gemma Boreham (+)
Submitted: Nov 2022

Cross stitch square for Maisie M's quilt
Stitched by: Jan G (+)
Submitted: Jan 2023

Cross stitch square for Maisie M's quilt
Stitched by: Jan S (+)
Submitted: Dec 2018

Cross stitch square for Maisie M's quilt
Stitched by: Jan S (+)
Submitted: Jan 2023

Cross stitch square for Maisie M's quilt
Stitched by: Jodi Maple (+)
Submitted: Jan 2023

Cross stitch square for Maisie M's quilt
Stitched by: Julie (+)
Submitted: Jan 2023

Cross stitch square for Maisie M's quilt
Stitched by: Kaz Bowen (+)
Submitted: Dec 2022

Cross stitch square for Maisie M's quilt
Stitched by: Miss Debbie Elkington (+)
Submitted: Nov 2022

Cross stitch square for Maisie M's quilt
Stitched by: Nicky (+)
Submitted: Jan 2023

Cross stitch square for Maisie M's quilt
Stitched by: Pru (+)
Submitted: Nov 2022

Cross stitch square for Maisie M's quilt
Stitched by: Sue (+)
Submitted: Dec 2022


Card

Card for Maisie M
Stitched by: Jan Garton

Biography

Maisie was ventilated at birth. She received 3 blood transfusions in her first day of life, her jaundice levels were 700 (usually 45). Maisie continued to receive blood transfusions every 3 weeks due to her haemoglobin dropping drastically.

Maisie has many operations including a Hickman line and Portercath inserted into her chest and 2 bone marrow aspirations. Maisie has had a total of 150 blood transfusions to date. She has also had her spleen and gall bladder removed.

Maisie is the 40th person in the UK to be diagnosed with pyruvate kinase deficiency. The illness is so rare that it took doctors 14 months to find a diagnosis.


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