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Top News In மான்செஸ்டர் அரச குழந்தைகள் Today - Breaking & Trending Today

Brave girl may get potentially life-changing drug after parents mount successful legal challenge


Brave girl may get potentially life-changing drug after family mounts successful legal challenge
Fifi is such a brave girl and we are all so proud of how she gets on with life and stays so positive despite her deteriorating condition.
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Sale mum's quest after discovering reason for daughter's weight loss


Paola Gallardo with Sonia and Sonia s dad Ivan
A MUM from Sale in Greater Manchester, is raising money for Brain Tumour Research, in support of her three-year-old daughter, who is living with a brain tumour. 
Paola Gallardo, 35, is taking on the 10,000 Steps a Day in February Challenge to raise vital funds for the charity. It’s after her daughter Sonia was diagnosed with a brain tumour in August 2019, following months of tests to try to find
the cause of her unexplained weight loss.
Full-time-mum Paola, said: “Sonia was nearly 18 months old when we noticed she was losing weight. She weighed 10 kilos at 12 months but six months later she’d dropped to nine kilos. We saw the GP, who thought it was because she was beginning ....

Greater Manchester , United Kingdom General , United Kingdom , City Of , Ivan Aparicio , Matthew Price , Paola Gallardo , Facebook Group , Brain Tumour Research , February Challenge , Trafford General , Manchester Royal Children , Brain Tumour , Tumour Research , அதிகமானது மான்செஸ்டர் , ஒன்றுபட்டது கிஂக்டம் ஜநரல் , ஒன்றுபட்டது கிஂக்டம் , நகரம் ஆஃப் , இவன் அபரிசீவ் , மேத்யூ ப்ரைஸ் , பாலா கால்டொ , முகநூல் குழு , மூளை கட்டி ஆராய்ச்சி , பிப்ரவரி சவால் , டிராஃபோர்ட் ஜநரல் , மான்செஸ்டர் அரச குழந்தைகள் ,

Little Ella's weight loss baffled doctors for months - now her family want to raise awareness of a condition 'no one has ever heard of'


Little Ella s weight loss baffled doctors for months - now her family want to raise awareness of a condition no one has ever heard of
Ella Cooper was diagnosed with Wiedemann–Steiner syndrome at 22-months-old
Ella Cooper (Image: Kay Garratt)
The parents of a little girl who wasn t putting on weight due to a rare genetic syndrome now want to raise awareness after her diagnosis.
Ella Cooper stopped breathing after she was born at Tameside Hospital on New Year s Day 2019.
Her mum Kay Garratt, 38, said she was then never very well as a baby, with doctors first believing that she had a dairy allergy. ....

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"When there are options, there is hope" - mum is raising money so scientists can learn more about the brain tumour affecting her three-year-old daughter


“When there are options, there is hope” - mum is raising money so scientists can learn more about the brain tumour affecting her three-year-old daughter
Sonia Gallardo has undergone a number of treatments after being diagnosed with a brain tumour in August 2019.
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United Kingdom , City Of , Ivan Aparicio , Matthew Price , Sonia Gallardo , Paola Gallardo , Facebook Group , Brain Tumour Research , Manchester Evening News , Brain Tumour , Trafford General , Manchester Royal Children , February Challenge , Greater Manchester News , ஒன்றுபட்டது கிஂக்டம் , நகரம் ஆஃப் , இவன் அபரிசீவ் , மேத்யூ ப்ரைஸ் , சோனியா கால்டொ , பாலா கால்டொ , முகநூல் குழு , மூளை கட்டி ஆராய்ச்சி , மான்செஸ்டர் சாயங்காலம் செய்தி , மூளை கட்டி , டிராஃபோர்ட் ஜநரல் , மான்செஸ்டர் அரச குழந்தைகள் ,