S L R . P H O T O G R A P H Y

S L R . P H O T O G R A P H Y A self-taught photographer

Elise & Philips Gender Reveal
15/06/2023

Elise & Philips Gender Reveal

Leah's Photoshoot
26/07/2022

Leah's Photoshoot

Maisie’s African Themed Photoshoot
22/05/2022

Maisie’s African Themed Photoshoot

Maisie’s Ballet Photoshoot
22/05/2022

Maisie’s Ballet Photoshoot

Nellie’s Newborn Photoshoot
22/05/2022

Nellie’s Newborn Photoshoot

The Mcaleavy Wedding
22/05/2022

The Mcaleavy Wedding

The Ward Wedding
22/05/2022

The Ward Wedding

After reading Harper’s story, we decided to get in touch with her parents to offer them a free photoshoot of their beaut...
22/05/2022

After reading Harper’s story, we decided to get in touch with her parents to offer them a free photoshoot of their beautiful daughter so that they will forever have precious memories of her. Harper had a rare genetic condition and had a bucket list in place at the age of six months old.

Harper had Type 2 Gaucher Disease: This is a very rare, rapidly progressive form of Gaucher Disease which affects the brain, spleen, liver, lungs and bones. It is characterised by severe neurological involvement in the first year of life. Fewer than one in one hundred thousand newborn babies have Type 2 Gaucher Disease. This form of disease shows no ethnic predilection and the vast majority of children die by the age of two years. Sadly, there is no cure or treatments for this disease.

Unfortunately, Harper passed away on the 13th October 2018.

Rest in peace angel: 15.02.2018 - 13.10.2018

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Newcastle Upon Tyne

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