Save Aarnav from MPS VI

Save Aarnav from MPS VI

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This page is dedicated to a very special child Aarnav a patient of a very rare disease called MPS VI. Aarnav was born a robust baby boy.

Hearing the news that your child has a rare disease is life shattering. It takes time to absorb the words you just heard, process the information and then try to understand what life will look like going forward. For some, the road to diagnosis is not a clear path but an odyssey where families take their sick child from doctor to doctor for years looking for an answer. He was always plagued with t

Photos from Chailey Heritage Foundation's post 20/07/2023
08/02/2021

it’s snowing 🌨

31/12/2020

Wishing you a VERY HAPPY NEW YEAR

25/12/2020

Merry Christmas 🎄

28/11/2020

Not a good weekend for Aarnav😔😔 Chhatrapal Sharma Rajani Sharma

16/09/2020

Some home schooling and self learning by Aarnav

07/09/2020

Today, Aarnav visited Orthopaedic clinic at GOSH Hospital for his Spinal problem. He was earlier diagnosed for Kyphosis which is very common in MPS VI patients.
Kyphosis is a spinal disorder in which an excessive outward curve of the spine results in an abnormal rounding of the upper back.
Aarnav has been advised to wear a brace at least 16 to 18 hours a day as shown in the pic below..

01/09/2020

We worry every time we go to see a doctor because we don't know what they are going to find, but we are not going to give up no matter what now, he is such a great little boy, and we are so happy with him. We are positive for him, and we hope that we can help him do so much in his life. MPS Society UK National MPS Society Mps Papas The Irish MPS Society LSDSS - Lysosomal Storage Disorders Support Society - India

Photos from Save Aarnav from MPS VI's post 01/09/2020

As special needs parents we don’t have the power to make life “fair,” but we do have the power to make life joyful.

Suctioning via a Paediatric Tracheostomy Tube 26/08/2020

This is what Aarnav has to go every 30 minutes, sometimes every 10 minutes 24x7, day and night, since last 2.5 years which makes his daily life more difficult. He feels isolated as he can not go outside and play or talk normally with other children. There is always a fear of infection and Trachy blockage. Parents have to carry an Emergency Kit and Suction Machine all the time with him.

Suctioning via a Paediatric Tracheostomy Tube National Tracheostomy Safety Project. This short video explains how to suction via a paediatric tracheostomy tube; what steps might be necessary in the event...

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