Woodleigh Research Facility

Woodleigh Research Facility in memory of Isaac Turner

Fundraising for The Society For Mucopolysaccharide Diseases (The MPS Society)
by 67 supporters
In memory of Isaac Turner
The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
We support affected individuals & families to raise awareness of MPS diseases


Words By Nina Walsh : 

My thoughts have been very much with Adam and Isaac Turner this last week.

For those of you who don't know Adam, he writes a fantastic blog https://baggingarea.blogspot.com

More of a musical historian than a blogger.

Baggingarea has always been the one stop shop that Andrew and I would visit when we needed to remember something about ourselves!

Sadly his son, Isaac, who brought so much joy to so many via his pictorial everyday doings posted on social media, passed away last week and many a heart has been broken.

Isaac lived with a condition called Mucopolysaccharide disease (MPS), a condition I knew nothing about until getting to know Isaac, albeit through pixels alone. He was a brave young man with a terrific smile and we will all miss him dearly. My deepest condolences to Adam and the Turner family.

As a way to raise some funds for the MPS Society I have decided to auction Andrew's beloved 39p Museum that was curated over the duration of our partnership from Facilities 1 to 4. I will also include the original reference CD master of Convenanza, mastered by Noel Summerville at 3345 Mastering, bundled together in a brand spanking new Facility 5 tote bag (awaiting delivery!). 100% of proceeds will go to the MPS Society, payable via the justgiving fundraiser page set up by the marvelous Martin Brannagan of the legendary Flightpath Estate Facebook page. There is also the option to just donate if you are feeling generous 🙂 

The auction will end at midnight Christmas Eve.
Bids in the comments on the thread on the Woodleigh Research Facility facebook page, https://www.facebook.com/Woodleigh-Research-Facility-759003620871949

Do I hear £10?


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About the charity

The Society For Mucopolysaccharide Diseases (The MPS Society)

Verified by JustGiving

RCN 1143472 and Scotland SC041012
The MPS Society provides professional support to children, adults and families affected by MPS, Fabry and related Lysosomal Storage Diseases and funds research into treatment and therapies. These diseases are rare, genetic, life-limiting conditions.

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