Fab Four To Appear In Croydon: Rare Beatles Memorabilia Included In Auction

beatlesmemorabliaThe Beatles have been fascinating us for over five decades, but it was in 1964, exactly 50 years ago, that they took the world by storm. They appeared on US TV and performed in front of a 73 million audience. Beatles merchandise started to become big business.

Catherine Southon is pleased to announce that she will have not just one, but three rare Beatles memorabilia included in her next sale at The Chateau in the Shirley Hills, near Croydon, on Wednesday, 26th March 2014 at 11.30 am.

By far the most sought after is the 1964 NEMS record player, which is one of the earliest Beatles merchandise – only 5,000 were ever made and they rarely come up for sale. This one is not in mint condition, but will still make a fan’s heart beat faster. The iconic record player has got a print of the Fab Four playing their instruments and facsimile autographs. It is estimated to fetch between £1,000-2,000.

Also from around 1964, is the boxed set of car mascot Bobb’n Head Beatles dolls, which is expected to sell for £300-400. The set is in its original, slightly damaged box and each Beatle plays his instrument. The dolls are about 8” tall and are very popular with collectors.

For fashion conscious ladies, who want to fully embrace Beatlemania, the third Beatles’ lot will be of particular interest. A 1964 Dutch Polka Dot mini dress in beige and white with the faces of John, Paul, George & Ringo printed in black vertically next to a guitar with their facsimile signatures. It’s in excellent condition and a size 10/12 and comes with an estimate of £150-250.

Catherine Southon, well-known through various BBC Antiques programmes, says: “I was really excited to be shown the Beatles memorabilia at a recent valuation day. Although they did not belong to anyone famous, the fact that they have survived for this long in such good condition is quite remarkable. The Beatles are still seen as the greatest and most influential rock band and I know that their fans are always keen to add rare merchandise to their collections.”

Other lots with famous signatures included in the auction is a handbag signed by Neil Armstrong in the mid 1980s. He signed the beaded bag for its owner at a charity event shortly before he stopped giving autographs (estimate £1,000-2,000).

A catalogue will be available from the end of February and the sale can be viewed on 25th & 26th March at The Chateau, Coombe Lane, Shirley, Surrey CR0 5RE.

For more details, please visit www.catherinesouthon.co.uk or call 07808 737 694.

 

Sonic Editions: Impossibly Cool Photography

Sonic Editions produces limited edition, rare, photographic prints of iconic figures throughout time. It’s everyone from Audrey Hepburn through to Jay-Z. There’s some great shots of the likes of Michael Jackson, Sophia Loren, Michael Caine, Al Pacino and Clint Eastwood

The Sonic Editions team has visited the Getty archives in LA and went through 2,000,000 images or so to pull out some totally unseen images.

These specific images are limited to fifty of each and they start from £69. Each image is numbered so that they know what number they own, as well as containing details about the photographer and when it was shot.

Krabbe: The Disease That Needs More Awareness

I had not heard of Krabbe disease until 2011, when a relative was diagnosed with it. Krabbe is also called Globoid cell leukodystrophy; Galactosylcerebrosidase deficiency; Galactosylceramidase deficiency. It is a rare genetic disorder of the nervous system and is a type of leukodystrophy. It is named after the Danish neurologist Knud Haraldsen Krabbe who discovered it.

Krabbe disease is caused by a defect in the GALC gene. People with this gene defect don’t make enough of a substance called galactocerebroside beta-galactosidase (galactosylceramidase).

This is needed by the body to make myelin, the material that surrounds and protects nerve fibers. Myelin breaks down without it, brain cells die, and nerves in the brain and other body areas do not work properly.

There are two forms of Krabbe disease.

  • Early-onset Krabbe disease appears in the first months of life.
  • Late-onset Krabbe disease begins in late childhood or early adolescence.

Krabbe disease is inherited, which means that it runs in families. To get this disease, each of your parents must pass you a copy of the faulty GALC gene.

This condition is very rare, Affecting 1 in 100,000 births.

Symptoms

  • Changing muscle tone from floppy to rigid.
  • Hearing loss that leads to deafness
  • Feeding difficulties
  • Irritability and sensitivity to loud sounds
  • Severe seizures
  • Unexplained fevers
  • Vision loss that leads to blindness
  • Vomiting

The condition is often misdiagnosed as cerebral palsy.

There is no specific treatment for Krabbe disease.It is possible to have a bone marrow transplant in the early stages of the disease, but this treatment has risks.The outcome of Krabbe is usually not good. On average, infants with Krabbe die before age 2. People who develop the disease at a later age have survived into adulthood with nervous system disease.

A blood test can be done to see if you carry the gene for Krabbe disease and prenatal tests can be done to screen a developing baby for this condition.

http://www.savebabiesuk.org/

United Leukodystrophy Foundation — www.ulf.org

http://www.krabbes.com/

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