Fight for Sight
The AK Community
The AK community is a dedicated fund, fighting for better diagnosis, treatment and prevention of Acanthamoeba Keratitis.
Story
Acanthamoeba Keratitis (AK) is a rare but serious infection of the eye, caused by microscopic organisms called Acanthamoeba, which are common in nature in bodies of water such as rivers and lakes, as well as domestic tap water, swimming pools, hot tubs, soil and air. AK is most common in people who wear contact lenses, but anyone with an injury to their cornea, the clear window in the front of the eye, is susceptible to developing this infection. The incidence of this infection appears to be growing, with one London hospital now seeing 50-60 new cases a year, more than double the number ten years ago. Similar increases are reported in many other countries.
In the early stage of infection, the Acanthamoeba eat into the cornea, causing severe pain, loss of vision and extreme photophobia. The infection can often mimic other conditions, making correct diagnosis difficult and delaying appropriate treatment. Treatment generally consists of administering aggressive chemicals to the eye to kill the organisms, often hourly to start with. This treatment usually continues for several months or sometimes even years, during which time sufferers lives are blighted by pain and inability to cope with bright light. A high percentage of sufferers require corneal transplants during or at the end of their treatment and some never recover usable vision in the affected eye. A further difficulty is that these treatments are unlicensed and not covered by medical insurance in many countries.
The AK Community has been set up by patients who have suffered from, and in some cases are still suffering from, the effects of AK. The money raised will help Fight for Sight fund research into more effective treatment and diagnosis of this condition. Many cases could also be prevented by the provision of better information about the infection to contact lenses prescribers and wearers.
Here are the personal stories of two of the members of the AK Community:
"I contracted AK in 2016 at the age of 62, probably from showering while wearing contact lenses Id been wearing contacts for 25 years and no-one had warned me that this was dangerous. I was diagnosed after eight days (which is unusually quick) and sent straight to Moorfields Hospital in London, where I got the right treatment. I suffered terrible pain for many months and had to live in a darkened room, unable to do anything except listen to the radio, but after six months I was free of infection and able to start rebuilding my life. Ive had a few problems since but Im one of the luckier ones most people with AK have far worse outcomes than me. "
Dr Ian West, UK
"I contracted AK in February 2017. I started the AK treatment two weeks later, but the infection was so aggressive that within four weeks of the first signs of AK I needed an emergency cornea transplant to save my eye and eyesight. I have been left with an aftermath of nerve damage (Trigeminal Neuralgia) and severe astigmatism, due to the shape of the new cornea. Nonetheless I am grateful for having been treated so quick and having had the transplant. "
Juliette Vila Sinclair Spence, Netherlands
Although this fund has been set up in the UK, the work it supports is the subject of international and will have world-wide impact.
Our aim is to raise £15,000 in our first year to fund a small research project, with the objective of funding larger projects in the future.
You can read more about the experiences of AK sufferers here.
Here are some links to more information about AK treatment and prevention: