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Cathie (46) and Craig (50) Watt are your average Australian family. They have two beautiful children.
Ten years ago Cathie and Craig were given the horrible news that Craig had been diagnosed with Huntingtons disease, an inherited disorder that results in death of brain cells.
The earliest symptoms are often subtle problems with mood or mental abilities. A general lack of coordination and an unsteady gait often follow. As the disease advances, uncoordinated, jerky body movements become more apparent. Physical abilities gradually worsen until coordinated movement becomes difficult and the person is unable to talk. Mental abilities generally decline into dementia. The specific symptoms vary somewhat between people. Symptoms usually begin between 30 and 50 years of age, but can start at any age. The disease may develop earlier in life in each successive generation. About 8% of cases start before the age of 20 years and typically present with symptoms more similar to Parkinson's disease. People with HD often underestimate the degree of their problems.
At this stage Craig is suffering the worst of the symptoms associated with huntingtons disease and often struggles with his mobility and speech, and has been mistaken for being under the influence of alcohol. To explain the disease is laden terms it is though he is struggling with Parkinson's, motor neurone disease and Alzheimers.
The psychological stress that Cathy has suffered as well as what their family is going through is astronomical.
There is no cure for this disease although there are trials running in China for treatment. The goal is to have Craig there as soon as possible, and if anyone could spare as little as $5 it would go a long way toward supporting this family to have a better future.
The family themselves, including their children do not wish to be contact, are not looking for any sympathy, and did not set up this page. But as a friend, I know there are a lot of people who care enough to help!
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