Local Lib Dem councillors have expressed dismay that Haringey Council is planning to demolish the “Log Cabin” in the park at the end of Falkland and Fairfax Roads. It was closed without warning within days of the Council election back in May on health and safety grounds. Harringay ward’s two Liberal Democrat councillors were dismayed to discover that the Labour-run Council’s consultation on the issue will not address the demolition, which will proceed no matter what the outcome.
Harringay Lib Dem Councillors Karen Alexander and Carolyn Baker are urging local residents to attend the Council’s consultation session at the St. John the Baptist Church Hall in Frobisher Road., to be held on 19th October 2006 between 2 pm and 8 pm, to ensure the Council know how local people feel about their plans.
Councillor Alexander comments:
“The Labour council are not planning to ask residents about the decision to knock down the cabin, but instead are asking what should be done with the space. They have not promised a replacement community centre.”
Councillor Baker comments:
“I think it is a shame that the decision to demolish the building was taken without consulting residents. Karen and I will be working hard to seek to ensure that the voices of residents are listened to during the consultation and also ensure that the council provides funding to make this space a real asset to the community.”
over to Trent Park to start the Charity Walk in aid of Motor Neuron Disease. Lots and lots of people turned up for this good cause. Although the disease is incurable, there is much that can be done to make the life lived with the disease better and more enjoyable. The reason they wanted me is that Clare Chadwick, who is the North London organiser of the organization doing the walk, is a local constituent and she was telling me that they need publicity so that the 30% of people who have this disease but who do not beling to the Motor Neuron Disease Association here about it. Support is critical with such an illness – and the 70% of people with the disease who are part of the MND Association can find support, advice and company with others who understand the whole world that surrounds MND. The hope was that the papers might put it in if I showed up and that this might have the affect of reaching those who are not aware of this helpful body.
call of the day is to