We’ve changed our name!

  We’ve been talking about this for a long time now, so we’re really pleased to have finally changed our name.  Previously known as LPLD Alliance we hope our new name captures the essence both of managing the condition on a daily basis, and the work of the charity on behalf of people affected by…

Read More

John

John

I was born in London in 1954 and I diagnosed with what was the called Hypertriglyceridaemia at the age of 11. My parents realised I had the problem following the diagnosis of my younger sister Jill, as I always had stomach aches and pains after Sunday roasts and fried foods.

Read More

Pat

Pat

I understand from my mother, that the symptoms of my condition of FCS ( not called that back in 1955) came to light when I was 6 weeks old when the milk feed I was on became richer. Until my late teens, all my family and I understood, was that I should avoid dairy rich products and fried food.

Read More

Take our survey

In order to ensure that we’re focusing on what will be the most helpful to you as a member of our community, please fill in our short survey and help us to set our priorities for the next three years.

Read More