Next week I have my first appointment with the Biologics team since the switchback to Humira. Usually a routine six-monthly check up but the significance of this one is that it’s three months since I restarted on Humira – and three months is the period in which you are told[Read More…]
As some of you know, I’ve been experiencing some brand new symptoms of late that are really getting me down, multiple infections, crippling fatigue, all over joint pain and night sweats to name but a few. After recently reading Lindsay Reid’s poetry based on her experiences living with Ankylosing Spondylitis[Read More…]
Its alcohol awareness week this week in the UK and many people often overlook the links between alcohol and psoriasis. I was always a big social drinker, it went with the territory of playing team sport every weekend but as my health deteriorated and I was diagnosed with yet another[Read More…]
