I am new on here. Recently my Dad was diagnosed with suspected Parkinsons, however it looks more like PSP. We have an appointment with the consultant in March. Now it is a waiting game. I look at my Dad and my heart breaks. He had a SAH 3 years ago which has left him with brain damage, dissabilities, aphasia and dysphgia...and now this...all alittle over whelming if I am honest. As soon as I thought life started to settle down this happened. I know we have a long long hard road ahead. So glad to have this forum of people to reach out to.