I am just checking in after a long gap. I joined this wonderful forum 6 years ago shortly after my PV diagnosis and was a regular reader and contributor here. In the early days I gained a better understanding of my condition by my questions on here and attended excellent informative days run by Maz at Christie’s in Manchester. I last wrote on here three years ago when I was at a very low ebb and shared my feelings with you as my husband Roger was suffering from multiple myeloma. The support and empathy from all who responded was very comforting to me.
Roger passed away in September 20. My devastation was immeasurable made many times worse by the restrictions of lockdown. A funeral with limited numbers, where no one could shake my hand or give me a hug was tough. I could write forever on the inefficiencies of organisations at that time with whom I was single handedly dealing and if I started on DVLA I could bore you to tears.
Life has changed for me and now on the whole I feel that I am making some slow progress. My background as a counsellor/psychotherapist has helped me to really understand and to be honest with myself and others regarding my feelings. I very much realise the importance of my self care.
Recently I have been reading the odd post on here and now I feel ready to be part of this wonderful group again.