Hello Everyone and thanks to those who contributed to my thread which I started 23 March 2007. Here is the link to remind you
http://www.alzheimers.org.uk/talkingpoint/discuss/showthread.php?t=5953
I have just heard from our lawyer, who was handling probate, and he states this
I have now heard from the Council who have backed down in that they do now accept that your Mother was entitled both to sever the joint tenancy of the property and to do what she wanted to with her half share. However, they say that they do consider that your Father's half share does have a market value and have said "......in this particular case, we understand that the property currently stands empty, and therefore we consider that the property could be sold in order for Mr xxxxx's share to be realised."
This is good news. As is often stated we have won the battle but not the war. The next step is to prevent the house from being sold arguing that the children (my two sisters and I) own one half and don't want to sell and that my sister 'X' is EPA and has stated that it is not in our father's interest. Our father has late stage Alzheimers with Parkinsons, glaucoma, diebetes and thalassemia (a B12 cross link). The reason: it is not in his best interest. I have already spent four weeks in the house this year (I am a Finnish resident). My family who live in other parts of the world will do the same. This is for the well being of my father.
Anyway I thought those who helped in this forum before may want an update. It seems that a PCT even if they know the outcome can challenge with impunity and drain vital resources (emotions, time and money) from a grieving family.
I went back 2 weeks ago to start the process of fully funded NHS continuing care and have written reports to Social Care for an erroneous assessment reported 3 weeks ago and to a PCT Dr questioning the administration of medication. During this time we managed to get father into the adjoining EMI wing, well actually the move is Saturday so I am flying back to Peterborough this Friday.
I would also like to thank in this forum the local Peterborough Alzheimers Branch who have been more than supportive in the matter of my father.
Regards
Brian
http://www.alzheimers.org.uk/talkingpoint/discuss/showthread.php?t=5953
I have just heard from our lawyer, who was handling probate, and he states this
I have now heard from the Council who have backed down in that they do now accept that your Mother was entitled both to sever the joint tenancy of the property and to do what she wanted to with her half share. However, they say that they do consider that your Father's half share does have a market value and have said "......in this particular case, we understand that the property currently stands empty, and therefore we consider that the property could be sold in order for Mr xxxxx's share to be realised."
This is good news. As is often stated we have won the battle but not the war. The next step is to prevent the house from being sold arguing that the children (my two sisters and I) own one half and don't want to sell and that my sister 'X' is EPA and has stated that it is not in our father's interest. Our father has late stage Alzheimers with Parkinsons, glaucoma, diebetes and thalassemia (a B12 cross link). The reason: it is not in his best interest. I have already spent four weeks in the house this year (I am a Finnish resident). My family who live in other parts of the world will do the same. This is for the well being of my father.
Anyway I thought those who helped in this forum before may want an update. It seems that a PCT even if they know the outcome can challenge with impunity and drain vital resources (emotions, time and money) from a grieving family.
I went back 2 weeks ago to start the process of fully funded NHS continuing care and have written reports to Social Care for an erroneous assessment reported 3 weeks ago and to a PCT Dr questioning the administration of medication. During this time we managed to get father into the adjoining EMI wing, well actually the move is Saturday so I am flying back to Peterborough this Friday.
I would also like to thank in this forum the local Peterborough Alzheimers Branch who have been more than supportive in the matter of my father.
Regards
Brian
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