This is totally beyond breaking my heart and giving me a cement knot in my stomach. I have not lived with it ~ ~ only vicariously through you and a couple of others. I cannot even imagine the horror.
I can only send hugs and prayers and gentle thoughts.
We are so lucky in the U.K. To have National Health services, the Red Cross, who loan equipment and The Motor Neurone Society for advice. Our hospices offer wonderful respite and if wanted, end of life care. My mother lived for two years after diagnosis and died nearly sixteen years ago. I hope the research that is being carried out will benefit others who suffer from this awful disease.
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This is totally beyond breaking my heart and giving me a cement knot in my stomach. I have not lived with it ~ ~ only vicariously through you and a couple of others. I cannot even imagine the horror.
I can only send hugs and prayers and gentle thoughts.
We are so lucky in the U.K. To have National Health services, the Red Cross, who loan equipment and The Motor Neurone Society for advice. Our hospices offer wonderful respite and if wanted, end of life care.
My mother lived for two years after diagnosis and died nearly sixteen years ago. I hope the research that is being carried out will benefit others who suffer from this awful disease.
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