In May, after 3 months of "short term disability" from my job, I had a neuro-cognitive assessment. The results were poor and indicated significant loss of cognitive function. Shortly before my cognitive assessment, I lost my job as an executive lobbyist for a non-profit business organization.
I have moved to "long term disability" and am now in the process of trying to figure out how to live independently. The process is difficult as I am unable to develop strategies to address the difficulties I have with daily living.
One of the most basic problems I have is answering the question "What can I do to help" that people have asked me. I know that I need help, but I simply do not know what to ask for.
Because I have income through disability insurance, I do not qualify for county social services. I have an appointment on Oct 21 and am planning to ask my neuro for a referral for an OT assessment, which I hope my medical insurance will cover.
I have enjoyed reading the posts on this website and look forward to being more connected with others who also live with ms.
I have moved to "long term disability" and am now in the process of trying to figure out how to live independently. The process is difficult as I am unable to develop strategies to address the difficulties I have with daily living.
One of the most basic problems I have is answering the question "What can I do to help" that people have asked me. I know that I need help, but I simply do not know what to ask for.
Because I have income through disability insurance, I do not qualify for county social services. I have an appointment on Oct 21 and am planning to ask my neuro for a referral for an OT assessment, which I hope my medical insurance will cover.
I have enjoyed reading the posts on this website and look forward to being more connected with others who also live with ms.
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