I am curious what happens in an occupational therapy assessment and follow up.
In October, my neuro gave me a referral for OT, and I have an appointment scheduled next week. For some background, I am 42 and have been dx with MS for 16 years. Except for regular exacerbations the first 5 years or so, I have been highly functional.
However, in February of this year, I went on "short" term diability from my job, which turned into full time disability. This followed a cognitive assessment in May which showed significant impairments in a number of areas, most debilitating in executive function.
I am married with two girls (grades 3 and 5). I wish I could remember all of the areas that I have problems with, but daily living has been difficult. I do not cook (anymore) as I cannot reliably follow even the simplest of directions - written or verbal.
Mostly I am worried that the OT evaluation will result in "lists" for me to follow, which is a concern.
If anyone has had OT experience, I would appreciate your perspective on its value to you.
In October, my neuro gave me a referral for OT, and I have an appointment scheduled next week. For some background, I am 42 and have been dx with MS for 16 years. Except for regular exacerbations the first 5 years or so, I have been highly functional.
However, in February of this year, I went on "short" term diability from my job, which turned into full time disability. This followed a cognitive assessment in May which showed significant impairments in a number of areas, most debilitating in executive function.
I am married with two girls (grades 3 and 5). I wish I could remember all of the areas that I have problems with, but daily living has been difficult. I do not cook (anymore) as I cannot reliably follow even the simplest of directions - written or verbal.
Mostly I am worried that the OT evaluation will result in "lists" for me to follow, which is a concern.
If anyone has had OT experience, I would appreciate your perspective on its value to you.
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