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soc / soc.support.stroke / Stroke Survivor's Bill of Rights

SubjectAuthor
* Stroke Survivor's Bill of RightsMyhome
`- Re: Stroke Survivor's Bill of RightsHigh Miles

1
Subject: Stroke Survivor's Bill of Rights
From: Myhome
Newsgroups: soc.support.stroke
Organization: A noiseless patient Spider
Date: Thu, 4 Nov 2010 19:34 UTC
Path: eternal-september.org!news.eternal-september.org!reader01.eternal-september.org!reader02.eternal-september.org!news.freedyn.de!not-for-mail
From: myhome@mts.net (Myhome)
Newsgroups: soc.support.stroke
Subject: Stroke Survivor's Bill of Rights
Date: Thu, 04 Nov 2010 14:34:21 -0500
Organization: A noiseless patient Spider
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What I Needed Most from My Family, Friends and Myself

1. I needed you to treat me like I was going to recover completely. It
might take two years or five years or a lifetime, but I needed to be
treated like I was going to recover completely.

2. I needed you to honor the healing power of sleep. The brain is a
brilliant machine that processes trillions of bits of data every
moment. The brain uses sleep to shut down incoming stimulation and
create order out of the day's events. In the beginning, my brain
wanted to sleep a lot. I believe that it was partially because we
honored the healing power of sleep that my brain recovered so well.

3. I needed to challenge my brain systems immediately. I understood
that connections in my brain had been broken, and it was critically
important that I challenged the system before more cells had a chance
to die. When awake, I was always given choices - did I want this or
that to eat, did I want to do this or that. I was forced to answer
questions that made me think, instead of yes/no questions that
required nothing from me.

4. I needed you to love me - not for the person I was before, but for
who I might become. The woman I had been died that morning. With my
left hemisphere no longer functioning, I needed people to love me for
who I had become. I might have looked the same and sounded the same,
but I was different - and that had to be OK.

5. I needed to define my priorities for what I wanted to get back the
most. I lost my ability to speak and understand language, to walk and
drive, as well as all my science and math abilities. Because I had
very limited energy, I had to focus my time. I realized that I night
never be a scientist again, but I had a message to communicate about
the beauty and resiliency of the brain. I chose to focus my energy on
public speaking. Because speaking on the telephone was an obvious
energy drain for me, my family protected me by not letting me speak on
the phone. That was a lot of help.

6. I needed you to focus on my ability, not my disability. I needed to
celebrate everything. If all I was doing was breathing, then we could
celebrate that I was alive - and breathe deeper together. If I
stumbled, then we could celebrate when I was upright! If I was
drooling, we could celebrate my swallowing! It was way too easy to
focus on my disabilities because they were vast, I needed you to
celebrate my triumphs every day! My successes, no matter how small,
inspired me.

7. I needed to allow myself to receive support, love, help. It would
be at least two years before we really knew how extensive my recovery
would be. I needed to get out of my own way. I needed to stop beating
on myself for being less. I needed time to let my brain heal. I needed
you to cut me some slack and not be so heavy all the time! I was not
less, I was different, and it's OK to be different.

8. I needed to divide every task into smaller and simpler stages or
steps of action. Instead of rolling over, I might rock. Instead of
standing up, I might sit and rock. Just because you could not see that
I was trying, it did not mean that I was not trying. Sometimes when I
was tired, I just needed to sleep, and I needed you to just accept
that.

9. I needed you to assume that I knew nothing, I had, after all, lost
my mind. Pieces of information did not fit together anymore in my
brain; for instance, I might not know what a fork was. I might not
know what a shoe was -much less that my socks went on first and why.
As my caregiver, you were my teacher. It helped when you talked to me,
repeated yourself and didn't act like I was stupid if I didn't get it
the first 20 times! Raising your voice did not help you communicate
with me. I was not deaf, I was wounded.

10. I needed you to come close and not be afraid of me. I needed you
to touch me, stroke my arm, my hair, and wipe my face if I was
drooling - to be kind to me. What you said was not as important as how
you said it. What you did was not as important as how you did it. It
helped when you came close and enunciated clearly. If you brought your
best self forward, my spirit would greet you - only when I trusted you
as a caring giver would we heal my brain together.

Subject: Re: Stroke Survivor's Bill of Rights
From: High Miles
Newsgroups: soc.support.stroke
Organization: Public Usenet Newsgroup Access
Date: Thu, 4 Nov 2010 19:51 UTC
References: 1
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From: 2blues1723@comcast.net (High Miles)
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Subject: Re: Stroke Survivor's Bill of Rights
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Date: Thu, 04 Nov 2010 14:51:14 -0500
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This is excellent and should appear on the wall in every stroke
patient's room.

On 11/4/2010 2:34 PM, Myhome wrote:
> What I Needed Most from My Family, Friends and Myself
>
> 1. I needed you to treat me like I was going to recover completely. It
> might take two years or five years or a lifetime, but I needed to be
> treated like I was going to recover completely.
>
> 2. I needed you to honor the healing power of sleep. The brain is a
> brilliant machine that processes trillions of bits of data every
> moment. The brain uses sleep to shut down incoming stimulation and
> create order out of the day's events. In the beginning, my brain
> wanted to sleep a lot. I believe that it was partially because we
> honored the healing power of sleep that my brain recovered so well.
>
> 3. I needed to challenge my brain systems immediately. I understood
> that connections in my brain had been broken, and it was critically
> important that I challenged the system before more cells had a chance
> to die. When awake, I was always given choices - did I want this or
> that to eat, did I want to do this or that. I was forced to answer
> questions that made me think, instead of yes/no questions that
> required nothing from me.
>
> 4. I needed you to love me - not for the person I was before, but for
> who I might become. The woman I had been died that morning. With my
> left hemisphere no longer functioning, I needed people to love me for
> who I had become. I might have looked the same and sounded the same,
> but I was different - and that had to be OK.
>
> 5. I needed to define my priorities for what I wanted to get back the
> most. I lost my ability to speak and understand language, to walk and
> drive, as well as all my science and math abilities. Because I had
> very limited energy, I had to focus my time. I realized that I night
> never be a scientist again, but I had a message to communicate about
> the beauty and resiliency of the brain. I chose to focus my energy on
> public speaking. Because speaking on the telephone was an obvious
> energy drain for me, my family protected me by not letting me speak on
> the phone. That was a lot of help.
>
> 6. I needed you to focus on my ability, not my disability. I needed to
> celebrate everything. If all I was doing was breathing, then we could
> celebrate that I was alive - and breathe deeper together. If I
> stumbled, then we could celebrate when I was upright! If I was
> drooling, we could celebrate my swallowing! It was way too easy to
> focus on my disabilities because they were vast, I needed you to
> celebrate my triumphs every day! My successes, no matter how small,
> inspired me.
>
> 7. I needed to allow myself to receive support, love, help. It would
> be at least two years before we really knew how extensive my recovery
> would be. I needed to get out of my own way. I needed to stop beating
> on myself for being less. I needed time to let my brain heal. I needed
> you to cut me some slack and not be so heavy all the time! I was not
> less, I was different, and it's OK to be different.
>
> 8. I needed to divide every task into smaller and simpler stages or
> steps of action. Instead of rolling over, I might rock. Instead of
> standing up, I might sit and rock. Just because you could not see that
> I was trying, it did not mean that I was not trying. Sometimes when I
> was tired, I just needed to sleep, and I needed you to just accept
> that.
>
> 9. I needed you to assume that I knew nothing, I had, after all, lost
> my mind. Pieces of information did not fit together anymore in my
> brain; for instance, I might not know what a fork was. I might not
> know what a shoe was -much less that my socks went on first and why.
> As my caregiver, you were my teacher. It helped when you talked to me,
> repeated yourself and didn't act like I was stupid if I didn't get it
> the first 20 times! Raising your voice did not help you communicate
> with me. I was not deaf, I was wounded.
>
> 10. I needed you to come close and not be afraid of me. I needed you
> to touch me, stroke my arm, my hair, and wipe my face if I was
> drooling - to be kind to me. What you said was not as important as how
> you said it. What you did was not as important as how you did it. It
> helped when you came close and enunciated clearly. If you brought your
> best self forward, my spirit would greet you - only when I trusted you
> as a caring giver would we heal my brain together.

1

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