Dysautonomia News - Winter/Spring 2006

The Patient's Voice

 

Views expressed in The Patient's Voice are not necessarily those of the Dysautonomia Information Network or its members.


Share your experiences in The Patient's Voice!

The Patient's Voice is a newsletter column where patients can express themselves while writing about experiences relating to dysautonomia - both positive and negative. It is a place to share medical experiences, suggestions, short stories and poetry, etc. Send contributions to: staff@dinet.org


Medicare Part D
by Gayla Peterson, Louisburg MO.

This Medicare part D
its got the best of me,
but some things are real obvious, you see.
Some silly politician
thinks an Internet magician
resides in every household in the land.

We’re told to go to www dot,
but it’s something many haven’t got;
so how are we supposed to find our way?
When we do get on, it’s too darn hard to do.
After many tries it still asks, “Who are you?”
So then we decide to try another day.

After many days of trying
and several days of crying,
I find that I’m still looking for success.
After many sleepless nights
I vow to keep my fight,
and rise above this senseless, horrible mess!

The companies are many,
some coverage is skimpy,
and then there is the dreaded “coverage gap”;
where, exactly, IS that on my map?
Even my druggist doesn’t know,
exactly where to go.

It’s no wonder that so few
have embraced this thing so new,
the whole thing is just way too confusing.
If it wasn’t for the fact
that I too need to act,
I’d probably find this thing a bit amusing!


 






 

In this Issue:


* President's Message

* Volunteers

* Volunteer Opportunities

* Research in Review

* The Patient's Voice

* Emma's Corner

* Thank You


Dysautonomia News exists to inform and educate. The content should not be used as a substitute for professional medical advice, diagnosis or treatment. Readers are encouraged to confirm all information with other sources and a physician. Please keep in mind that research is evolving and future discoveries may change or disprove some currently held beliefs.
 

Does your place of business or family give to charity? If so, please let them know about the Dysautonomia Information Network, www.dinet.org. DINET is completely funded by member’s donations and can’t exist without them. Thank you!

Dysautonomia News is a quarterly publication of the Dysautonomia Information Network.
Subscribe to Dysautonomia News at www.dinet.org/join.htm