On actually doing something 
Author Message
 On actually doing something

 I wrote the following to Kathleen{*filter*}son about all the informative articles
she's been posting and decided to post it for all.  Any "organizers" out there
willing and able to use some of these articles to overcome  the lies.  BY the
way, whatever happened to government "by and for the people"
          What blows ME away is there's all this info. that supports the
"chronic Lyme " diagnosis and those  (deleted) who work for the gov't. agencies
just go on spouting their nonsense.  There was recently a case where some woman
lost her leg but when she applied for workman's compensation she didn't fill
the form out right and they denied her, EVEN AFTER SHE WENT TO THEIR OFFICE
WITH HER ONE LEG.  Our situation reminds of that.  That's why I was talking
about printing your articles and sending them to government officials. I guess
the obvious is for ME to buy a printer and do the work, which I'm too lazy to
do, and ashamed of it.  However, hopefully, at some point, I or someone else
will start working on this.  I still feel that if we can document that we
notified the Dep't. of Health of all this research we can then go to the media
and demand criminal penalties.  But again, if I don't get off my duff and do it
I guess I shouldn't be talking about it.  We don't even know who is on the
OPMC.  Perhaps a Lyme foundation would be willing to use your material to press
for change.  I would be willing to contribute money for this.  In fact, I think
I'll post this on the newsgroup too in case someone more organized than I am
wants to help work on it.  Bob


Thu, 08 May 2003 03:00:00 GMT
 On actually doing something
Good idea Bob, I hate just zipping off replies to articles in the newsgroup and
I'd rather be more effective in actually doing something concrete to futher
research on chronic lyme.  My problem is, I don't know "who" to send articles
to?  Any suggestions?


Thu, 08 May 2003 03:00:00 GMT
 On actually doing something
       Bob,
   The Lyme Disease Foundation has a packet of about thirty articles
reprinted from medical journals that supports chronic Lyme disease.
For a donation, the LDF will mail you copies of the articles. I have found
the articles very helpful in communicating with doctors and when writing
to public officials about chronic Lyme disease. Abstracts of the articles
are listed at this URL.
    http://www.***.com/

    It would be nice to have 50 or 100 medical articles in a booklet that
could be widely distributed to libraries, doctors, patients and the news
media. Every time a doctor or a news article or a public official or an
insurance company made the claim of, "30 days of treatment and you're
cured", the booklet of medical articles could be sent to them. It would be
all of the articles that contradict Steere's theories in one convenient book.
 Aaron  


Quote:
>>I wrote the following to Kathleen{*filter*}son about all the informative articles

she's been posting and decided to post it for all.  Any "organizers" out there
willing and able to use some of these articles to overcome  the lies.  BY the
way, whatever happened to government "by and for the people"
          What blows ME away is there's all this info. that supports the
"chronic Lyme " diagnosis and those  (deleted) who work for the gov't. agencies
just go on spouting their nonsense.  There was recently a case where some woman
lost her leg but when she applied for workman's compensation she didn't fill
the form out right and they denied her, EVEN AFTER SHE WENT TO THEIR OFFICE
WITH HER ONE LEG.  Our situation reminds of that.  That's why I was talking
about printing your articles and sending them to government officials. I guess
the obvious is for ME to buy a printer and do the work, which I'm too lazy to
do, and ashamed of it.  However, hopefully, at some point, I or someone else
will start working on this.  I still feel that if we can document that we
notified the Dep't. of Health of all this research we can then go to the media
and demand criminal penalties.  But again, if I don't get off my duff and do it
I guess I shouldn't be talking about it.  We don't even know who is on the
OPMC.  Perhaps a Lyme foundation would be willing to use your material to press
for change.  I would be willing to contribute money for this.  In fact, I think
I'll post this on the newsgroup too in case someone more organized than I am
wants to help work on it.  Bob>>


Fri, 09 May 2003 14:42:27 GMT
 
 [ 3 post ] 

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