This is topic Crappy Doctor's Appt Today with Steere's Friend! in forum General Support at LymeNet Flash.


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Posted by Teresa Pratt (Member # 12129) on :
 
I know you all are going to scream at me for not going to a llmd BUT because of financial obligations I have not done so. Because of many problems I am having including high white blood cell count, burning bones, sore muscles, stiffness, headaches (and the list goes on and on), I went to my family doctor to see if I could get anywhere with her. She's very nice, and wants to help, but doesn't know much. She did a bunch of blood tests that came out negative, except for two. One was my white blood cell count which was high, but not horrible (12,200). And my Western blot which showed "I had lyme disease a long time ago".

So, she sends me to an infectious disease doctor.

I waited SEVEN WEEKS for this appt, AND locked my keys in the car when I got there!!!

You're going to love this...

Turns out this guy's friends with Alan Steere! He starts telling me about this whole "underground group" on the internet and how they picket with signs outside of his practice with signs that read "murderer"!

He told me that my Western Blot is showing some antibodies because when I got bit one year ago and had a rash my body developed antibodies against lyme. He also said that since my family doctor treated it promptly with 20 days of antibiotics, I no longer have lyme. But the good news is that now I have lyme antibodies in my system that will help me not catch lyme disease in the future!!! Well I guess I don't have to worry about the 10-15 deer ticks that have bitten me since then.

Needless to say, I am pretty mad about this appt. I questioned him about the reliability of the Western Blot and gave him the information about the CENTRAL FLORIDA RESEARCH, INC. He told me that there are many bogus labs out there offering crazy tests. He asked if the test has been approved by the FDA. I told him I didn't know, and he handed the papers that I printed out back to me.

He told me that I'm fine, I do not have lyme disease, and if my joints hurt I should see a rhumatoid (sp) doctor. There really was no reason that my family doctor should have sent me to him.

Oh Well...

Could anyone tell me if the Central Florida Lab test has been approved by the FDA? Since I have a half decent family doctor, I want to go back to her and ask her to test me, but I'm afraid that she will ask me about the FDA as well.

Thanks!
 
Posted by Lymetoo (Member # 743) on :
 
quote:
Originally posted by Teresa Pratt:

Turns out this guy's friends with Alan Steere! He starts telling me about this whole "underground group" on the internet and how they picket with signs outside of his practice with signs that read "murderer"!

YES...That would be US!! [Big Grin] [lol]
 
Posted by Lymetoo (Member # 743) on :
 
quote:
Originally posted by Teresa Pratt:

He also said that since my family doctor treated it promptly with 20 days of antibiotics, I no longer have lyme. But the good news is that now I have lyme antibodies in my system that will help me not catch lyme disease in the future!!!

HA!

Could anyone tell me if the Central Florida Lab test has been approved by the FDA?

The FDA S***S!!

Since I have a half decent family doctor, I want to go back to her and ask her to test me, but I'm afraid that she will ask me about the FDA as well.
[/QB]

Don't worry about it....it's YOUR body!! You deserve to be WELL!!

Find a dr willing to run a WB through Igenex.
 
Posted by Teresa Pratt (Member # 12129) on :
 
I figured it was you (us) troublemakers!!! Boy, let me tell you this doctor REALLY hates us. This is good, that means we are being heard, and we are being a thorn in their side!!!

What I can't figure out is why the perv made me get naked to listen to my heart, lungs and press on my stomach? Can't you do the same thing with your clothes on? Especially when he ALREADY determined that I didn't have lyme disease and that I shouldn't be there!!! [bonk]
 
Posted by meg (Member # 22) on :
 
[lol]
 
Posted by Tincup (Member # 5829) on :
 
[puke]

Ahhhhhhhhhhhhhhhhhhhhhh!! What a nightmare!

Can you write the date, time of your appt and where it was.. and send it with a VERY BRIEF facts only... no "story" details needed.. to the LDA?

They are collecting this type of information. it could help ALL of us if you would.

Sorry you got a Bumsteere butt kissing duck.

And from what you've said.. it appears these dopes are getting dumber by the day!

AND they are scared.. you are right.. and guilty about something or they wouldn't "hate" patients so much!

I wonder what other patients would do if they were diabetic and depended on their insullin and it was taken away?

Mothers, individuals and families would be completely FREAKED OUT!

So I think we are rather mild, considering...

[Big Grin]
 
Posted by Michelle M (Member # 7200) on :
 
I rather favor something like this:

"Dear Dr. __________:

"Fortunately, the crazy people at LymeNet have helped educate me, and I now know that having lyme in the past does not confer immunity to reinfection. I quake to think of your dispensing such misadvice regularly to patients with equanimity. Go look that up. Equanimity, that is, not immunity.

Fortunately, I now know that IgM and IgG antibodies in lyme disease are a very uncertain indicator of present infection status, and that in fact, people with late stage lyme are much more likely to have positive IgM. Significant antibody response on either marker, coupled with symptoms and exposure, should be treated.

Fortunately, I have read the dozens of articles documenting the persistence of borrelia burgdorferi in spite of repeated rounds of antibiotics. Clearly you and Dr. Steere have not read these. You are an embarassment to your profession.

Fortunately, I now know that the lyme specialty lab IGeneX has all required approvals and accreditations and in fact regularly outperforms most labs you would deem appropriate since it uses more than one strain of bacteria with which to test.

Thank you for your abyssmal lack of knowledge. Please don't send me a bill.

Sincerely,

Teresa"
 
Posted by Ellie K (Member # 12056) on :
 
Michelle, that letter is perfect. Just beautiful. [lol]
 
Posted by bettyg (Member # 6147) on :
 
[lol] [lol] Michelle M, fantastic letter with your legal background and all! [bow] [bow]

Teresa, so sorry to read about your mistretment today and then forced to strip for nothing; and shouldnt have had anyway!

please do as tincup suggested; we need more evidence against these bozos. [cussing]
 
Posted by Geneal (Member # 10375) on :
 
I would add to that letter that not only is this doctor and Steere an embarassment

To their profession, their lack of credible knowledge regarding TBD's puts

Patients' lives at risk.

There is no such thing as "building" an immunity to bb.

That is total hogwash.

If I get bit again, I can get Lyme again.....and again, and again......

Please save your money as well as yourself by seeing a LLMD.

Your life is worth every penny.

I like being part of the "underground crazies!"

It is like being part of a covert operation.

Thank God for lymenet. I believe that this site has saved my life and sanity (what's left of it anyways).

Hugs,

Geneal
 
Posted by Teresa Pratt (Member # 12129) on :
 
Thank you all for your responses. Yesterday, I felt angry, helpless and violated. I was not sure which direction to go in. Rest assured, I will write both letters TODAY! At least that will make me feel like yesterday was not a complete waste of time

Most of you don't know that I have been a "lurker" on this board for about 5 years, because my husband got bit 5 years ago and was very, very ill. I used to use the name "wildthing". (but I lost my password and had to re-register.) I don't post much, I just read alot of the posts and info and compare my symptoms with yours. Sometimes, being an "lurker", I wonder, can all of this truly be real? Are things really this bleak? Are doctors really this ignorant and misinformed? Well, yesterday was a wake up call for me. If anyone out there is lurking and wondering if this is for real, please know that yes, it is this bad, and worse, when you have to go through it yourself.

Thanks again!
Teresa [hi]
 
Posted by lou (Member # 81) on :
 
I would not mention any good labs that test for lyme to ducks. This is like waving a red flag in front of a bull and they could and have caused trouble for labs and docs.

Also, once a duck has revealed himself/herself to be a friend of Steere and one who hates lyme patients, there is no point in handing them any information whatsoever, or trying to debate it. Just raises the blood pressure and upsets the victim/patient. And you know what they say about trying to teach a pig to dance: it annoys the pig and will not succeed anyway. So then you have a mad pig that can't dance, and you have wasted your time.
 
Posted by Lymetoo (Member # 743) on :
 
quote:
Originally posted by Ellie K:
Michelle, that letter is perfect. Just beautiful. [lol]

[Big Grin]
 
Posted by CaliforniaLyme (Member # 7136) on :
 
I wish I knew how to do that LymeToo!!! Michelle M Michelle M Michelle Michelle Michelle- that was

p e r f e c t.


Teresa, we could always FEEL you lurking*)!*)!!
Sorry you had to go through that- you deserve
MUCH better!!!!!!!!!!
 
Posted by CaliforniaLyme (Member # 7136) on :
 
p.s. There is a proud history in this country of underground movements- I have always thought of us as The Underground Railroad for Lymies anyway*!))! Harriet Tubman would be proud!*)*)!!
 
Posted by lymednva (Member # 9098) on :
 
California Lyme said,
quote:
I have always thought of us as The Underground Railroad for Lymies anyway*!))! Harriet Tubman would be proud!*)*)!!
Great analogy! [Big Grin]
 
Posted by Lymetoo (Member # 743) on :
 
quote:
Originally posted by CaliforniaLyme:
I wish I knew how to do that LymeToo!!!

Do what?
 
Posted by CaliforniaLyme (Member # 7136) on :
 
(Sorry guys not topical!! Makes things dark like that!!! Emphasize them!!! It is very cool-))
 
Posted by Lymetoo (Member # 743) on :
 
You click on the Quote symbols and it does it for you. Or you can type [b] and then bracket /b] .. also put in the first bracket before the /b That will make it bold.

It will then "hide" the b's .. that's why I couldn't do the whole thing...it would "erase" the b's. BOY, that doesn't make sense! [Roll Eyes]
 
Posted by CaliforniaLyme (Member # 7136) on :
 
[b Thank you*)!*! b]
 
Posted by Soleilpie (Member # 8481) on :
 
Where on earth did this doc get the idea that once you get Lyme, you're immune to a 2nd or subsequent infection?

Talk about misinformation and a dangerous one to boot!
 


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