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» LymeNet Flash » Questions and Discussion » Medical Questions » Bradford Protocol

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Author Topic: Bradford Protocol
cjnelson
LymeNet Contributor
Member # 12928

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May be a can of worms I am opening, as I heard about this for first time today.....so here it goes

anybody with any insight on this one???

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Seeking renewed health & vitality.
---------------------------------
Do not take anything I say as medical advice - I am NOT a dr!
Posts: 830 | From TN | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
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Member # 743

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Refresh my memory!

--------------------
--Lymetutu--
Opinions, not medical advice!
Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
DesperationIn
LymeNet Contributor
Member # 13121

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Wow- I never heard of this one yet. Please share. I am sure it must be better than my drinking urine post- validity aside, I still haven't gotten there just yet [Smile] -Despin
Posts: 163 | From Cleveland, OH | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
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Oh yeah....Dangerous, if you ask me.

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=046095

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--Lymetutu--
Opinions, not medical advice!
Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686

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If you are talking about the Bismacine protocol, my understanding was that someone died from using Bismacine in the US.

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Be well,
Scott
Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
sonicbmx
LymeNet Contributor
Member # 12949

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my Holistic Dr referred me to this guy.. saw him in June. he pricked my finger, smeared blood on a slide, viewed it on

computer via telescope, and claimed i had Fungus in my blood and Lyme was my underlying problem. i became skeptical and started thinking.. was this really MY blood on the monitor?!

here were my red flags:

- he was unable to provide me with a written report or images of his findings

- making the appt was weird and so was his office

- they couldn't create an invoice for my social worker

- the visit was $250, and IV treatment in MEX was $15K

- he claimed i'd be cured in 3 weeks and the IV was illegal in the US (Tx note is chicken scratch.. looks like Sulloxime IV)

i managed to get a copy of the BRI Lyme Report and my Tx notes taken by the so-called MEX nurse. i shared these things with my

Ducks and they were totally against him.. as well as me and my LD suspicions. my Rheumy claimed he was on Quack Watch.

i must admit.. i was tempted to go with his Tx b/c i was desperate and wanted help. my gut changed my mind.

PM me if you want more info or see his website: www.bradfordimc.com.
--
sonicbmx

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"The hell with Drs.. we have each other!"
My story began here:

http://forums.wrongdiagnosis.com/showthread.php?t=16210
http://forums.wrongdiagnosis.com/showthread.php?t=7833
http://forums.wrongdiagnosis.com/showthread.php?t=6873
Posts: 127 | From Van Nuys, CA | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

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I know someone who went there and dropped lots of cash.....only to feel worse.

--------------------
--Lymetutu--
Opinions, not medical advice!
Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
   

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