LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Phototox rxn - 4 mos in dark now Lyme is back!

 - UBBFriend: Email this page to someone!    
Author Topic: Phototox rxn - 4 mos in dark now Lyme is back!
Cx=waspsting
Member
Member # 37685

Icon 1 posted      Profile for Cx=waspsting     Send New Private Message       Edit/Delete Post   Reply With Quote 
Pls help.... I took doxy and palquenil and had a bizarre horrible photo reaction in June.... Truly my whole body lit up as white light ( and I could see it !!) ... Burnt for months and laid in an absolute dark room for months ..... Now crawling out in 40 watt lit basement.... PROBLEM is the CNS Lyme symptoms are back.....so I just took 3 days of Cedax and poof CNS much better BUT phototox is worse!!!! Back to abject darkness.....I cant be treated???!! SCARED .... Any suggestions??? Seems I can't take any antibiotics due to phototox reaction..... Pls help!!! P (ps been to 25+ MDs and not the first one even believes I have any type of adverse health condition....of course I look pretty weird on my opaque frog suit and leather hat and gloves!! So much for objective vs subjective thinking!! Jerks.... They have treated me A's non-human)
Posts: 16 | From Louisville KY | Registered: May 2012  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
I believe you are looking for info on porphyria.

If you use the search button above you will find hundreds of post about this going back many years.

Keebler seems to be the porphyria expert. Actually Keebler is the expert on many lyme & co topics. She always has urls for extensive reading.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6495 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Have you considered trying a Rife machine for the Lyme? (I guess you have Lyme?)

Do you have other coinfections?

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Cx=waspsting
Member
Member # 37685

Icon 1 posted      Profile for Cx=waspsting     Send New Private Message       Edit/Delete Post   Reply With Quote 
Porphyria tests neg - I even repeated them three times b/c realized poor sample handling/lab errors in first two..... Porphyria specialist says .... Not porphyria.....help me someone pls God some window must open after all these doors keep closing shut?!?! P
Posts: 16 | From Louisville KY | Registered: May 2012  |  IP: Logged | Report this post to a Moderator
map1131
Frequent Contributor (5K+ posts)
Member # 2022

Icon 1 posted      Profile for map1131     Send New Private Message       Edit/Delete Post   Reply With Quote 
Come to our next lyme support meeting and I will lend you my rife book called "When Antibiotics Fail...Lyme Disease and Rife Machines".

At our last support meeting we decided to start a library of Lyme books. All of us have so many to share with others.

One must open their heart and mind to all the possiblities that are out there.

Pam

--------------------
"Never, never, never, never, never give up" Winston Churchill

Posts: 6495 | From Louisville, Ky | Registered: Jan 2002  |  IP: Logged | Report this post to a Moderator
sparkle7
Frequent Contributor (5K+ posts)
Member # 10397

Icon 1 posted      Profile for sparkle7     Send New Private Message       Edit/Delete Post   Reply With Quote 
There are herbal alternatives. Maybe try them? Stephen Buhner has a good book on herbal treatent of Lyme. Dr. Cowden, Dr. Klinghardt & Dr. Yang also treat with alternative therapies. There's alot of info here & on the internet if you do some searches.

You may also want to look into the Marshall Protocol...? They actually avoid light as a means of getting well. I don't know too much about it since I never tried it but some people do well with it.

http://bacteriality.com/about-the-mp/

Posts: 7772 | From Northeast, again... | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.