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» LymeNet Flash » Questions and Discussion » Medical Questions » Sun Increases Brain Fog - Anyone know why?

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Author Topic: Sun Increases Brain Fog - Anyone know why?
tom63376
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Anyone know why Sunlight increases
Brain Fog ?????

Posts: 57 | From St. Peters, Mo | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
daniella
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is it possibly from the heat...like a herx?

I know the sauna makes me foggy but then it clears after a while and then I feel better. I always thought it was a herx from the heat.


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tom63376
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If the Sun kills lyme and the result is
a herx reaction, Does that mean people
should get as much sun as possible so
that they clear more Lyme even though
it wipes them out?????

Posts: 57 | From St. Peters, Mo | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
Foggy
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I think itinflames the bb in the brain big time. I get so dazed from sun or oppressive heat.
Posts: 2451 | From Lyme Central | Registered: Aug 2001  |  IP: Logged | Report this post to a Moderator
tom63376
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Anyone have any tips that help
them tolerate the sun better so
we can enjoy nice summer days
outside without having our
heads explode from brain fog??

Posts: 57 | From St. Peters, Mo | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
Semper Fi
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If you are sensitive to the sun and lights, you may have a disregulated D 125 . This is one of the basis for the Marshall protocol. i was very sun and light sensitive, after 8 months or so it all went away and all of my symptoms. I'm on phase III and doing great.Check out marshall protocol.com. You can do the d tests and this is an indication of a d 125 problem. Also, if you are taking antibiotics like Doxy, or others, they make you very sun sensitive.Good luck
Posts: 512 | From Memlo Park, Ca USA | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
tom63376
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SemperFi-

I went to that website for Marshall protocol
and it's a little hard to understand. In
lay-man's terms what the heck is this?
Sounds like you get sick from vitimin D
and need to take everything out of your
diet that had vitimin D in it.. Is this
what they are saying. If so, many people
with Lyme may have it as well. How is it
treated? I mean come on you need Vitimin D
to live don't you? I have brain fog right
now so maybe I'm just overy stupid right
now...


Posts: 57 | From St. Peters, Mo | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
Lymeindunkirk
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this is an interesting question posted. Thinking about it I have always experienced extreme fatigue after being in the sun awhile. I believe I've been infected for at least 25 years. If it is true about maybe herxing that would be a good explanation for me. I try to stay out of the sun however as I am fair skinned and tend to burn easily. I always thought the fatigue I had after a nice day outside was from allergies. this has given me something to think about for sure.......
Posts: 547 | From Maryland | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
tom63376
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>Another possibility (educated speculation)
>is that heat and possibly sunlight causes
>borrelia organisms to convert from cyst
>forms to spirochete forms, and to "act up".
>Hence the worsening of symptoms.

Maybe Sun could cause them to act up but
I doubt heat does since a hot dry sauna
makes me feel great. (As long as I am
lying down while I'm in it)

I'd still like someone write about this
marshal protocol. From what I read
focuses around eliminating Vitimin D
from your diet. I can't figure out
how that would be a good thing to do..


Posts: 57 | From St. Peters, Mo | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
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quote:
Originally posted by tom63376:
[BMaybe Sun could cause them to act up but
I doubt heat does since a hot dry sauna
makes me feel great.

..[/B]


Spirochetes HATE the heat! I usually feel horrible in saunas or other hot places, for sure!! Many here use saunas as therapy.

The Marshall Protocol is a specific method of treatment for sarcoidosis. Some are now adapting this protocol for use against Lyme. It helps some, others not.

------------------
oops!
Lymetutu


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tickedntx
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Tom:

Read here for lay summaries/ explanations of the Marshall Protocol: http://www.marshallprotocol.com/forum2/364.html


Posts: 977 | From Austin, TX, USA | Registered: May 2004  |  IP: Logged | Report this post to a Moderator
Lyddie
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I've gotten really sick from sun exposure during my Lyme treatment (4 years). I had skin biopsy at one point, which indicated autoimmune activity in my skin, where I had ahd sun exposure.

I'm one of those people (as are my daughters) with the HLA DR4 genetic type, and I (we) have posoitive ANA's as well. As result, I have been diagnosed with "cutaneous lupus."

This is, however, in my opinion and our LLMD's, just another manifestation of my Lyme. In people with HLA-DR 4 type, Lyme triggers autoimmune activity, which may explain the fact that my Lyme is so hard to treat.

Have you had your ANA or HLA type tested? Just a thought...My situation is not rare at all...any LLMD should tell you that a positive ANA can accompany Lyme,and will go down with treartment at some point.


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