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» LymeNet Flash » Questions and Discussion » Medical Questions » droopy eyelids better on cowden!!

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Author Topic: droopy eyelids better on cowden!!
randibear
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i have had really bad dropping eyelids for at least a year and longer. i would get up in the morning and they would sag into the eye. they stayed constantly irritated and puffy.

since i have been on cowden, now for about a week, i have noticed that when i get up in the morning my eyes do not look nearly as bad. in fact i look awake!!!

i don't know what's happening but the eyelid appears to be lifting.

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do not look back when the only course is forward

Posts: 12262 | From texas | Registered: Mar 2007  |  IP: Logged | Report this post to a Moderator
massman
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Good to hear !
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Rumigirl
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Wow, that's encouraging! I have the same problem. Keep us posted as to your progress with it. It didn't happen to me on the Cowden Protocol, but I only was on it for a few months or so.
Posts: 3771 | From around | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
psr1
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This also happened with me. I have been on Cowden for about one month. Did the Cowden protocol get anybody well?
Posts: 360 | From New York | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
Marnie
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Droopy eyelids?!

http://www.mayoclinic.com/health/myasthenia-gravis/DS00375

I personally know someone who at the age of 17 got MG.

He had his thymus gland removed at Northwestern Hospital and totally RECOVERED.

The thymus gland is where our defense cells go to become T cells.

Now he has to take a LITTLE steroids the rest of his life, but he was CURED.

Whatever pathogen he encountered (likely at a 5 star dude ranch his family went to) hit him very fast.

MG is extremely rare in young people.

I WONDER if removing the thymus gland would help cure lyme disease too.

Halt T cell production?

Posts: 9424 | From Sunshine State | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
MY3BOYS
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droopy eyelid sent off bell here too.... have you been tested for Myasthenia Gravis ????

randi=-=- think i may recall ( MAY being operative word...lyme brain and all).. havent you have problems resonding to antibiotics, etc?? lyme treatments????

anyway, the test is labs for anit-acetylcholine antibodies... may be worth looking up.

actually, i am waiting on test results for same but bc of very, very odd response had to increased acetycholine in brain. neruo doesnt think is the issue. we will see !!!

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i am not a Dr. any info is only for education, suggestion or to think/research. please do not mis-intuprest as diagnostic or prescriptive, only trying to help. **

dx in 08:lyme, rmsf, bart, babs, and m.pneumonia.

Posts: 422 | From TX | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
   

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