This is topic How many have crimson Crescent near tonsils area in forum Medical Questions at LymeNet Flash.


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Posted by Kerryblue (Member # 4077) on :
 
OK> Time to look...tee hee


Do you have prominent, what is called Crimson Crescents??

Suppossed to be indicitive of cfids/ME.

Also I have no gag reflex.
Used to gag really easy.

Sure could not be anorexic.>>>>
I can stick all my fingers down throat with not reaction.

Anyone else. I noticed this on another site. That is when I checked was surprised. Used to not beable to take vitamin without gagging.

Hmmmmmmm
 


Posted by Tincup (Member # 5829) on :
 
Good morning Kerry blue...

How do you do?

You said..

"I can stick all my fingers down throat with no reaction. Anyone else."

Sorry...

I am really not wanting to stick my fingers down your throat today...

But thanks for the offer...

I'm afraid the cost would be too great.

I would have to fly to Florida... rent a car.. drive to your place... and then there are meals, gas, and other expenses to consider too.

NOT that it doesn't sound fun and all... but...

Perhaps we can do it another time... ok?

You have neuro damage if you have no gag reflex... and have trouble swallowing. It can be reversed or improved by the way.

I had the same thing. My tongue is partly paralysed too... on one side.

You might want to see the post on cranial nerves.

The chiropractic neurologist was able to help with that situation.. very easily.

I also had the red marks you describe...

But they went away with proper antibiotic treatment.

Wanna see?

Well.. sorry I can't come down there today.

I am very busy.,

I gotta go lick all the snails off the bottom of the scummy pond....

If I didn't have to do that...

You KNOW I would come stick my fingers down your throat... and have a good old time doing it.


 


Posted by Kerryblue (Member # 4077) on :
 
You silly I meant I would stick my fingers down your throat.

I think the trip would be worth it. Don`t you miss Fl.

Alot of folks on immune board said they had the crimson cresents.

Someone posted big article on it being linked to Cfids./ME.

Also it was somebody who asked about the gag reflex. I never thought about it except can swallow bunch of Vitamoins. Never could do before.

You are too much~~~~~

I think yiu really need a Fl.vacation. May help that silly mind..lol..

No sleep last night again & have company coming in. Got to pull my act together here.
 


Posted by dullchime (Member # 6024) on :
 
Yeah I had the CC- they were more prominent when I first started to see signs of illness - now they are a lighter red color. what exactly is cfids??
 
Posted by dullchime (Member # 6024) on :
 
Are these crimson cresents something I should be worried about???
 
Posted by Kerryblue (Member # 4077) on :
 
According to long term research. Most people with cfids/Chronic Fatigue Symdrome/Now known a mylagicencephalitis.

This is disorder where overwhelming fatigue hits. No matter whether you sleep or not.

Fatigue that can actually hurt so bad.

It is not the best thing, just adds 1 more infection. Whether related to lyme or co-infect. Not sure. It doe`s have mortalitiy rate.

Cher was in bed 31/2 yrs. for it. Then she went ele natural. Said Sam-e helped her. SHe still suffers from it. Takes coach with trailor & big bed if she is trying to work.

You know she could have called God for help with her money. Still was in bed for 3 1/2 yr. It is known to go into remission all of sudden.

I just got med article yesterday. They proved gfids/ME. It is real, for the doubting doc`s.

Some are totally bedridden..
 


Posted by dullchime (Member # 6024) on :
 
My fatigue even with lyme disease hasnt been all that bad. Im starting to feel better with the doxy- but the fatigue was one of the first things that disappeared. Im still having my ups and downs of course, but I guess we'll just have to see.
thanks for all the info
 
Posted by dullchime (Member # 6024) on :
 
im confused, does this mean that its definitely not a lyme disease thing?? I dont know Im kinda worried now. I noticed the crimson the day i noticed I was feeling bad. 2months ago
 
Posted by dullchime (Member # 6024) on :
 
Ive read soo much on chronic fatigue-- how can any doc determine whether its CFS or lyme? The symptoms are near identical- If I didnt have the rash on my person- I would have been thinking thats what it was that I have. Anyway, this has been a day full of venting- I hope you can excuse me.

thanks for tha info
chime
 


Posted by Tincup (Member # 5829) on :
 
HA! You are a funny girl!!!

I was distracted while writing the reply yesterday and had to stop.. and wanted to add today....

There is a study... published yet??? .. or on the way?? Anyhow.. I heard of it last year.. from the doctor who did it..

They did biopsies on tonsils.

Over 20 of them if I recall.... after they were removed, of course.

ALL of them were found to have spirochetes in them.

Sooooooooo...

And keep in mind...

My cc's were there.. but were clear after proper treatment.

Hope this helps!

And yes.. I miss Florida. Especially since my "little one" is now there. He is helping with hurricane stuff on Sanibel Island.

Hope you got some sleep! AND enjoyed your company!!

Later gator...


 


Posted by dullchime (Member # 6024) on :
 
Tincup-- sometimes I think you are this websites personal Jesus- The worrying Ive been doing lately is the worst. Anxiety anxiety anxiety. Sometimes I can just read what you write and feel a thousand times better.

chime
 


Posted by suki444 (Member # 18960) on :
 
Hi
I know crimson crescents are supposed to be indicative of CFS in all the literature by CFS docs...but they are actually markers of when your Lyme is active according to Dr B.

I only developed permanent crimson crescents when my Lyme became full blown and they are always really noticeable now.

CFS/ME is Lyme.

BW
Emma
http://www.wendyslymefund.co.uk

 


Posted by lymiecanuck on :
 
Interesting post. I can swallow lots of pills at once now too, I thought it was all the practise, but now that I think of it i used to have a lot of problems taking one large vitamin without gagging.

Have to keep an eye on this. I don't know what crimson cresents are but my left tonsil has been enlarged since I had the worst case of tonsilitis ever about 6 months after being bit by lots of cat ticks, 15 years ago.

Interesting that they found bb in the tonsils, this is the side that gives me all the trouble. The left side of my head and the right side of my body. When sick, that side of throat always hurts more and that eye is the swollen one that barely ever goes down to normal size. When the ducks look in my throat, they always laugh to see how enlarged it, yeah, real funny...assh***s.

Tincup, you do have a talent to write great posts, I love reading them. Trout's pretty good too.
Lymiecanuck

[This message has been edited by lymiecanuck (edited 29 August 2004).]

[This message has been edited by lymiecanuck (edited 29 August 2004).]
 


Posted by trying2bsunny (Member # 5798) on :
 
I'm so glad to know I'm not crazy! I noticed this about 8 months ago after being told i didn't have lyme anymore but had developed chronic fatigue and possible lupus.

The nurse doesn't mind doing strep test on me at all. You could stick the swab clear down my throat and not even a flinch of a gag reflex.

My tonsils are also huge and a bright red to purple color. When i told this to my mom she thought i was crazy.

Now I have proof i'm not. Well... enough proof for me anyways!
 


Posted by lymiecanuck on :
 
Did the test....no gag reflex either.

Lymiecanuck
 


Posted by treepatrol (Member # 4117) on :
 
quote:
Originally posted by Kerryblue:
OK>
Do you have prominent, what is called Crimson Crescents??

Suppossed to be indicitive of cfids/ME.



Where exactly is this red or crimson crescents located ??

 


Posted by heckyeah (Member # 603) on :
 
quote:
Originally posted by Kerryblue:
Do you have prominent, what is called Crimson Crescents??

Yes. Both my fiance and I do and we both have Lyme... of course after being told we had CLASSIC CFIDS/ME (and me FM too) for many years.


Suppossed to be indicitive of cfids/ME.

Yeah... so they say. Not true though.


Also I have no gag reflex.
Used to gag really easy.

Before I finally got treated for Lyme I was dealing with dysphagia. My ability to swallow would almost totally disappear for days and I could barely swallow water without choking on it. If you lose your gag reflex I would assume it is somehow related to those same nerves. Thank God I got diagnosed and started treatment for Lyme and the co-infections.


Jen


------------------
Lilypie Baby Days).]

[This message has been edited by heckyeah (edited 30 August 2004).]
 


Posted by schamsjj (Member # 25792) on :
 
I have these and have had them since I got sick 7 months ago.

I have Lyme and Mycoplasma, My llmd said it indicates an active infection.

Im so tired of feeling like this. I am now going to try something called colostrum to see if that helps my immune system
 
Posted by jwall (Member # 22999) on :
 
Can someone explain what crimson crescents are?? My gag reflex is absent as well.
 
Posted by schamsjj (Member # 25792) on :
 
They are red crescents on each side of your throat.
 
Posted by randibear (Member # 11290) on :
 
my fatigue comes and goes. some days i just feel like a mack truck has run over me, other days not so bad.

this is sometimes so hard to figure out.
 
Posted by blinkie (Member # 14470) on :
 
I have them. They also get lighter with treatment but have never gone away. I ahve a lot of sore throats and a swollen gland on the right side.
 
Posted by Dawn in VA (Member # 9693) on :
 
Yep, count me in on the CCs.

As some of you may know, I used to work with human CFIDS serum samples under the scope, but even so, never myself got EBV or HHV6 until "the bite".

I also have an odd small "lump" near my right tonsil. I've asked my LLMDs about getting it removed for histology, but both have been rather ho-hum about it. Got it the same time as the CCs, right after tick bite #1(or 100?!).
 
Posted by mcg08002 (Member # 24617) on :
 
When I first got lyme, I had the WORST flu ever!!! Thats how my lyme started out, and since then, i have had a red crimson just like you described since last Nov lol. Docs always comment on it. Just means there is an active infection.
 


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