This is topic Tinnitus, floaters blurry vision and sever weakness? in forum Medical Questions at LymeNet Flash.


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Posted by terrirdls1 (Member # 9810) on :
 
anyone suffer from Tinnitus, blurry vision and sever weakness? I have had so many symptoms and not one dr. takes me serious when I tell them I think I have lymes. They seem to think Im crazy especially since we live in so. calif. Not lymes state. I finally had one dr. order a test and it came back negative. she almost threw it in my face. Im lost. I dont have anyone that would take me ceriously? anyone gone throught this and any suggestions to llmd in so. calif. I had the tinnitus for about 15 years now and it is in my right ear but every once in a while it shoots to the left and if the volume would stay I wuold shot myself. It is unberabble. But thank god it only happens once in a while for only seconds. The blurry vision has started 2 years ago and floaters. Dr. said it is part of getting older and I would have to deal with it. ????? I dont know anymore... help... terrirdl1 [confused]
 
Posted by bettyg (Member # 6147) on :
 
quote:
Originally posted by terrirdls1:

anyone suffer from Tinnitus, blurry vision and severe weakness?

I have had so many symptoms and not one dr. takes me serious when I tell them I think I have lymes.
(NO S ON LYME..)

They seem to think Im crazy especially since we live in so. calif.... Not lyme state.

I finally had one dr. order a test and it came back negative. she almost threw it in my face. Im lost .

I dont have anyone that would take me ceriously?

anyone gone throught this and any suggestions to llmd in so. calif.

I had the tinnitus for about 15 years now and it is in my right ear but every once in a while it shoots to the left and if the volume would stay; I wuold shot myself.

It is unberabble. But thank god it only happens once in a while for only seconds.

The blurry vision has started 2 years ago and floaters. Dr. said it is part of getting older and I would have to deal with it. ????? I dont know anymore... help... terrirdl1 [confused]

WELCOME NEWBIE! I will send you a PM, private message, with my 13 pages of newbie links/advise.

When you print off TREEPATROL'S NEWBIE LINKS I showed, look for THE SPOON THEORY..or PEOPLE SAY I LOOK WELL! Wonderful article for support!

you need a western blot IGM & IGG blood test done by Igenex, Calif. Read about it in Treepatrol's newbie links ... clickon his IGENEX link.
Bettyg [Big Grin]
 
Posted by groovy2 (Member # 6304) on :
 
Hi terri

Most people here have gone threw the same thing-

For me I got the run around lasted 18 yrs--
Doctors thought I was crazy--
--no one can be that sick

The tests for Lyme and co infections
are Very Poor- almost Useless--

False negitives are very common--
To many things can sque test results--

Lyme ect. should be dioanogonesed
by symptoms only--
at the moment this is the best way--

Most doctors have there head up there @ss --
and the sick paitents are the folks that
pay for there stupidity--


Ringing in ears is Very common
with these illenesses-

Floaters and vision problems very common too--

There are several good LLMDs in Cali--
Mine just moved to Frisco from Austn TX--
she is Real Good-- and really helped me-

Read DR B info in the Newbee pages--
its written in plain language and is a very
good place to start-- its 39 pages long
so print it out if you can--

You will get help here--Jay--
 
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