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 » UNEXPLAINED ITCHY BRUISES.. PLEAAASEE HELP!!!!

 - UBBFriend: Email this page to someone!    
Author Topic: UNEXPLAINED ITCHY BRUISES.. PLEAAASEE HELP!!!!
Koryn21
Junior Member
Member # 13926

Icon 4 posted      Profile for Koryn21     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi everyone..

Some of you may remember me or not.. I forgot

what other screen name I had.

I've been In remission from lyme disease for two years now. So for everyone out there that are suffering, Just know there actually IS a light at the end of th tunnel!!!

About the brusing... I had been itching my thigh for
More then a week now. And now I have 3 bruises In a row that are itchy.

At first the bruises weren't there.. My thigh near my knee was itchy for some weird reason and now I have 3 bruses in that same spot.

Could these possibly be a couple of bulls eye rash???

I haven't hit my leg or anything.. I've also been having symptoms like, extreme fatigue, massive mood swings, dizziness, Cold Intolerance and Loss of apetite.

I just want some Input from you guys... You all give very good advice.

Thank you all! I'm just wondering if this has happened to anyone else.

Its not in the "form" of a bulls eye rash, but just round bruises... its very weird.

Koryn

--------------------
~*In remission for 3 years!! There is a light at the end of the tunnel, just keep holding on!*~ Koryn

Posts: 8 | From Poke-A-Nose, PA | Registered: Nov 2007  |  IP: Logged | Report this post to a Moderator
cactus
Frequent Contributor (1K+ posts)
Member # 7347

Icon 1 posted      Profile for cactus     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Koryn - thank you for the remission hope!

If they are bruises, not rashes, could you have babs? ...either a relapse or a re-infection?

Easy bruising has been one of my "babsy" symptoms - along with the other symptoms you mentioned. Mostly noticed them along my thighs, and would have called them itchy, too - much more so than painful.

Just a thought...

Sending lots of hope that this is a bump on the road, and not an exit back onto the Lyme and co-infection highway,
Cactus

--------------------
�Did you ever stop to think, and forget to start again?� - A.A. Milne

Posts: 1987 | From No. VA | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
Koryn21
Junior Member
Member # 13926

Icon 1 posted      Profile for Koryn21     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for your advice.. I'm gonna have to go get tested again.

--------------------
~*In remission for 3 years!! There is a light at the end of the tunnel, just keep holding on!*~ Koryn

Posts: 8 | From Poke-A-Nose, PA | Registered: Nov 2007  |  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 
Hi Koryn!!! [hi]

I'm so sorry you've got problems again!! I was thinking babs too....the loss of appetite especially.

Check the pics of rashes here:

Treepatrol's links
http://flash.lymenet.org/ubb/Forum5/HTML/000569.html

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
CaliforniaLyme
Frequent Contributor (5K+ posts)
Member # 7136

Icon 1 posted      Profile for CaliforniaLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you have olive skin or African American skin or just not anglo-pink-white skin bulls-eye rashes CAN look like bruises!!
********************************************
Skin Color Can Hide Lyme Disease

By Julia McNamee Neenan
HealthScout Reporter
WEDNESDAY, Oct. 18

Blacks are about half as likely as whites to be diagnosed with Lyme disease,
perhaps because their darker skin masks the telltale rash that often signals
the disease, contends a new study.


As a result, blacks who do have Lyme disease are more likely to suffer from
arthritis and other serious manifestations that develop later, the researchers
believe.


The same likely holds true for Hispanics and other darker-skinned people,
experts speculate.


Carried by deer ticks, which infect people by biting them, Lyme disease
generally causes a rash, joint swelling, facial paralysis or tremors, fever and
fatigue early on. Longer term, it can lead to more serious heart, blood and
neurological problems. Between 1993 and 1997, 12,500 cases of Lyme disease were
diagnosed in the United States, according to the Centers for Disease Control
and Prevention.


The bull's-eye rash that usually first identifies Lyme disease in someone "can
be missed," says lead researcher Dr. Alan D. Fix, an assistant professor in the
epidemiology and preventive medicine department at the University of Maryland
School of Medicine. "It can certainly be ignored. But some later manifestations
cannot. If you have a big, swollen knee, you're going to seek help."


Whites long have shown higher rates of Lyme disease infection than blacks, Fix
says, but researchers have explained the difference with demographics,
believing that blacks were less likely to become infected because they
generally live in areas where few deer ticks are found.


"It has been attributed to the area of residence," Fix says, paraphrasing the
logic. "[People thought] this is a disease of the suburbs."


To test that theory, Fix chose to study a rural area in Maryland with a
relatively high incidence of Lyme disease and a black population of about 13
percent -- the state's upper Eastern Shore. Logically, he says, you should not
see much difference in the diagnosis of the disease bettween whites and blacks
in this area because both groups would have roughly equal contact with infected
ticks in daily activities near their homes.


Instead, he found that whites were 1.8 times as likely as blacks to be
diagnosed with the disease -- 42 whites for every 100,000 people, compared with
23.4 blacks.


And of those eventually diagnosed with the disease, whites were 5.7 times as
likely to have detected a bull's-eye rash, the study says.


When blacks who contracted the disease finally were diagnosed with it, it was
at a later stage of the disease, after other symptoms appeared, Fix says.
Blacks were 10 percent more likely to exhibit symptoms like neurological or
heart problems and 30 percent more likely to suffer from arthritis, he says.
Findings appear in the current issue of the American Journal of Epidemiology.


"The question is why," Fix says, adding that the only answers at this point are
speculation. "Is it because individuals aren't recognizing it? Or that if they
see it, they're not thinking much of it?"


Other possibilities, he says, may be that blacks simply do not have health-care
coverage that would allow for earlier diagnosis or that health-care
professionals may have interpreted previous statistics to mean that Lyme
disease is not a cause for common concern with black patients.


David Weld, executive director of the American Lyme Disease Foundation, says
the evidence suggests more education is needed. In the black population, he
agrees, Lyme disease "is underdiagnosed and underreported."


But the same problem exists in the Hispanic population, Weld says, because many
Hispanics also are darker-skinned, making it harder to spot the rash. That, in
turn, is compounded in the migrant worker population, which may have even less
access to medical care and also an aversion to government clinics, given that
many of the workers are illegal immigrants, Weld says.


Both Fix and Weld say there's some evidence that delayed treatment of Lyme
disease may lead to more problems in the long run. So, they say, failure to
diagnose early could mean greater damage for blacks.


Because the disease-bearing ticks often are as small as poppy seeds, making
them extremely difficult to detect, the rash is your best bet at a clear
diagnosis, Weld says. He estimates that it appears in 80 percent to 90 percent
of Lyme disease cases. --

--------------------
There is no wealth but life.
-John Ruskin

All truth goes through 3 stages: first it is ridiculed: then it is violently opposed: finally it is accepted as self evident. - Schopenhauer

Posts: 5639 | From Aptos CA USA | Registered: Apr 2005  |  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.