posted
the center (dark red) showed up a few weeks ago. now there is a "bullseye" around it. it's very small, though, smaller than a dime. the picture is a little washed out, the ring around it is actually very bright red.
Go to Seeking a Doctor and find a good LLMD in your area. Other docs are sub-par in abilities when it comes to lyme.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
| IP: Logged |
adamm
Unregistered
posted
It is. Don't even bother getting the horribly insensitive blood tests they run for the disease--you can be certain from that rash that you have Lyme.
That being established, here's what your doctor, for tragic reasons that are explained well on lymecryme.com as well as in a book by the title of Cure Unknown, doesn't know enough to tell you:
You now have an emergency on your hands. You must do whatever it takes to get enough doxycycline so that you can treat for 3 months with 400mg/day and then, for followup care, get to a doctor who treats in accordance with the guidelines of the ILADS (rather then the IDSA.) Failing to do this will, very likely result in lifelong illness.
IP: Logged |
feelfit
Frequent Contributor (1K+ posts)
Member # 12770
posted
Agree with Adamm.
That looks like a probable Bullseye to me. I would be asking for doxy pronto. Otherwise you may end up posting here for a long time down the road.
Not taking the abx will potentially hurt you more than taking them now even if that turns out to be a spider bite.
Feelfit
Posts: 3975 | From usa | Registered: Aug 2007
| IP: Logged |
posted
You should have a culture ran on that sore. It looks to me like it could possibly be MRSA, or a spider bite. If the hole continues to get bigger and have a yellow or greenish liquid discharge then it is probably MRSA or some other staph. I would have a culture ran on by your family doc for sure. Ive had Mrsa twice and it looks very similar to how it starts out. Starts like a pimple and then grows bigger.
Here is a pic to compare... looks just like it. MRSA
posted
Please go and get antibiotics. This disease can ruin your life. It has stolen my life as I knew it away from me, please go and get medicine asap. You still have a chance to not experience this.
-------------------- ~*~Lyme POW~*~
I will escape. Posts: 100 | From n/a | Registered: Oct 2008
| IP: Logged |
posted
I agree with hope. Defiantly go get this checked out.
Posts: 45 | From western kentucky | Registered: Oct 2008
| IP: Logged |
disturbedme
Frequent Contributor (1K+ posts)
Member # 12346
posted
I'd most likely say lyme, for sure.
If you could get a bigger picture of that rash, that would be better... for future purposes - like to show to your docs and insurance if that's ever needed, etc.
-------------------- One can never consent to creep when one feels an impulse to soar. ~ Helen Keller
My Lyme Story Posts: 2965 | From Land of Confusion (bitten in KS, moved to PA, now living in MD) | Registered: Jun 2007
| IP: Logged |
posted
even though it is so small? the rash is actually smaller than a dime. it seems like lyme rashes are huge. mine is tiny...
Posts: 12 | From georgia | Registered: Nov 2008
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
-
Sorry, I could not tell as the photo is so small.
However, I hope not but you should get it check out. take close-up photos along the way and be sure to keep for possible future use.
Here's a bunch of stuff to walk you through what to do if you suspect lyme. Treating early and aggressively (but while still not overwhelming your liver) is vital. Only a few doctors know how tod do this.
Oh, if this is not lyme and from an insect, you still need to know what is it and get appropriate treatment.
CONTROVERSY CONTINUES TO FUEL THE "LYME WAR" By Virginia Savely, RN, FNP-C
*****
As two medical societies battle over its diagnosis and treatment, Lyme disease remains a frequently missed illness. Here is how to spot and treat it.
Excerpts:
" . . .To treat Lyme disease for a comparable number of life cycles, treatment would need to last 30 weeks. . . ."
`` . . .Patients with Lyme disease almost always have negative results on standard blood screening tests and have no remarkable findings on physical exam, so they are frequently referred to mental-health professionals for evaluation.
"...If all cases were detected and treated in the early stages of Lyme disease, the debate over the diagnosis and treatment of late-stage disease would not be an issue, and devastating rheumatologic, neurologic, and cardiac complications could be avoided..."
. . . * Clinicians do not realize that the CDC has gone on record as saying the commercial Lyme tests are designed for epidemiologic rather than diagnostic purposes, and a diagnosis should be based on clinical presentation rather than serologic results.
- FULL ARTICLE AT LINK ABOVE.
Co-infections (other tick-borne infections or TBD - tick-borne disease) are not discussed in the Savely article due to space limits. Still, any LLMD you would see would know how to assess/treat if others are present.
==========================
AFTER reading the Savely article above this will make more sense and, sadly, shows the state of treatment:
Attorney General Richard Blumenthal today announced that his antitrust investigation has uncovered serious flaws in the Infectious Diseases Society of America's (IDSA) process for writing its 2006 Lyme disease guidelines and the IDSA has agreed to reassess them with the assistance of an outside arbiter.
You should also be evaluated for coinfections. Not all tests are great in that regard, either, but a good LLMD can evaluate you and then guide you in testing. One of the top labs is:
The International Lyme and Associated Diseases Society (ILADS) provides a forum for health science professionals to share their wealth of knowledge regarding the management of Lyme and associated diseases.
- 2/3 down the page, you can download Guidelines for the management of Lyme disease
posted
I have something that looks exactly like that on my thigh. I've had it for many years. Someone posted a picture a while ago that looked just like it and said that it was bartonella. I'll try to post a picture of mine in a few minutes.
-------------------- sunnymalibu Posts: 192 | From california | Registered: Jul 2006
| IP: Logged |
posted
I think I may have deleted the picture. If you do a search for bartonella pictures on this site you can probably see a picture that looks just like the one you posted. If not, check google for pictures of bartonella. Good luck!
-------------------- sunnymalibu Posts: 192 | From california | Registered: Jul 2006
| IP: Logged |
quote:Originally posted by doihavelym: [QB] even though it is so small? the rash is actually smaller than a dime. it seems like lyme rashes are huge. mine is tiny...
doesn't matter on size
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
| IP: Logged |
posted
I'll be the first to say it does NOT look at all like lyme disease. It's too small, is not a bullseye, seems to have a necrotic center...nothing about it is characteristic of lyme disease
Posts: 99 | From Bucks County, PA | Registered: Aug 2008
| IP: Logged |
posted
yeah theres no tick in it. i had my mom look at it with a magnifying glass.
the center looks like, a popped zit with dried blood on it... only its not a popped zit and its not dried blood. the center thing does not come off. the center thing is raised up a lot from my skin..
also it is VERY much "bullseye" shaped in real life. the center is darkred/black, then pink surrounding that, then a very blood red circle around all of it.
Posts: 12 | From georgia | Registered: Nov 2008
| IP: Logged |
gemofnj
Frequent Contributor (1K+ posts)
Member # 15551
posted
thanks for posting your photo, and as stated LARGER ones help us all better.
always use a coin or $1.00 bill to show size on you and TODAY'S DATED NEWSPAPER in visible spot for later references.
you've gotten wonderful advise from all of the above, here's my newbie info...
Welcome; i'm so glad you found us!! You've come to the right place for education and support!
Dr. Burrascano's most recent "Diagnostic Hints and Treatment Guidelines for Lyme and Other Tick Borne Illnesses" @ http://www.ilads.org/burrascano_0905.html suggests that you discuss with your doctor continuing treatment until you are symptom free for 2 months.
please see BettyG's newbie package info on the link below; click on link at bottom of my package. Check it out as time permits for you! @ http://tinyurl.com/58eyou
Fyi: we have over 1000 viewers daily; 200 - 400 posting/replying; so specific titles get our time/replies. non-specific ones, i sob, scroll on by!
Also, please be very specific in the subject line what you will be discussing so more people will be able to assist you.
***************
please go to my newbie links, copy the entire thing, and then print this off....
financial burdens compiled by melanie reber pages 74 - 92; outstanding info there.
also in my table of contents, for FINANCIAL BURDENS, i believe there are a few more general comments there without links!! print that off too as it's newer info from members thru their own personal, tragic experiences. thoughts and prayers headed your way..
POSTING GUIDELINES
When you post or reply, please break up your solid, continuous block text welcome to the board! many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.
please edit your post by CLICKING PAPER/PENCIL ICON to right of your name. that opens up BOTH subject line and body text.
now please break up your WORDY SENTENCES into one sentence paragraphs. Then hit ENTER KEY ``THREE`` after each paragraph; we need that space for comprehension.
if you are NOT a wordy person, you can do 2 or 3 total ok. do this for your entire post.
NOTE: you do NOT have to use "", just show the name of person you are responding to, and then type your comment.
IF you need to use "", PLEASE DELETE "BOLD" CODES so it's regular type text we read vs. the DARK, HARSH/PAINFUL BOLDING.
specifically, delete the first 4 characters of 2ND LINE of a ""
[QB] just delete these 4 characters, and BOLDING is GONE! my eyes will really appreciate that; it's one very bad side effect of my having lyme for 38.5 years!! xox
then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND
we thank you for helping us; otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me.
IP: Logged |
posted
i went to the doctor about the rash. my doctor told me i could go through lots of blood tests and everything, or she could just go ahead and put me on antibiotics. thoughts?
my rash is going away completely, is this normal? it is fading so much it is almost gone.
my rash pictures are linked on the first post on this topic, but now it is fading so much that is it almost gone.
Posts: 12 | From georgia | Registered: Nov 2008
| IP: Logged |
posted
i went to the doctor about the rash. my doctor told me i could go through lots of blood tests and everything, or she could just go ahead and put me on antibiotics. thoughts?
my rash is going away completely, is this normal? it is fading so much it is almost gone.
my rash pictures are linked on the first post on this topic, but now it is fading so much that is it almost gone.
Posts: 12 | From georgia | Registered: Nov 2008
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
-
Yes, a rash can fade. But, if it is lyme, the spirochetes can continue to do their work, or hide for a while.
While it's great that your doctor is willing to work with you, you need to find out more about what is being offered and her background and knowledge in the treatment of lyme.
You also need to be assessed for other TBD.
Most likely you'd get too low a dose of not the right combination and for too short of a time period. Did your doctor say which protocol she would use, the IDSA or the ILADS?
Not to insult or assault your doctor but most really just go by what the IDSA says. My guess is that she would treat with the IDSA protocol and that seriously inadequate (although a lucky few seem to have sailed through, many come back much worse later - see the Savely article in post above).
You can refer to earlier links for details. The ILADS site, Burrascano's guidelines and the Singleton book will be your very best resources to start.
It is never a single drug. Combination matters tremendously. This is very complex but well worth the attention to detail. It's your future, after all.
quote:Originally posted by doihavelym: i went to the doctor about the rash. my doctor told me i could go through lots of blood tests and everything, or she could just go ahead and put me on antibiotics. thoughts?
DO IT!!!! You don't want to go chronic like us!!!!
my rash is going away completely, is this normal? it is fading so much it is almost gone.
all the more reason to believe it's Lyme... they DO fade. Be sure to keep this picture!!!
I hope you got 4-6 wks of 300-400mg of doxy per day.
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
| IP: Logged |
posted
should i ask my doctor to give me more dosage and for longer? what should i ask for? (i cant go to any specialist or anything, just my regular ol doctor.)
Posts: 12 | From georgia | Registered: Nov 2008
| IP: Logged |
adamm
Unregistered
posted
Yes--ask around here for some research proving that it has to bee 400mg for about 3 months, then give it to your doctor and ask for it. If he/she won't give it to you, get it from a free clinic, another Lymie--anyone, and anyhow. A lyme support group, if there's one near you, may also be able to help you.
posted
ive continued my 200mg/day dosage because ive not had the time to contact my doctor.
i do plan on talking to her on monday and seeing if i can be put on a 400mg for 4 wks deal.
i woke up this morning with numb, tingly hands and a numb, tingly face. i have been experiencing some numbness in my left hand prior to this. i did do some drinking last night, but ive never experienced this from drinking before.
Posts: 12 | From georgia | Registered: Nov 2008
| IP: Logged |
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,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
![[Smile]](smile.gif)
welcome to the board! many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.![[Wink]](wink.gif)
otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me.
Printer-friendly view of this topic