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» LymeNet Flash » Questions and Discussion » Medical Questions » New Tick bite now blistered. Is this alarming?

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Author Topic: New Tick bite now blistered. Is this alarming?
LymeLearned
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Hi Everyone,
I arrived home Friday morning from a trip to the Ozarks with a tick in each ankle.

I'd been helping with some horses (I had not planned to be out), and went back in after a few minutes to put on pants, socks and shoes instead of my shorts and sandals.

This was on Wednesday and I found the first tick on Friday morning, (doc didn't even check the second foot, much less offer prophylactic treatment).

The ER doctor said to just wait to see if I develop symptoms. The second one was found on Saturday (48 and 72 hours embedded).

Thanks to God and all of you who write it out, I learned of what I needed & went to a Walgreens Clinic and got care that surpassed what the ER doc and even my own doc was willing to do.

The nurse practitioner gave me 200mg of Doxycycline Monday (yestereday) at 2:30 pm. She even knew what I needed before I asked!


Now, it's Tuesday and the 36 hour bite is blistered. Can anyone here ease my mind?

I SO want to scrape by with a close call and a lesson learned and nothing more. Any insights are greatly appreciated.

I'm so sorry I didn't know how to make this easier to read. [bonk]

[ 06-03-2009, 04:54 PM: Message edited by: LymeLearned ]

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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merrygirl
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WEll i would say that one dose of doxy isnt going to do much for you unfortuantely. You should be on at least 300mg doxy 2x a day for 4-6 weeks!!!
I would find a LLMD in seeking a doctor.

good luck. take pictures of the bites!!

melissa

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sixgoofykids
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Right, you should be on 200 mg. twice daily for 4-6 weeks. I would be concerned and would get treatment.

--------------------
sixgoofykids.blogspot.com

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Amanda
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take pictures, and make sure a doctor (or go back to nurse) sees the sore, and have them write that in your medical chart. that way, if you have problems later, you have some evidence.

You should find an LLMD and make appointment regardless. You need 4-6 weeks of 200mg doxy 2 x a day. Research shows that taking antibiotics for shorter time frames can cause you to come up negative on tests, but not whipe out the disease

Tuleremia (also transmitted by ticks) can cause a sore to develop around the tick bite area.

--------------------
"few things are harder to put up with than the annoyance of a good example" - Mark Twain

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adamm
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Nope--200 mg/day doesn absolutely nothign for Lyme. You need 400, and you should really continue with it for 3 months after all of your symptoms resolve. Do whatever it takes to get enough doxy such that you can do this, and then educate yourself about the disease and get to an LLMD. The CDC's been lying about this disease since day 1, so most docs know nothing about it.

lymecryme.com
lyme-info.net
lyme-rage.info
ilads.org
underourskin.com

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LymeLearned
LymeNet Contributor
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I feel like such an idiot! I'm a city girl who rushed out to get between my little daughter and a horse.

I rushed right back in to get covered up. I was SO ignorant! I had NO idea what a demon of a disease this is (corrupt science doesn't help).

I have pics of the embedded tick (both of them) and the blister as of today. A blister is bad? Please say no. Say it isn't so!

[ 06-05-2009, 12:18 AM: Message edited by: LymeLearned ]

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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bettyg
Unregistered


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welcome ll !

sorry, i couldn't read anythign you typed since i have severe neuro lyme. we need SHORT paragraphs and double spacing between each paragraph. could you edit your post please since majority of us here are NEURO folks? see my guidelines below ok [Smile] hugs


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 2008 Treatment Guidelines for Lyme and Other Tick Borne Illnesses" .
http://www.ilads.org/lyme_disease/treatment_guidelines.html


PAGES 17-19 discuss ADULT & KIDS MED TREATMENTS!
http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/80440?#000006
Dr. B's Supplement List
http://www.lymepa.org/Nutritional_Supplements.pdf


this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/77378

***************

TREEPATROL'S NEWBIE LEARNING LINKS ... over 1000 links of good info and guidelines galore!! MUST SKIM & READ !!

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/29917
************************************************************************


Betty's suggested POSTING GUIDELINES . 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 ``TWICE`` after each paragraph; we need that space for comprehension.

then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND

we thank you for helping us; [Wink] 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.
------------------------------------------------------

People seeking doctors might be able to get help from their state online information and support group. Nearly 3,400 people belong to state groups. Some of the groups are small but more than 20 of them have 50 or more people and seven have over 100.

To find your state group, go to
http://health.groups.yahoo.com/group/statenamelyme

Type your state name and lyme as one word, like this -
http://health.groups.yahoo.com/group/newyorklyme

South Carolina is the only state that needs a hyphen between the statename
and lyme, e.g. http://health.groups.yahoo.com/group/southcarolina-lyme

The groups are moderated and you have to apply. Most don't allow doctor names, but once on the group, you can ask for doctors in a certain area and ask people to email you privately.
*******************************************

This explains the medical politics around lyme WHY you need an ILADS-educated or ILADS-member LLMD (and there are also some ILADS-member LL NDs (naturopathic doctors):

www.clinicaladvisor.com/Controversy-continues-to-fuel-the-Lyme-War/article/117160/


TESTING

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:

www.igenex.com IGENEX

-----
There are a couple other good labs for certain tests: Fry; Clognen; Focus. Your LLMD will know.
========================

VERY important to read - even BEFORE testing:

Dr C's Western Blot explanation is discussed here:

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=042077

"With most infections, your immune system first forms IgM antibodies, then in about 2 to 4 weeks, you see IgG antibodies. In some infections, IgG antibodies may be detectable for years.

Because Borrelia burgdorferi is a chronic persistent infection that may last for decades, you would think patients with chronic symptoms would have positive IgG Western blots.

But actually, more IgM blots are positive in chronic borreliosis than IgG. Every time Borrelia burgdorferi reproduces itself, it may stimulate the immune system to form new IgM antibodies.

Some patients have both IgG and IgM blots positive. But if either the IgG or IgM blot is positive, overall it is a positive result.

Response to antibiotics is the same if either is positive, or both. Some antibodies against the borrelia are given more significance if they are IgG versus IgM, or vice versa.

Since this is a chronic persistent infection, this does not make a lot of sense to me. A newly formed Borrelia burgdorferi should have the same antigen parts as the previous bacteria that produced it.

But anyway, from my clinical experience, these borrelia associated bands usually predict a clinical change in symptoms with antibiotics, regardless of whether they are IgG or IgM."
===========

TREATMENT *** www.ilads.org

ILADS
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.

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LymeLearned
LymeNet Contributor
Member # 20565

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What a perfectly wonderful group you all are!!!

Know that you are saving one right now! Thank you

as if Thank you could ever be nearly enough!

I called the office of a doctor I learned of

through I-research, and I just hung up from his

nurse, who is shocked that nothing was done in

terms of testing or prophylactic treatment. This

office is willing and wanting to treat me

prophylactically --if only I can

manage to get an appointment. Wouldn't ya know it?

I'm not giving up. Thank you all for your

wonderful support and informative responses.

Sorry My earlier post was hard to read. Is this

correct? Again, I am deeply grateful. [Smile]

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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LymeLearned
LymeNet Contributor
Member # 20565

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Again, KNOW that I am deeply grateful for all of your help!

In honor of all of you, I have been telling everyone I know and some of the people I meet what you have taught me.


I also created a BLOG of my Tick experience called www.tickedoffliterally.blogspot.com

I detailed as much as I could of the things I NEVER knew before it happened to me (I drove 350 miles with a deer tick in each ankle). I OUTED the ISDA too.

At the bottom I added a much deserved thank you to the people of LymeNet, and a mention/promotion of the movie, "Under Our Skin".

My husband and I watched all of the trailers this weekend, and I cried. I can't *believe* this is America!

I will still feel like I won the lottery if I don't get sick. I will still be forever in your debt.

I will do my part to advance the cause the the awareness of Lyme Disease. You ALL have me forever!

I WILL see the movie. I will tell everyone I know to go too. I will bring tissue!

I am Grateful [bow] I am angry! [rant] ...that our government would DO this to the people! I LOVE every one of you for what you do! [kiss]

Please feel free to private message me if there's anything you want to share with me about my blog. My Warmest Regards!

[ 06-08-2009, 06:01 PM: Message edited by: LymeLearned ]

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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Lymetoo
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You came to the Ozarks and didn't give me a call!!???? I'm so insulted!!

Where did you go?

Ditto to your needing 400mg of doxy per day if you want to get well... and you DO!!!

PS... I'm in Missouri, not Texas.

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

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LymeLearned
LymeNet Contributor
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I went to Ellington....And my cousin's home, but Mom drove, so I can't remember the town! LOL

Um...All my doc was willing to give was 100mg tabs two teimes per day. IT took SO much just to get this far.

I'm tired (note as implied in my blog) that I wasn't in perfect health when I got bitten.

This could hurt me during any muscle ache/fatigue phases of Lyme(should they arise), as I have a spinal stenosis that is blamed for causing this in my legs for years. Yikes.

I think I'm stuck with the 200mg per day and Lotsa Prayer.

Isn't Missouri About the MOST beautiful thing you've ever SEEN???!??

I've seen every part of California, and it can't hold a candle to the peace and beauty of

Missouri. Only reason I'm careful how often I say this on the web or show pics is because I never want to see California'S fate (overcrowding and overpricing) visited upon anyone else.

Did ya see my blog? Did ya like it?? I hope SOMEONE reads it. I've never blogged before now, so I don't know how it all works out for people to find it. www.tickedoffliterally.blogspot.com

Actualy I did read 90 Minutes in Heaven! I've panicked when ever near trucks ever since. IN fact, I drove by night to MO so I would be among fewer on the road! Funny you should ask!

[ 06-08-2009, 06:05 PM: Message edited by: LymeLearned ]

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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LymeLearned
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OOPS I meant www.tickedoffliterally.blogspot.com

I was distracted by Don Piper talking to me in another tab!

Fascinating!

[ 06-08-2009, 06:03 PM: Message edited by: LymeLearned ]

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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Lymetoo
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heeehee... about the Don Piper!

Did you go to the Lake of the Ozarks?

I'm way south of there.

I'll check out your blog later.. not much into that myself. Thanks for inviting us! [Cool]

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

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LymeLearned
LymeNet Contributor
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I tried to make the blog loads of fun (my best friend laughed out several times while reading it with me on the phone)

...and I added stuff I think all of you would want the world to know. That's why I was hoping to hear from those in the know. [Smile]

I was in Ellington, Van Buren, Poplar Bluff, Sikeston and Cape Girardeau.

I LOVED Big Springs, PHotoraphed from the car window as we drove in the hills and from the back of a boat on Clearwater Lake.

I haven't yet been to Lake of the Ozarks, mostly because Mom's property is rignt on another lake.

My maternal side goes back many generations there. Mom is living in the house Grandma left her, and one day I will live there too.

--------------------
"SEVEN LYME FACTS THAT COULD HAVE SAVED ME" VISIT ME AT:

http://www.youtube.com/TickedOffLiterally

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