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 » HELP!! Son with bulls eye what dose of meds?

 - UBBFriend: Email this page to someone!    
Author Topic: HELP!! Son with bulls eye what dose of meds?
whatayear
LymeNet Contributor
Member # 15833

Icon 1 posted      Profile for whatayear     Send New Private Message       Edit/Delete Post   Reply With Quote 
My son was in a group where there were two tick


bites on other kids, i checked both my kids and


didnt find anything later a week later my son


had 2 bulls eyes on his back so off to the ER we


went, they put him on amoxy 250mg three times a


day. then we went to his peditrition yesterday


and she said 800mg twice a day. He is 5 and 59


pounds, what is the correct dose and length of


treatment for a child? My daughter is 2 and 24


pounds and has no bulls eye rashes but is


complaining of head and stomach pain on a daily


basis i have decided to treat her aswell becuase


this is just compleltly odd behavior for her,


she is has also been extremly cranky!!! and the


pediatrician agreed she couldnt find another


source for these new issues we have had with her


over the last two weeks she is giving her two


weeks of amoxy, agian she has NO bulls eye. Is


it best to treat her with out a bulls eye or


tick? They will both be tested in 3 weeks AGIAN


for comparison but after going through this


myself im thinking better safe then sorry,


right? I had neither a tick nor a rash and know


this is very common Please someone advise. thanks

[ 04-16-2009, 02:26 PM: Message edited by: whatayear ]

Posts: 229 | From front royal, VA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
John S
LymeNet Contributor
Member # 19756

Icon 1 posted      Profile for John S     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am not an expert and others here have way more information than me.

It saddens me that children are exposed to this.

I would treat both if I were you.

I think most likely they would be fine.

I am disgusted at the moment. Children shouldn't be put through this.

Posts: 743 | From New York | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
Geneal
Frequent Contributor (5K+ posts)
Member # 10375

Icon 1 posted      Profile for Geneal     Send New Private Message       Edit/Delete Post   Reply With Quote 
My children weigh 50lbs each.

One was just put on amoxi 800mg per teaspoon twice daily for an infection.

The math is easy to do.

However, I am not a nurse or a physician or anybody who can

Readily give advice regarding dosage.

Just wanted to share my children's dosage with you.

Hugs,

Geneal

Posts: 6250 | From Louisiana | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
nenet
Frequent Contributor (1K+ posts)
Member # 13174

Icon 1 posted      Profile for nenet     Send New Private Message       Edit/Delete Post   Reply With Quote 
whatayear, your kids need to be in treatment regardless of rash. And they need to get to an LLMD as soon a possible.


They could have more than just Lyme, in fact that is the norm to have coinfections! Just taking Doxy is not going to treat possible other infections.


Also, we can't tell you what the proper dose for your children is. You need to possibly call a LLMD Pediatrician and ask them to consult with your Ped until such time as you can get them in for an appt with an LLMD. There are other parents here who have done this.


ANYONE who is at risk for having contracted Lyme and/or coinfections needs to treat and needs to treat for FAR LONGER than the mainstream medical community understands. I believe ILADS suggests initial infection treatment for Lyme is about 3 months, but I could be mistaken. That does NOT include what treatment may be needed for other coinfections.


Time is of the essence! as I am sure you are aware as you have been here a while.


Just a helpful bit of advice, you will likely get more replies if you can break up your post (use the pencil edit function) so that those of us with Neuro-Lyme will be able to comprehend it. Sometimes people with late-stage Lyme cannot read large blocks of text.


Some people do better when you break your paragraph every 3 sentences or so. Just a suggestion. I had to skim your post for keywords as it was too much for me, and I think there are others here you might want to hear from who can't even manage to do that.


OH and please be advised that Lyme and coinfection testing is NOT to be used to make a diagnosis, and it is a clinical diagnosis that should be made by a specialist.


ALSO, testing for Lyme within the first 6 weeks will not be useful, as it looks for antibodies to Lyme, and they are not produced until AT LEAST 6 weeks after infection!

--------------------
Dr. C's Western Blot Explanation

Lymenet Success Stories

ILADS Treatment Guidelines

Medical & Scientific Literature on Lyme

"Long-Term Antibiotic Therapy Improves Persistent Symptoms Associated with Lyme Disease"

Posts: 1176 | From KY | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
disturbedme
Frequent Contributor (1K+ posts)
Member # 12346

Icon 1 posted      Profile for disturbedme   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
John, NO ONE should be put through this. [Frown]

--------------------
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 | Report this post to a Moderator
whatayear
LymeNet Contributor
Member # 15833

Icon 1 posted      Profile for whatayear     Send New Private Message       Edit/Delete Post   Reply With Quote 
Does anyone know of a llmd in VA for kids? I can NOT go to see dr jones i dont have the money!
thanks

Posts: 229 | From front royal, VA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
John S
LymeNet Contributor
Member # 19756

Icon 1 posted      Profile for John S     Send New Private Message       Edit/Delete Post   Reply With Quote 
I would start a new post with that subject, you'll get some hits.
Posts: 743 | From New York | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
whatayear
LymeNet Contributor
Member # 15833

Icon 1 posted      Profile for whatayear     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am so mad at myself I cant stand it, here

after everything ive been through I know about

lyme ive lived this hell and I was very carful

with my kids i honestly didnt let them go in the

grass as bad as that sounds. We just moved and I

wanted them to make new friends, we went to a

cook out two doors down and everyone said OH NO

TICKS ETC...and I let me kids play in a fenced

yard...and this is what i get I should have known

better...I just should have.. I am very good at treating

myself, I know my body and can listen to it and

have gotten myself out of this mess but I dont


know how to treat my kids or what do for cos etc

I feel lost and helpless just like i did when i

started this journey but worse becuase its my

kids I always said THANK GOD it was me and not

my kids and now here i am...

I am greatful that this has

been caught early and there was a bulls eye I and most

arent that lucky. I am very into treating natural

and the thought of having to dose them in ABX

makes me feel like an even bigger failure. I have


let not only myself but my kids down by not preventing

this from happening. Now instead of being a

family of 2 with lyme disease we are now a

family of 4 infected by lyme disease.

Posts: 229 | From front royal, VA | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

Icon 1 posted      Profile for Tracy9         Edit/Delete Post   Reply With Quote 
Morgan, it is NOT your fault. It is unnatural and unhealthy for children to never get to play outside. Most of us would not be afraid of a fenced in yard.

What you need to do is just spray them for ticks before they go outside and check them carefully before they go to bed each night. You know the drill. Have them shower or bathe if they've been outside, take off clothes immediately as they come in, and put them in wash.

They can't live in a bubble, you just have to take precautions.

For all you know a tick could have fallen off another child and landed on a seat your son sat down on next in school. There is no way to avoid them, none that I have found.

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
adamm
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Not sure what appropriate pediatric dosing is--maybe check Dr. B's guidelines.
IP: Logged | Report this post to a Moderator
Tracy9
Frequent Contributor (1K+ posts)
Member # 7521

Icon 1 posted      Profile for Tracy9         Edit/Delete Post   Reply With Quote 
I can tell you what my son is on, buy he is on different meds, and he weighs more than Jake. He is about 70 pounds, and takes Minocycline, Mepron, and Zithromax.....but is about to start on IV Rocephin.

--------------------
NO PM; CONTACT: [email protected]

13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG.

Posts: 4480 | From Northeastern Connecticut | Registered: Jun 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.