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Lyme Disease ForumsGeneral & SupportHas anyone been on A-BAB?
02/03/2011 11:00 AM
Cakeluva1980
 
Posts: 290
Member

Hello,

I searched and didn't find much on a-bab or at least the question I have about it.

My doctor believes the reason I can't get over the Lyme is because I have babesia I have all the symptoms but tests came up negative.

He said that the A -Bab (byron white formula) would help solidify his diagnosis. He said if I was not sick I would have no reaction.

Well I did have a reaction. I can't seem to get past 1 drop. It feels like my head is going to explode. That's my larget complaint. The stabbing pains which I had been getting in the past really intensified.

Has anyone else taken this? I'm not sure if this is a normal herx reaction or a closer to allergic reaction. I'm nervous because these are more than a little headache they progress to full blow migraines where I can barely walk.

Reply

02/03/2011 11:26 AM  Top
wlkthlne
wlkthlne  
Posts: 1608
Senior Member

I have spoken to some here, about the A-bab..it is strong stuff for them as well. I am on A-bart and I had to work myself slowly.

The HH did what you said the A-bab did to you, we switched to A-bart...not as bad..

There is a product bab-1 Bar-1 and Bb-1 that might be more less intence?

I took a Lyme tea...made with five of the herbs..because my Bart was so bad in my head...it would cause me to become blind in one eye for a minute or so.

As I have used other things to help with the Bart...I went back to the tea...just once in a blue moon...just to stir things up...see if I am missin' anything..

So far, no eye or head issues that where as bad as in the past...

So I am in hope...the different things are "git'in"

it..Smile

Good luck to you

wlkthlneCool

Anything I post or respond to comes from a Lyme and Bart victim himself. I am NOT a doctor. I do my own research for ME...I may share my findings and will post them. They are for general talk and vent...If a group leader feels the info is worth saving somewhere, they are more than welcome to do with it as they like. Wlk=)

02/03/2011 12:18 PM  Top
Cakeluva1980
 
Posts: 290
Member

It's strange for quite awhile my vision in my left eye comes and goes. It's really scary. I've had MRIs and my eyes checked while this was going on. The eye doctor said the eye itself is perfect. Sometimes I loose vision for a few minutes, sometimes a few hours quiet scary.

02/03/2011 01:54 PM  Top
wlkthlne
wlkthlne  
Posts: 1608
Senior Member

Cake1980, by no means am I a Doc...but now that you mention your eye problems and the other stuff..don't you think you should be treated for Bart!!!

Your symptoms seem to go more that route..do you have any issues with your feet?

Could you have Babs and Bart? If you do have Bart..you may have to get treated for that first...then the Babs?

Nothing is Cut and Dry with this crap...sorry...

What is your take on all this?

The Doxy/Rif combo..really ...really helped with my Bart eye symptoms!!! and now...finally the head pressure is getting much better..

My best to ya!

wlkthlneCool

Anything I post or respond to comes from a Lyme and Bart victim himself. I am NOT a doctor. I do my own research for ME...I may share my findings and will post them. They are for general talk and vent...If a group leader feels the info is worth saving somewhere, they are more than welcome to do with it as they like. Wlk=)

02/03/2011 05:48 PM  Top
Cakeluva1980
 
Posts: 290
Member

Yes, I have really bad cramping and pain with my feet. The doctor said that he thinks it's important to treat the babs first because I keep showing up as anemic and my blood pressure is dangerously low.

Ever since I started this treatment I feel so oxygen deprived again too. My only concern is that one of the herbs comes from a relative of a class of plant that i'm allergic too. That's why i'm afraid the reaction I'm having could be a slight allergic reaction.


02/03/2011 06:05 PM  Top
wlkthlne
wlkthlne  
Posts: 1608
Senior Member

Cake1980, think you just put the icing on the cake! If you have the feet issues as you said...You have Bart in my strong opinion...and I am sorry...

As for what the heck you treat first?????I would go with an LLMD...they(you would think) see and deal with this a whole lot.

Whew, you do have issues of concern and to address..

When I say I am sorry..what really goes through me is anger..not at you...this dane' Disease!

Grrrrrrrraahhhhhhhhh!Devil

May you get this under some control so you can fight all the demons....and get BETTER!

wlkthlneCool

Anything I post or respond to comes from a Lyme and Bart victim himself. I am NOT a doctor. I do my own research for ME...I may share my findings and will post them. They are for general talk and vent...If a group leader feels the info is worth saving somewhere, they are more than welcome to do with it as they like. Wlk=)

02/03/2011 07:37 PM  Top
Cakeluva1980
 
Posts: 290
Member

oh sorry it was my llmd that decided to try treating for babs first. I went and read the list of all the bart symptoms and I have every one of them. But he already told me I had it. He said the reason i'm not getting better was because my last doctor was missing a piece of the puzzle.

One symptom I have that drives me crazy that i've only seen mentioned here a few times is that I get these really strange pains on my scalp. It feels like my hair hurts. So I can never style my hair or else i'll be in pain until I wash it.


02/03/2011 07:45 PM  Top
VicMac
VicMac  
Posts: 1653
Senior Member

Unsure Cake, some really interesting information you are sharing here. If the ABab, did what you said, and the doc said it would help his diagnosis, then it does sound like you have Babs.

But WTL is right also, that your symptoms sound like Bart too. ( I am no doc either! ) But I hope you can find something that helps you with all of this.

ABab is another to put on my list. I think I have both Babs and Bart, and have been holding back the Babs with Artemisinin, that I have been taking for too long. I think my poor kidneys are getting weak.

But when I try to go off, some more really unpleasant head symtpoms come back.

But the more I hear about ABart And ABabs, this seems like a good way to go. I know what you mean about the strong reaction though. It is hard to tell if it is a herx or allergic reaction.

I have a question for you and everyone else about your foot pain. if you press into the bottom of your feet ( not real hard ), is it really painful then? It doesn't hurt me there, unless I do that.

And can you have terrible burning on the bottom of your feet too, that makes it hard to walk?

Cake I hope you get better, and keep us up on how you are progressing.

I wish I had solutions for everybody here who is suffering, but I am still hunting for them myself and seem to be more of a student on this board than a teacher. All I have to offer is my experience, support, and prayers based on what I have learned in my recovery. I am not a physician.

02/04/2011 06:30 AM  Top
wlkthlne
wlkthlne  
Posts: 1608
Senior Member

Vic and Cake...Vic, as for the foot stuff and Bart, many I talk to discribe it in different ways..It seems to me regardless of what or how ...it is IF you have symptoms..anykind..at your feet along with others..

Then it's writing on the wall..You got Bart!Sad sadly to say...

You guys got me looking some more, I could have swore that Bart needs to be treated! If not first..but along with everything else..

Not tring to quesion an LLMD here..but noticed they all have different views..Remember they are right along with us trying to treat something that is so off the page..

There is no Asprin fix here...for sure not cut and dry...

read this link! I never heard of these treatments for Bart..and what was written that Bart should be treated first....Umm..from what I am seein' the LLMD's are 50/50 on this..

perhaps it's what is effecting us the worst? That needs attention..well anyway..it's an open Book...Unsure

http://goodbyelyme.com/free-articles/coinfections/busting- bartonella

Good reading folks!

wlkthlneCool

Anything I post or respond to comes from a Lyme and Bart victim himself. I am NOT a doctor. I do my own research for ME...I may share my findings and will post them. They are for general talk and vent...If a group leader feels the info is worth saving somewhere, they are more than welcome to do with it as they like. Wlk=)

02/04/2011 08:31 AM  Top
VicMac
VicMac  
Posts: 1653
Senior Member

Wink Hey WTL, I feel like a squirrel. You keep giving me acorns ( or I suppose in our case ~~ cheese morsels ) that I absolutely have to go and stash in my diary!

Terrific article you contributed here!!! It explains a whole lot! And I never knew that Artemisia was also good for Bart!! Thats a first!

I have been taking the stuff for a year and half almost now, and have noticed that it has by far been the best natural I have taken for my head symptoms.

But, I have assumed it was only holding back Babesia!

Maybe this is more proof I have Bart??!!

I am trying to go off it again now, to give my kidneys a rest, and I have been feeling the return of some symptoms, including the burning pains on the insides of my arms and legs ( which your article describes also. )Very helpful.

Just to note: When I get the burning pains on the insides of my arms and legs, they always seem to parallel the lymph swelling that goes on in those regions too. There must be a connection.

I am having this now, since going off the Artemisia.

I really depend on that herb for these Bart symptoms! ( Or was that Bart Simpson? LOL ) Oh well.

Cake, you are right in that parts of the puzzle can be missing, and probably is when our treatment does not seem effective. Coinfections are to blame!

What I really want to find out, not just for my sake but all of ours on here -

is how damaging these herbs are to our liver and kidneys. The liver can regenerate itself, but the kidneys are harder to do that with.

I am worried about kidney damage, and also dont want to be careful suggesting these herbs to people if it definately causes that.

WTL, you are a gem in what you and some of the other Bart experts on here have educated us on!

Thanks for the cheese! And here's a big one for you today!!!

Wink Wink Smile

I wish I had solutions for everybody here who is suffering, but I am still hunting for them myself and seem to be more of a student on this board than a teacher. All I have to offer is my experience, support, and prayers based on what I have learned in my recovery. I am not a physician.
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