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Posted by kareamber (Member # 20110) on :
 
Well it's official... I was Dx'd today with Lyme Disease. The LLMD I saw was very confident in the dx.
It was so weird cause this morning before I left to the appt my regular GP nurse called me (totally out of the blue) and said that my dr wanted me to come in for a follow up.

I was a bit confused as the last time I spoke to my dr by phone she said she didn't my IgeneX tests revealed much but that she was going to look into it some more.

Well that was several weeks ago. I figured she just blew it off.

Well I guess she really was investigating it and researching it.

The nurse said she wants me to come in to discuss treatment options for lyme!

Anyways, my LLMD was going to give me abx there, but it would be free to get them from my GP at the base clinic.

So he sent a note with his recommendations for treatment. He recommended starting on 3 months of Cefuruxime.

I have a follow up with him in a month. After the three months of that we will re evalutate and change or modify abx and go from there...

He says from my WB it looks like I've had it a long time and recommends long term abx and possibly IV if the oral don't do well.

He also prescribed pro biotics and a high dose B12 even though I'm not deficient.

I have to go back next week for more labs: CD57, babesia, and ELISPOT from Germany. VERY EXPENSIVE, hopefully worth it...

I'm a bit overwhelmed and still in a bit of denial. I'm still having that "what if?" feeling.

I guess I'll just go ahead with treatment and see where that takes me. Take one day at a time.

Thank you all for your support and encouragment.

I really wouldn't be here today with a DX if it weren't for all your help. I'd still be wandering..


IGENEX IGG POS 30+ 31++++ 41++
IGM 30+ 31+++ 34IND 41IND 89-93IND

[ 07-09-2009, 11:45 AM: Message edited by: kareamber ]
 
Posted by Dekrator48 (Member # 18239) on :
 
Hi,

I am glad you are getting answers and starting treatment.

It is a long road so don't expect too much too soon.

Just keep reading, learning and posting!

All the best to you!
 
Posted by nenet (Member # 13174) on :
 
I know it's bizarre to say it and read it, but Congratulations on your diagnosis!

That is also great news that you will have a working partnership between your LLMD and your GP. That will help so much, as long as your GP will defer to the LLMD's larger knowledge base and wisdom when it comes to TBDs.

Were you evaluated for co-infections? It is the norm to have a co-infection or 3 when you have Lyme, so that's definitely something to be evaluated for, and to put into your long-term plans for treatment.

I understand the denial, we all do. I still have moments of it, 2 years after diagnosis, and even after seeing marked improvement after a year of antibiotics. The best remedy for that is reading scientific and medical literature on the disease and the microorganism itself. It really helps to read concrete science to soothe your doubts.

There are some great resources in easy-to-comprehend form in the 3rd link in my signature line.

Good luck kareamber! You are well on your way to getting better now!
 
Posted by ping (Member # 6974) on :
 
Welcome to our world. Wish I were welcoming you to a million dollar jackpot instead, but no such luck. You do have plenty of company here though. [hi]

Sounds like you got a good doctor. About all the tests... Quite frankly, I told my doc that I couldn't afford many of them and he understood and we ran them later down the line, as finances permitted. Up to you, but if you can't afford it, talk to him.

Glad to know you're getting some real help, kareamber. TTYL

ping
"We are more than containers for Lyme"
 
Posted by gemofnj (Member # 15551) on :
 
k

welcome. sorry you have lyme, but at least you had a positive test result!!

many folks have to treat without it. keep in mind that IND is considered a weak positive.

here is a sample photo of the bands. the dark ones have are represented by the most +'s :

http://www.igenex.com/lymeset2.htm

Igenex Western Blot Break Down by band

9 cross-reactive for Borrellia

12 specific for Bb

18 highly specific to Lyme (Many LLMD's say if this band alone is positive, you have lyme - see link above)

20 cross-reactive for Borrellia

21 unknown

22 specific for Bb, probably really the 23/25 band

23-25 outer surface protein C (OspC), specific for Bb

28 unknown

30 unknown; probably an outer surface protein; common in European and

one California strain - Has cross-reactivity with several different types of viruses

31 outer surface protein A (OspA), specific for Bb - Has cross-reactivity with several different types of viruses

34 outer surface protein B (Osp; specific for Bb

35 specific for Bb

37 specific for Bb

38 cross-reactive for Bb

39 is a major protein of Bb flagellin; specific for Bb

41 flagellin protein of all spirochetes; this is usually the first to appear after a spirochete infection but is NOT specific to Lyme (i.e, other spirochete diseases have flagellas - see link above "Western Blot Made Easy" for more info)

45 cross-reactive for all Borellia

50 cross-reactive for all Borrellia

55 cross-reactive for all Borrellia

57 cross-reactive for all Borrellia

58 unknown but may be a heat-shock Bb protein

60 cross reactive for all Borrellia

66 cross-reactive for all Borrelia, common in all bacteria

83 specific antigen for the Lyme bacterium, probably a cytoplasmic membrane

93 unknown, probably the same protein in band 83, just migrates differently in some patients[/b]

good luck and keep us posted [Smile]
 
Posted by kareamber (Member # 20110) on :
 
Thanks everyone,
Is there any particular supplements I should be taking along with abx? My dr didn't mention anything...
 
Posted by gemofnj (Member # 15551) on :
 
k,

you might want to check with your doctor on the supplements just in case he has his own recommendations.

however, taking a high quality/high culture refrigerated probiotic is essential while you are on antibiotics. this will help the body replace natural gut flora that is being destroyed by the antibiotics.

your doc may have a professional strength he recommends, or you can go to your local health food store and get one. it should be refrigerated.

im not sure what brands you have in OK, but something similar to Renew Life Ultimate Flora CRITICAL CARE is pretty good to start with.

This I have used it with good results and it is for people who are taking antibiotics.
http://www.renewlife.com/products/critical-care-50.aspx

someone else mentioned Dr. Hoffman's MD SELECT Advanced Probiotic.

just look for the refrigerated high quality/high strain.

Most lymies take multivitamins, extra b's, magnesium, immune support, and herbal antifungals to avoid getting yeast while on abx.

Here is copy of Dr. B's guidelines. May I suggest you read thru it to get a better understanding of diagnosis and treatment. You can print for future reference.
http://www.lymediseaseresource.com/BurrGuide2008.pdf

Lyme is complicated and there is alot to learn. Keep educated.

Good luck in your treatment and hope you feel better soon.
 
Posted by Lymetoo (Member # 743) on :
 
Highly positive test.. plus you have 83-93 .. the DNA of the Bb bacteria!

WELCOME to our world!!!! [Smile]
 
Posted by Dekrator48 (Member # 18239) on :
 
I take alot of supplements, but my LLMD says the 2 most important ones are:

1. high quality refrigerated probiotics with at least 50 billion cultures of strains beginning with "lacto" and "bifido".

2. Fish oil. I take 6 grams a day.
 
Posted by jennyflyer (Member # 12792) on :
 
I've found the probiotic that works best for me is Ultimate Flora Critical Care 50 Billion. Vitamine Shoppe and Vitacost usually have it on sale.
 
Posted by kareamber (Member # 20110) on :
 
Thank you so much for the help.
My dr already prescribed a probiotic... it is called Ther-Biotic COMPLETE from Klaire LABS. Anyone heard of this? It says 25+ Billion CFU's Multi-species. I have to keep in refrigerated.

The only other thing he prescribed was Pure encapsulations Methylcobalamin 1000 mcg. I guess its a high dose vit b12?

I'm gonna post this as a seperate question as well to get more feedback.

Thanks for you help again.
 
Posted by Tracy9 (Member # 7521) on :
 
Please feel free to join us also on www.lymefriends.com!
 
Posted by Pinelady (Member # 18524) on :
 
Good Job kareamber. Now to get well. These guys are right it is a long road, but very rewarding. Did he prescribe anything for yeast?
 
Posted by CD57 (Member # 11749) on :
 
Welcome!
How come your doctor ordered expensive tests from Germany? Curious.
 
Posted by kareamber (Member # 20110) on :
 
The tests from Germany are for the CD57, coinfections, and then the ELISPOT. I believe it is a specialty lab.

I have never heard of the ELISPOT until just recently. I guess it's another test, but is FAR MORE accurate than ELISA and WB.

It is only done in Germany. I don't have the website on me at the moment, but you can google ELISPOT lyme test.

I think it gives him a good idea of how bad the infection is and how long to treat. I think... i have a print off that explains it so I'll post later on it.

I'm still reluctant to BELIEVE or give in to this diagnosis. I don't know why either.

My symptoms, history, and WB all point to lyme. Do you all think my test results is a strong indicator of lyme???

IGG IGENEX POS 30+ 31++++ 41++ IGM 30+ 31+++ 34IND 41IND 83-93IND.

Still afraid it may be MS even though MRI's and tests have all been normal. Lyme is the ONLY test that has showed abnormal.

Thanks!
 
Posted by kareamber (Member # 20110) on :
 
CD57- I put a different post with the Elispot info...
 
Posted by kellyjk4 (Member # 19731) on :
 
Hi kareamber - I'm glad you have the diagnosis.

I too have a very positive test result and have questioned my diagnosis.

I think we get used to drs telling us that nothing is really wrong, or that we have something that is basically untreatable.

I was diagnosed with Fibroylgia, among other things, years ago.

It was when I began to fear that I had MS that I stumbled across information about Lyme Disease (thanks Dek - I'll always owe you).

At first, it seems almost worse to have Lyme Disease, since it's so hard for most people to get rid of it.

When you think about it though, the other diagnoses that people usually get instead are basically not treatable.

MS, for instance, is a horrible diagnosis. They tell you that you'll progressively just get worse.

Maybe you can slow it down, but you can't stop it and you just have live with it.

With Lyme, you have something to fight.

It's a long, hard road for most people, but at least you'll have your life back at the end of it!

It sounds like your dr is very knowledgeable - now you have to do your part and concentrate on getting better.

It's fantastic that your GP and LLMD can work together. That doesn't happen as often as it should.

I wish you the best of luck - keep us posted.
 


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