posted
I know you will all say that there is no such thing as post lyme syndrome, but I would be grateful if you could give me some advise.
I have had 3 negative tests for lyme disease from the nhs & I really cannot afford to send a test to igenex.
I have seen several doctors due to ongoing symptoms (mostly neuro) following an infected blister on my ankle in Dec08 which could have been a tick bite. I was given 2 wks of penicillin for the infection, followed by 7 weeks of 200mg doxy as I convinced them it could be lyme.
They now think I have some sort of post infection syndrome, (I feel as if I have been plugged into an electrical current for the past 8 months), possibly caused by lyme and possibly but some other infection which has caused peripheral neuropathy.
I have been offered steroids as treatment but as I still have doubt that there my still be active lyme I have refused. The doctor is not prepared to issue any more abx.
I also have low white blood cell count. 6 months ago it was 2.5 but it has now risen to 3.
I know you would all recommend abx but as this is not an option, what treatment would you recommend. As far as I can see, the best option is to boost the immune system so that maybe it can fight the lyme it self.
I have an appointment with the consultant on 29th Sept and would like to be able to discuss some possible options for treatment that he may agree to.
Any Ideas
Posts: 69 | From UK | Registered: Jun 2009
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posted
You can try MP. It is very cheap. I dont see how can you "boost immune system" if you indeed have lyme , because BB is very powerfull immune suppressor by itself ( I bet one of the reasons some people dont show antibodies until a few month in treatment ). Also testing while on abx is not good if you want see antibodies
Posts: 856 | From MA | Registered: Jul 2009
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posted
Thanks for the reply coltman but what is MP? i've tried to google it but not worked it out.
My last test was in June when I was on abx, I'm going to try to get him to retest.
Posts: 69 | From UK | Registered: Jun 2009
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massman
Unregistered
posted
Tell the idiots that lyme is a CLINICAL DIAGNOSIS and NOT a lab diagnosis. This means that if you have some of the symptoms from the survey below you may have lyme.
ELISA followed by Western Blot is about 45% false negative. that means those tests, almost half the time, say you don't have it when you really DO !
69. Early on experienced a ``flu-like'' illness after which you have not since felt well
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Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Good call avoiding steroids. That can make this MUCH worse, unless life-threatening (and then you'd want abx protection with it).
---
It's not that you want to boost your immune system but bring it into balance. Simply put (because I don't get the full picture yet) the immune system has (at least) two parts: Th1 and Th2.
In lyme, one part is over-active and the other under-active. So, be very careful trying to "boost" anything. Support with Vitamin D3 (not D2) is a good idea, especially if you don't get much sun exposure on your skin (20 minutes a day).
--
Often, what some doctors call "post-infection" is really still infection that has not been properly treated.
Lyme tests are not perfect and, even 3, could be wrong. Lyme can go on for years - or a lifetime - if it is not handled adequately.
Also, there are other chronic stealth infections to consider, as well as other tick-borne infections.
I need to rest but will come back and see of others have added other information.
(Wow, I see you got several replies all the while it took me to type this one.) Also check out the NEWBIE thread at the top of Medical forum - by treepatrol.
Good luck. -
Posts: 48021 | From Tree House | Registered: Jul 2007
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posted
I can tick off loads of those symptoms, but as we know they can be caused by other things and my problem is convincing a doctor that relys on tests.
The one symptom I have that I have not managed to find with any other posible diagnosis is the clicking joints. All my joints click when I move, It sounds like someone snapping sticks. This seems to be specific to lyme.
Does anyone know of any other symptoms which might help convince him it could still be active lyme?
Posts: 69 | From UK | Registered: Jun 2009
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posted
That survey is mostly from Dr. B's information.
I would suggest getting rid of a doc that does not have the brains or the _alls to clinically diagnose.
Many of them use tests to not have to treat people, IME.
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WildCondor
Unregistered
posted
There is no such thing as post-Lyme syndrome, you are either cured, or not. Tell those ridiculous doctors to start educating themselves! Lyme is a CLINICAL diagnosis, you don't' need tests,
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Unless you have a history with this doctor, have an existing rapport, where you feel he's open to listening and invested in solving your health issues---
I wouldn't bother trying to convince him of anything. The average NHS md is as ignorant as the average physician here.
If you live remotely and aren't mobile, you may not have a choice in the matter.
Posts: 571 | From Massachusetts | Registered: Oct 2008
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posted
If you can't afford a $200 life saving test from Igenex, then I guess you'll have to live a life with Lyme.
Keep reading here so that I will feel hopeful that we can get through to you!
-------------------- --Lymetutu-- Opinions, not medical advice! Posts: 96222 | From Texas | Registered: Feb 2001
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sutherngrl
Frequent Contributor (1K+ posts)
Member # 16270
posted
I agree that Lyme is a "clinical diagnosis".
I disagree with Coltman, as I showed positive IGM bands 41 and 23 while on antibiotics. Did not show any bands before starting antibiotics.
Just my own opinion, but I don't believe you can kill spirochetes without antibiotic treatment.
Posts: 4035 | From Mississippi | Registered: Jul 2008
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posted
I have emailed Igenex for costs for tests. They have replied but not attached price list. I will try again.
Its not just the cost of the tests, as Igenex would not be recognised by the nhs, even if they did show positive it would not get me treatment.
I really need to try to get an nhs dr to take this seriously - thats why i'm preparing my case to take with me on 29th. I have already had 7 wks doxy, its not that they have not been at least partly supportive, even without a positive test.
I definately would not be able to afford private treatment, especially since it seems it would be for a long period of time.
I have only managed to find one LLMD in uk taking new patients and they are VERY expensive. This is why i'm trying to gather information to support my case for nhs treatment.
I am taking this seriously, but I am not entirely sure this is lyme. I don't think its right to take high dose abx if you're not sure. If only there was a reliable test.
I do understand there are many other people on this forum with the same problem & there is no easy answer.
Posts: 69 | From UK | Registered: Jun 2009
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massman
Unregistered
posted
on the survey - symptoms can come from other things BUT lots of these sympyoms together are a good indication.
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gemofnj
Frequent Contributor (1K+ posts)
Member # 15551
posted
even if you arent sure, the best way to treat is with abx.
most doctors agree its worth a try, at best your symptoms will be reduced, and then you will have the answer.
in other words, better to treat than not.
even after i had a positive test, i still second guessed the results. i am now in remission after a short 9 months of abx.
good luck to you. since my daughter lives there, as i understand the medical structure of the UK and their lack of lyme literate doctors.
Posts: 1127 | From atlantic city, nj | Registered: May 2008
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"ELISA followed by Western Blot is about 45% false negative. that means those tests, almost half the time, say you don't have it when you really DO !"
Posts: 207 | From NH | Registered: Jul 2009
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glm1111
Frequent Contributor (5K+ posts)
Member # 16556
posted
You might want to check out the parasite/worm threads. They can cause a lot of similiar symptoms to Lyme.
If you type in parasites and Lyme in the search bar you may be surprised. 90% of the population has parasites.
Gael
-------------------- PARASITES/WORMS ARE NOW RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS* Posts: 6418 | From philadelphia pa | Registered: Jul 2008
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TerryK
Frequent Contributor (5K+ posts)
Member # 8552
posted
If you absolutely can't get to a lyme literate doctor then the next best thing would be to try some alternative treatments and see if you get a response. Did you have a response to abx??
The dose of abx that they had you taking was not enough. 200 mg is bacteriostatic. Only keeps it from reproducing and not for long enough to get rid of the infection.
As others mentioned, co-infections must be addressed in order to be successful in treating lyme.
Read the Buhner book "Healing Lyme", The Cowden protocol etc.. There are lots of posts here at lymenet about alternative treatments.
Bottom line, after being bitten and treated by your doctors, you are still sick. If your doctors can't figure it out, and refuse to go further, then you have to do it yourself.
Don't buy into the many bogus diagnosis that are given out when the doctor can't figure out what is wrong. Chronic Fatigue syndrome, Fibromyalgia, MS etc. etc. All illnesses with unknown cause. No real treatment except pallative care. Your life can slip away while recieving no real help.
Wishing you the best, Terry I'm not a doctor
Posts: 6286 | From Oregon | Registered: Jan 2006
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massman
Unregistered
posted
Got that stat from this board. Remembered reading it here and posted to see if someone could give me the source.
Somebody did reply, I copied it for my PCP, a DO that has seen some lymies in CT. Not extensive work though. He thanked me but not sure if that was for true interest or politically correct.
Perhaps you could search for that reply to me. I was brain dead enough to not copy + keep it.
Checking for or treating for parasites is also a good idea. IME specific mixed herbals ( www.inno-vita.com ) work really well. One blend for large, another for small. Not sure if you can get them in UK.
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Vermont_Lymie
Frequent Contributor (1K+ posts)
Member # 9780
posted
quote:Originally posted by WildCondor: There is no such thing as post-Lyme syndrome, you are either cured, or not. Tell those ridiculous doctors to start educating themselves! Lyme is a CLINICAL diagnosis, you don't' need tests,
Exactly. You are going to have to make a decision, on whether to treat lyme by seeing a lyme literate doctor, or suffer the consequences of untreated lyme.
That is what it sounds like to me. I am not a doctor, just someone who suffered the consequences of untreated lyme for too long. Hope you can see a lyme literate doctor.
Posts: 2557 | From home | Registered: Aug 2006
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treepatrol
Honored Contributor (10K+ posts)
Member # 4117
posted
Your infected get a LLMd and save your life at least save yourself all the pain most of us have gone through. The national institutes of health not good.
-------------------- Do unto others as you would have them do unto you. Remember Iam not a Doctor Just someone struggling like you with Tick Borne Diseases.
METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628
posted
You need to convince yourself first that you are in-fact going in the right direction. You won't be willing to invest heavily financially (Nor go the distance to get the financial support) unless you know you have to.
That is why the $200 Igenex Western Blot is worthwhile. Lyme is a clinical diagnosis, but the problem that I've noticed is that some patients need to be convinced more so than doctors, else they bounce around for years listening to all the wrong people.
It's worth the money, because even if it's negative the probability is high it will convey some information that will help. Once you get a "whiff" that you're on the right track you can run other circumstantial testing, like Brain SPECT scans, and co-infection and various other testing through insurance supported labs. People who do have various bands show up are more inclined to invest in a Lyme Disease specialist, even if it means going into debt -- because the alternative is not pleasant.
-------------------- I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.
posted
I would like to thank everyone for their replys, I do understand your intention is to knock sense into me.
I think Metallic Blue has a good point, I am a very logical person, this illness is not logical and discisions are difficult.
My family is not convinced & neither are my doctors. This is a very difficult situation.
If they will not repeat the WB next week I will go ahead with an Igenex test. If they do I will wait & see the result first.
You are right, I am not convinced it is lyme - this is my problem. All I do know is I am not well and don't know why. I may possibly have been biten by something that may possibly have been a tick.
I go on this website when no one is in the house, just because they think im crazy.
I dont look ill, I just feel ill.
Posts: 69 | From UK | Registered: Jun 2009
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I always say we got the "Oh, but you look so good" disease.
-------------------- aka: Lyme Warrior
In order to do "real" science, you have to have a "real" conversation with nature.
Well Behaved Women Rarely Make History!
"Just Demand your Rights" Posts: 869 | From nor - cal | Registered: Apr 2008
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METALLlC BLUE
Frequent Contributor (1K+ posts)
Member # 6628
posted
quote: I would like to thank everyone for their replys, I do understand your intention is to knock sense into me.
I think Metallic Blue has a good point, I am a very logical person, this illness is not logical and discisions are difficult.
My family is not convinced & neither are my doctors. This is a very difficult situation.
If they will not repeat the WB next week I will go ahead with an Igenex test. If they do I will wait & see the result first.
You are right, I am not convinced it is lyme - this is my problem. All I do know is I am not well and don't know why. I may possibly have been biten by something that may possibly have been a tick.
I go on this website when no one is in the house, just because they think im crazy.
I dont look ill, I just feel ill.
And just be aware, some may try to convince you that the Igenex testing is invalid and lacks credibility. If you get a positive test result, it's not uncommon for physicians to claim "False Positive" Beware that this is 100% false. The lab is fully accredited, and has approval across many states, including the boards that determine license renewal after investigations that are conducted by interdependent organizations. All back-testing and comparisons have shown Igenex Western Blots to be highly accurate and sensitive -- but they're only accurate if the actual antibodies are in the blood sample. It's not any given labs fault if their test is 99% accurate, but that the samples which are in-fact coming from infected hosts lack the antibodies and thus come back negative.
So, be aware of that. The problem with Quest and Labcorp and many other commercial tests isn't accuracy, but sensitivity. Igenex is both sensitive and accurate but is still subject to negative results in immunocompromised individuals, especially those on steroids or who have been ill for many years.
-------------------- I am not a physician, so do your own research to confirm any ideas given and then speak with a health care provider you trust.
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