posted
Hi there - I'm new. Just got diagnosed a few weeks ago...
I've learned a whole lot already just reading these boards and also read "Coping With Lyme Disease".
Anyway, I'm wondering if anyone out there has ever tried combining Hyperbaric Oxygen treatments with any supposed cyst-busting drugs like Flagyl or Tinidazole? Wondering if that would help make the HBOT effects more "permanent"?
Thanks for any info!
KLP
Posts: 47 | From New York, NY | Registered: Jun 2005
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quote:Originally posted by KeyLymePie: Hi there - I'm new. Just got diagnosed a few weeks ago...
I've learned a whole lot already just reading these boards and also read "Coping With Lyme Disease".
Anyway, I'm wondering if anyone out there has ever tried combining Hyperbaric Oxygen treatments with any supposed cyst-busting drugs like Flagyl or Tinidazole? Wondering if that would help make the HBOT effects more "permanent"?
Thanks for any info!
KLP
Posts: 47 | From New York, NY | Registered: Jun 2005
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janet thomas
Frequent Contributor (1K+ posts)
Member # 7122
posted
I dunno, but anyone else??
Posts: 2001 | From NJ | Registered: Mar 2005
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posted
Seems like a good question, KeyLime. We've been looking at HBOT again, wondering if it might help my son with constant headache pain...in addition to everything else. Will be seeing our LLMD next week and will ask him what he thinks.
posted
Oh absolutely. I have done 130+ hyperbaric oxygen treatments, and a large majority of them were done while I was on Flagyl, along with IV antibiotics. I did HBOT twice daily, and my IV's an hour before each dive to ensure maximun potency in my blood. I also took flagyl before the dive, and oh boy did I herx!!! Its a very powerful and excellent combination. I did most of my HBOT treatments while on IV Zithromax, IM Bicillin, and oral Flagyl at high doses. Before and after each dive, I took really hot baths too!
posted
Thanks so much for responding!! I was going to ask you if you found that you were "cured" from this - but then I read your page. Wow. You had the most unbelievable struggle.
I hope and pray that you are steadily recovering from all of this...
Since some studies suggest that the HBOT treatments put the bug into a cyst state, I was hoping that taking a "cyst-buster" drug like Flagyl would make the HBO treatments truly bacteriocidal, and not just palliative.
So, I was hoping I'd achieve a lasting cure that way... but I guess that's too much to hope for right now.
My lyme, by comparison, is much less serious - so I thought I'd try a little "experimenting". The HBOT treatments are causing me to herx - and I've been doing some saunas too! (It really upsets the buggers)
Good luck with your recovery. Thanks again for responding.
KLP
quote:Originally posted by WildCondor: Oh absolutely. I have done 130+ hyperbaric oxygen treatments, and a large majority of them were done while I was on Flagyl, along with IV antibiotics. I did HBOT twice daily, and my IV's an hour before each dive to ensure maximun potency in my blood. I also took flagyl before the dive, and oh boy did I herx!!! Its a very powerful and excellent combination. I did most of my HBOT treatments while on IV Zithromax, IM Bicillin, and oral Flagyl at high doses. Before and after each dive, I took really hot baths too!
Posts: 47 | From New York, NY | Registered: Jun 2005
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posted
KLP, Where are you doing the treatments and are they at 2.4 ata or the milder form? Do you always herx after each treatment or are there some palliative effects?...appreciate the info. Hope you can get the upper hand quickly and feel better soon.
posted
I'm doing it at a clinic in Mahopac, NY. I wanted to start out immediately at 2.4 ata, but they wouldn't let me. And it was a good thing too! I herxed sooo bad at 1.4 ata, thought I would explode...
We are going down slowly to 2.4 ata over several sessions. So far I've had 5 treatments, making it down to 1.6 ata, but had to come back up due to some pain in my sinuses.
So far, have not had serious relief, just herxing, although my sleep is slightly better... so we'll see.
thanks for the good wishes.
KLP
[This message has been edited by KeyLymePie (edited 08 June 2005).]
Posts: 47 | From New York, NY | Registered: Jun 2005
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WildCondor
Unregistered
posted
KeyLimePie, can you email me please, I'd like to talk to you about HBO and Lyme. Thanks! My email is [email protected] I have some tips for you!
quote:Originally posted by KeyLymePie: Since some studies suggest that the HBOT treatments put the bug into a cyst state...
I've heard people guess and speculate about that, but nobody can actually produce the studies. That's just one of those rumors that gets passed along IMO.
Posts: 600 | From Las Vegas, NV | Registered: Nov 2004
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oxygenbabe
Frequent Contributor (1K+ posts)
Member # 5831
posted
HBOT is great and can make a big difference. There is an RN in New Jersey, she and hub got bad lyme landscaping their place, were misdiagnosed etc. Finally did 3 mos IV rocephin then she trained at an hbo clinic and bought herself a used secrets (monochamber) and treats herself and husband every other day. THey are fine. She is treating another lymie who was basically totally disabled even in spite of abx, and he is off abx and doing well. I was out there the other day getting a session while my own home chamber is out for repair.
It does not eradicate all of the spirochete, though probably nothing does. There's no proof of what state it puts the spirochete in, there's so much speculation about cysts etc but no in vivo studies to prove what makes a cyst and what doesn't.
Probably there is no special abx for use with hbo, it depends on what you've got and your strain
In re: babesia, a doctor who has lyme and babesia tested her blood before and after hbo sessions, and at 2.4 it kills babesia.
Posts: 2276 | From united states | Registered: Jun 2004
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Dr. Fife's research suggests going to 2.36ATA (45fsw) for effective treatment but he also recommends 30-60 treatments. WOW $$$$$$$$. You mentioned 1.6 ATA. At 19.8fsw you might as well sit at home in a recliner with a cylinder of O2 and watch a movie! 1 ATA is surface so 1.6 ATA is practically useless.
Because HBO is an fairly new and experimental treatment for lyme, there is no research yet as to the long term effects.
I have access to an incredible chamber and I haven't done any HBO yet (except as a tender but I am not breathing 100% O2. It is SO expensive, insurance won't cover it because it is not one of the recognized treatment areas for HBO and I haven't seen any evidence that it is effective long term. Even Dr. Fife says it is only an adjunctive therapy.
Oxygen is a wonderful drug. It helps lots of different things. If it makes people feel better--great--but you may get the same effects on surface Oxygen and it wouldn't break the bank.
I don't mean to sound negative. I have researched lots of things and because I have access to HBO, that was one of my first thoughts but the research is not convincing as of yet. Even Chico Hyperbarics says "most subjects began to show major improvement that in SOME instances has continued for 8 months." I guess it is up to the individual whether the benefit outweighs the cost.
The monoplace chaber mentioned is a Seachrist chamber. If you have one at home, make sure there is someone qualified to oversee the treatment. If you want pictures of chamber fires and explosions (remember we are dealing with 100%O2)let me know.
Good luck! Be sure and keep us posted if it is more than a temporary improvement. I would LOVE to change my mind about HBO and Lyme.
divemedic
Posts: 11 | From North Carolina | Registered: Mar 2005
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posted
My experience with hbot has been 20 sessions only. I started them when I was told (and believed) I had MS. Sessions ended knowing I had Lyme. I haven't been back in 6 weeks.
What you're asking KeyLymePie makes sense. To take abx while doing hbot. I stopped hbot since abx to recover (even slightly)from the herx.
Indeed, I felt awful. I'm still not recovered from it. I don't know if I will anytime soon. See, there was the travel to the hbot place (stress) as well as the actual dives.
WildCondor, I am still wiping some tears from reading your story. WOW! Good for you for preservering. You will make it. I pray you'll feel better really soon.
Let us known what you decide. Either way, all the best to you!
Posts: 371 | From Up North | Registered: May 2005
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I've heard has worked very well for some, and not at all for others..others became worse.
So, I also think it shouldn't be considered across the board reliable, yet at the same time is a viable alternative therapy. Treatment for TBD's is highly individualized.
I think the co-infection Babesia may be something to look out for with this treatment. Perhaps success has to do with timing, state of infection(s), prior therapies and concurrant therapies.
I bet, as with anything else, it's safe to say that you need to read all reported info you can and monitor your individual responses very closely no matter what you use.
I believe M.Hoggard at Chico in CA knows much about Flagyl and HBOT, maybe he could help. (?)
There are as many treatments as there are patients it seems sometimes! Just keep blazing your own trail.
All the best, Mo
Posts: 8337 | From the other shore | Registered: Jul 2002
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