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» LymeNet Flash » Questions and Discussion » Medical Questions » HPMP anyone??!! (working for me)

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Author Topic: HPMP anyone??!! (working for me)
Guilford CT-lymer
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It's been a while since I posted here. I don't even remember my last user name (slymer??- any ways it stopped working & never was fixed).

I'm curious if any one has tried the HPMP outlined in the Rosner book- and how their results are. I got one and use it almost every night for 1-2 hours. When I first got it I ran it from 12v & immediately had herxing- deep body aches, headaches, etc. Since over around 2 months or so this has diminished so I increased to 24v this past weekend & it's kicking me in the pants- more achy, more headaches, weird spacey/ floaty feeling.

I have to say that the HPMP has helped me immensely. I will add that I'm on antibx & herbals- but they seemed to slow drastically in their effectiveness. At my worse I could not go in a public place due to anxiety, had to nap every day for 2-4 hours, extreme brain fog & was wishing all the time I would die- all the good stuff. Now I have a few weird brain/ floaty feeling, all over neuropathy, all over burning/ pins & needles, body aches------but I'm able to function almost normally, work out 5 days a week, fulfill by role as husband, dad, homeowner and architect-----sometimes it's tough.

I'll also add that last check my CD57 was 330 so my LLMD thinks my issue is either babs or barts-------which I told to my useless doctor when all this mess started.

So - back to my main reason for posting.....anyone HPMP???

Posts: 11 | From Guilford, CT | Registered: Aug 2010  |  IP: Logged | Report this post to a Moderator
Keebler
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For reference to those new to all this: HPMP is the High Power Magnetic Pulser, described in book below (and also possibly at YouTube with a cross search with Rosner).

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Glad to hear you are doing so well. Regarding the neuropathy, were you able to use liver support during your HPMP treatments?

Now, are you still taking magnesium and fish oil? A medicinal mushroom called "Lion's Mane" - and Gotu Kola - can also help but it can take a long time to recover from neuropathy.

Since you are using a new frequency, it may have been just too much all at once.

I am not familiar with the HPMP, however, with rife, treating only every 12 days is vital and keeping the time down to a few minutes before gradually increasing but still, no more than every 12 days until quite a ways into it. More than that can damage the liver and kidneys, and could cause neuropathy, too. The HPMP may work similarly.

Corydalis can help reduce pain in nerves.

So can Saint Johns Wort but a homeopathic form of that can work better for nerve pain than the actual herbal supplement.

You might post this question at the Rife thread below.

========================

http://www.lymebook.com/lyme-disease-rife-machines-bryan-rosner

Book: Lyme Disease and Rife Machines by Bryan Rosner

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http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/88778

RIFE Support Discussion Thread

=======================

Check your meds and supplements regarding how they use/stress the liver detox pathway, Cytochrome P-450 as that can cause neuropathy when it's overloaded:

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/91842?

PORPHYRIA Thread - along with details about KPU/HPU (Mauve factor)
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Guilford CT-lymer
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Hi Keebler!

To address your questions/ statements:

1. I have been taking 1,200 mg Milk Thistle 2x daily for liver support. Also my naturopath check my liver w/ his VEGA machine once a month and my LLMD checks a complete blood test every 3 weeks........my liver has been stellar since day one (I guess it recovered from college- just kidding).
2. I take 300mg Magnesium 2x daily....no fish oil currently.
3. I should clarify- the neuropathy began a few months before I started the HPMP. It started when I began Minocycliene & Rifampin. It was much worse in the beginning and gradually tampering off.
4. The HPMP is not actually a frequency....it's a radiant magnetic pulsed field (I use it in contact too).
5. In corresponding directly with Robb Alan- it sounded like when he was treating he used the HPMP everyday- changing some of the settings.

Thank you for the input.

Posts: 11 | From Guilford, CT | Registered: Aug 2010  |  IP: Logged | Report this post to a Moderator
Keebler
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thanks for the reply. I have to space this out to read it:

Guilford writes: To address your questions/ statements:

1. I have been taking 1,200 mg Milk Thistle 2x daily for liver support. Also my naturopath check my liver w/ his VEGA machine once a month and my LLMD checks a complete blood test every 3 weeks

........my liver has been stellar since day one (I guess it recovered from college- just kidding).

2. I take 300mg Magnesium 2x daily....no fish oil currently.

3. I should clarify- the neuropathy began a few months before I started the HPMP. It started when I began Minocycliene & Rifampin. It was much worse in the beginning and gradually tampering off.

4. The HPMP is not actually a frequency....it's a radiant magnetic pulsed field (I use it in contact too).

5. In corresponding directly with Robb Alan- it sounded like when he was treating he used the HPMP everyday- changing some of the settings.

Thank you for the input.

(Guilford)
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Keebler
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Oh, good to hear "the neuropathy began a few months before I started the HPMP"

I thought it happened afterward. Glad that is not the case.

Sounds like you are on board, then, and you were simply stating:

"increased to 24v this past weekend & it's kicking me in the pants- more achy, more headaches, weird spacey/ floaty feeling."

Hope that gets better. The magnesium dose may be too low (you can go up to bowel tolerance and back down. I take 1,000 a day, sometimes more). More magnesium should help decrease the reactions you're having right now.

Adding fish oil (such as OmegaBrite) will likely help tremendously, too. How are you getting all your fatty acids, though? Some other sources?

I see now that you are basically wanting to know if other used HPMP to compare experiences. I hope you posted over at the Rife thread as you are more likely to get replies there about this.
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Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
   

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