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Hyperthermia versus stem cells

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Posted 3/16/2019 8:15 PM (GMT 0)
Has anyone done hyperthermia chronic lyme? Looking into st. George Klinik in Germany. Have been on and off IV
Antibiotics since 1997 no longer responding so looking into this or stem
Cells. Welcome any feedback on hyperthermia or stem cells. I want to
Hear it all positive and negative so please comment. Thanks.
Posted 3/16/2019 9:57 PM (GMT 0)
Since 1997-wow. I would do both St George and stems.
If you haven't I would also get checked by a biological dds. Watch the move "Root Cause" on youtube
Posted 3/16/2019 10:56 PM (GMT 0)
Forum member Evanston took her daughter to Germany for hyperthermia.

Evanston”s daughter was doing really well the last time she posted - but the hyperthermia wasn’t as effective for herself.

She mentioned that the hyperthermia is good for lyme but not coinfections (that’s what they told her when she was there)

Re: stem cells - member 10LymeB went to a facility here in the US for stem cell treatment.

She had some improvement but not in remission. I think it was about a year ago that she went.
Posted 3/16/2019 11:01 PM (GMT 0)
Post by 10LymeB

https://www.healingwell.com/community/default.aspx?f=30&m=4113489
Posted 3/17/2019 1:57 AM (GMT 0)
Synergy is what I suggest.
Hyperthermia-stems and a good biological dds.
20 years of being sick I would throw the kitchen sink at it.
St Georges Clinic really helps some people. I know my doc was there three weeks ago training them
in some new techniques. My guess would be he taught them about dental and parasites.
Posted 3/17/2019 7:59 PM (GMT 0)
Hello.
I was at saint George in january 2018, in the same time than Evanston and her daughter.
Hyperthermia did nothing for me, a few weeks later my blood was loaded with spirochetes and my bartonella became much worse.
A scientist lymie friend think that hyperthermia can t hit the cyst form and the biofilms. And I think he is right.

Maybe if you have a strong immune system and no coinfection it can be good, but my immune system crashed right after the first round of heat and was way worse after this treatment. Before my cd57 were 47, now they are 12...
Just my experience.

Oh, and they say in the after hyperthermia protocole that they give us in the end that the hyperthermia doesn t work for people with bad HLA genes ( post lyme syndrom susceptible ). It would be nice if it was said before we go into this treatment ( I have a bad HLA).

Post Edited (Bullekideambule) : 3/17/2019 2:06:49 PM (GMT-6)

Posted 3/17/2019 8:03 PM (GMT 0)
Bullekideambule - I didn’t know that happened to you - or I forgot.... (which is quite possible)

That must have been very disappointing to travel there and spend the $$ - and not have some improvement.
Posted 3/17/2019 8:09 PM (GMT 0)
Oh, I am French so it was quite simple to go there ( in car, 12h).
But we had to sell pur house to pay this treatment and now I am bed ridden with horrible nerve pain and muscle spasms...
And no money of course.
Posted 3/17/2019 8:12 PM (GMT 0)

Bullekideambule said...
Oh, I am French so it was quite simple to go there ( in car, 12h).
But we had to sell pur house to pay this treatment and now I am bed ridden with horrible nerve pain and muscle spasms...
And no money of course.

Oh no! I’m so sorry!!

Are you able to afford herbal treatments? And self treat?
Posted 3/18/2019 1:23 AM (GMT 0)
So sorry for your long struggle. Its a long road. I think the key is to do as many things as you can to get better and create some synergy. I really almost never hear a person do one thing and regain their health.
Dental-parasite IV antibiotics, rbti,ozone sauna and stems have all helped. Dental-parasite have helped me the most.
There is a good movie on youtube-Root Cause"



Money is needed for all of this-sucks

Post Edited (magoo2) : 3/17/2019 7:27:20 PM (GMT-6)

Posted 3/18/2019 2:06 AM (GMT 0)
Something for you to try: Quercetin - it’s for mast cell activation syndrome.

Quercetin is a natural antihistamine

I don’t have any allergy type symptoms - ie skin issues, congestion etc - but I have nerve pain and shivers.

The Quercetin seems to be helping.

I tried many things for the nerve pain with no success.

I take two capsules at a time.
I think they’re 250 mg each
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