Author Topic: Lyme Disease (Read 14911 times)

Muon · « **Reply #20 on:** December 10, 2019, 12:07:43 PM »

Could you ask for copies of your labdata b_jim and post it in the medical results thread?

demografx · « **Reply #21 on:** December 10, 2019, 01:54:35 PM »

Quote from: b_jim on December 09, 2019, 05:37:50 PM

Keep crossed fingers for me

b_jim · « **Reply #22 on:** December 12, 2019, 05:00:41 AM »

Thanks !
I will post my datas if it may helps some others. For the moment I have simply lyme Elisa and Western Blot tests positive. But it doesn't prove anything. It give me 25% to 50% to have Lyme disease.
Lyme disease is so complicated.

Several choices : we go to the antibiotic therapy : it may cure my lyme or not (and then polluate my liver/kidneys for nothing).
We wait and if lyme is real my symptoms will be worst....

Muon · « **Reply #23 on:** December 12, 2019, 12:19:16 PM »

Or you had an infection in the past and the body is still reacting while Borrelia is gone.

b_jim · « **Reply #24 on:** December 13, 2019, 12:27:07 PM »

My neurologist takes the decision quickly : antibiotic therapy now !
Maybe I had the disease in my veins but it woke up after excessive stress.

Eliasjoelrivera · « **Reply #25 on:** December 13, 2019, 12:41:43 PM »

Please keep informed about your progress. Maybe I can start treatment too.
Since entering the poiscenter site, I have taken nanna 1 treatments and also several others. They have been a lot of improvement for me. I have reduced the symptoms by half. I am also increasing my testosterone. Anyway, according to your results I will take this treatment for layme disease. I will consult with my doctor.

b_jim · « **Reply #26 on:** December 16, 2019, 10:29:25 AM »

I just learnt an important information 10 minutes ago !
Now, I'm 99% sure to have Lyme Disease.
And now I can say my Lyme started when my Pois started.
It is very possible that I never had Pois but Lyme.
Lyme was probably my Pois.

I don't say it is case for all other Pois sufferers. I only consider myself. Clearly some guys here has "hormonal Pois form" because they feel better with Testosterone, DHEA...

Now, what is this information ?
Erythema migrans is a 100% sure proof you have Lyme.
But according french professor Christian Perrone, Borrelial lymphocytoma of the earlobe is another 100% sure proof.

I get this at 15 years old more or less 6 months after my Pois start. Remember my Pois was gradual dispite lot of Poisers.

b_jim · « **Reply #27 on:** December 16, 2019, 10:45:14 AM »

Most of my blood exams are normal.
The important tests are
the ELISA (very positive 200++ [5-15] )
and WESTERN-BLOT ( 8++, 2+,6- )

I've started antibiotic therapy Ceftriaxone (Rocéphine®) 2000mg by injection (first was painful

now it's ok).

I want to use "natural antibiotic" to help a little more: garlic, thym.... but not "crazy remedies".

I want to add good food for microbiota : yoghurts, choucroute, olives, cornichons/pickles maybe tampeh and miso soup....

Nas · « **Reply #28 on:** December 16, 2019, 11:29:05 AM »

The woman POISer I talked to also had Lyme.

Muon · « **Reply #29 on:** December 16, 2019, 11:31:52 AM »

Lyme can activate mast cells.

Quote from: Nas on December 16, 2019, 11:29:05 AM

The woman POISer I talked to also had Lyme.

Which woman POISer?

Nas · « **Reply #30 on:** December 16, 2019, 12:59:05 PM »

Quote from: Muon on December 16, 2019, 11:31:52 AM

Lyme can activate mast cells.

Quote from: Nas on December 16, 2019, 11:29:05 AM
The woman POISer I talked to also had Lyme.
Which woman POISer?

I mentioned a year ago a woman having bad reactions to orgasm, I thought it was a big deal and you also commented on it.
Not surprisingly she also had a MCAS, in fact I met her in the MCAS group on FB.

Muon · « **Reply #31 on:** December 16, 2019, 01:39:49 PM »

Oh yes I do remember her. Totally forgot about it.

Hopeoneday · « **Reply #32 on:** December 17, 2019, 06:39:03 PM »

As i suspected, beacuse of we are immunocompromissed,
many of us might have layme disease and coinfections.

Lyme disiese usualy been follow coinfections like bartonela, babesia...
late chronic stages of this "bacteria" will be wery dificult to diagnose.

borrelia burgdorferi
https://www.google.com/search?client=firefox-b-d&ei=kmb5XbLeIojisAfxipaQAw&q=borrelia+burgdorferi&oq=boreliela&gs_l=psy-ab.1.1.0i13j0i13i10l2j0i13j0i13i10i30l6.200325.206144..209566...0.9..0.166.1304.1j9....2..0....1..gws-wiz.....0..0i71j0i273j0j0i10.YTsHRxUFi5Y
Borrelia burgdorferi is a bacterial species of the spirochete class of the genus Borrelia. B. burgdorferi exists in North America and Europe and until 2016 was the only known cause of Lyme disease in North America (Borrelia mayonii, found in the midwestern US, is also known to cause the disease).

Babesia

https://www.google.com/search?client=firefox-b-d&q=babesia

late chrinic stages of this parasite will be wery dificult to diagnose.
Obviously , here anti-parasiticsc could play a role.

Babesia is a tiny parasite that infects your red blood cells. Infection with Babesia is called babesiosis. The parasitic infection is usually transmitted by a tick bite. Babesiosis often occurs at the same time as Lyme disease. The tick that carries the Lyme bacteria can also be infected with the Babesia parasite.

Bartonela

https://www.google.com/search?client=firefox-b-d&q=bartonela

Bartonellosis is a group of emerging infectious diseases caused by bacteria belonging to the Bartonella genus. Bartonella includes at least 22 named species of bacteria that are mainly transmitted by carriers (vectors), including fleas, lice, or sandflies.

b_jim · « **Reply #33 on:** December 19, 2019, 12:18:17 PM »

Are we immunodepressed or lyme immunodepressed we ? Maybe both.

It's possible my bacteria stays under controle from 14 to 40 years old. After a severe stress, my immune system goes down and bacteria takes the controle.

Now I will try to kill it with antibios. But it"s not sure 100% of borrelias will be eliminated.
I need to have a good immunity and then less stress and good diet (no sugar no toxics and no acid foods)

Hopeoneday · « **Reply #34 on:** December 19, 2019, 05:25:48 PM »

Yes , thats why lyme and coinfection is hard to treat, we been infected because
we had bad imunity, then chronic lyme
supress ours imunity .
Yes it is posible to hawe infection more than 20 years.

Barba89 · « **Reply #35 on:** December 21, 2019, 11:29:44 AM »

Hi Guys,

it?s a pleasure to intervene on this post,
this morning I just did the lyme test (present and past infections),
I will update you as soon as I receive the results.
My pois doesn?t get better with taurine,
worsens strongly with the intake of dairy products and coffee.

Thanks for the shared info.

Regards

demografx · « **Reply #36 on:** December 21, 2019, 11:38:51 AM »

Barba89, best wishes!

b_jim · « **Reply #37 on:** December 21, 2019, 04:31:51 PM »

Quote from: Barba89 on December 21, 2019, 11:29:44 AM

Hi Guys,

it?s a pleasure to intervene on this post,
this morning I just did the lyme test (present and past infections),
I will update you as soon as I receive the results.
My pois doesn?t get better with taurine,
worsens strongly with the intake of dairy products and coffee.

Thanks for the shared info.

Regards

Hi. Do you have muscle twitching (fasciculations)?

Barba89 · « **Reply #38 on:** December 23, 2019, 12:27:53 PM »

yes,

only when i drink too coffee,
usually on my back.

b_jim · « **Reply #39 on:** December 23, 2019, 03:27:28 PM »

I sensible to coffee too. Magnesium and Vitamine D reduce my tremors.
Dairy products might unbalance calcium/magnesium levels for some people.
I stopped cow dairy products for now and I try goat/sheep cheese in moderate quantity.

News:

Author Topic: Lyme Disease (Read 14911 times)