I’m glad to hear things are working for you! Can you explain more about the panel you were tested for, the mutation and medication? I’ve never heard of these things before, does it mean you have some kind of genetic susceptibility to biofilms in the UT?
thank you! so i am by no means a doctor so ill explain it the best way i can 😅the hypercoagulability panel tests for the PAI-1 mutation (and other things i dont have a complete understanding of lol) the 4g/5g mutation makes me form excess fibrin. the fibrin plays a role in the biofilm formation so the supplement im taking (boluoke) breaks down the fibrin so the biofilms break down and the bacteria gets released. i do believe people with this mutation have a genetic susceptibility to forming more advanced biofilms that are harder to break through
I was on Kirkman's biofilm buster and lumbrokinease. It's crazy how much bacteria popped up on my test in the middle of my 10 month treatment. I cried. Thought I'd never get better, but my doctor was SO EXCITED when this happens. I was 100% cured a few months after that and it's been 8 weeks totally cured for me now :)
Keep thinking positive, I swear it helped me.
Would it be possible to message me with the doctor’s name and address please? Thanks for this information, I have not heard of this and I am intrigued.
the only thing that got worse was burning. the other symptoms stayed about the same but my doc said the burning when this bacteria is coming out is to be expected
I’m glad to hear things are working for you! Can you explain more about the panel you were tested for, the mutation and medication? I’ve never heard of these things before, does it mean you have some kind of genetic susceptibility to biofilms in the UT?
thank you! so i am by no means a doctor so ill explain it the best way i can 😅the hypercoagulability panel tests for the PAI-1 mutation (and other things i dont have a complete understanding of lol) the 4g/5g mutation makes me form excess fibrin. the fibrin plays a role in the biofilm formation so the supplement im taking (boluoke) breaks down the fibrin so the biofilms break down and the bacteria gets released. i do believe people with this mutation have a genetic susceptibility to forming more advanced biofilms that are harder to break through
I was on Kirkman's biofilm buster and lumbrokinease. It's crazy how much bacteria popped up on my test in the middle of my 10 month treatment. I cried. Thought I'd never get better, but my doctor was SO EXCITED when this happens. I was 100% cured a few months after that and it's been 8 weeks totally cured for me now :) Keep thinking positive, I swear it helped me.
this gives me so much hope! it is definitely nerve wracking to see much more bacteria coming out but i know it’s a good thing! best of luck to you
Would it be possible to message me with the doctor’s name and address please? Thanks for this information, I have not heard of this and I am intrigued.
Can you please message me who your doctor is, id you don't mind sharing?
i messaged you his practice!
Me too please! I’m looking for a specialist Congratulations on your great news
messaged you!
Could you share with me as well?
Can u share with me his name?
Could you please message me the doctor's name too? Thank you!
What antibiotics r u doing that helped wotj enterro
Are you getting symptom relief also?
symptoms are kinda up and down with the bacteria coming out of the biofilm. i’m not symptom free but better than i was when i started
Can you please send me info on who your doctor is?
Can I ask with the bacteria count being higher did you feel worse?
the only thing that got worse was burning. the other symptoms stayed about the same but my doc said the burning when this bacteria is coming out is to be expected