Yolanda Foster and her children doing LDI

www.people.com/article/yolanda-foster-bella-anwar-hadid-lyme-disease

Yolanda posted photo of her and kids LDI. I have the same one in my fridge using same doctor. Just took my bartonella only dose yesterday, no improvement yet. I am at a much lower dose (lower number is more concentrated in LDI) than Yolanda and kids. I started at 16, she is at 10. The cool thing is that IF this works I can use it to figure out what coinfections I have. So if I get improvement doing just Bartonella, then I know I have Bartonella. And can also identify which symptoms go with which based on improvement. Heck, it may be more reliable than testing! Time will tell. I am supposed to also do just Borellia only dose soon. I am not doing anything for Babesia yet so I guess if I see no improvement I will move on to it. Cost for mine was $100 but includes various titrations. My plan is to hopefully figure out what I have and then I can have a more targeted plan on killing this crap soon.

Some have titrated through all the doses and seen no improvement. According to the doctor, this means they might not even have Lyme. In these cases an autologous sample of stool, urine or whatever is taken and a custom LDI is made for you (sterilizing your stuff and mixing with enzyme). This then turns your immune system off to whatever was in your sample. Pretty interesting stuff.

I know, I get so angry but I know that won't do any good. But still, what is it going to take for people to accept this? A lot of people are saying it must not be Lyme because 3 of them have it. Ugh. People are so clueless and judgmental. She seems to be handling it all like a champ though.

It’s A Miracle! Yolanda Tells Bravo She’s Recovered From Lyme Disease Symptoms

radaronline.com/celebrity-news/yolanda-foster-lyme-disease-recovery-real-housewives-beverly-hills-reunion/

My understanding of LDI is that it can help *after* anti-infective therapies have done their job. (as in, people have killed enough bugs and remaining issues are being caused by a confused immune system)

And, yes, the ignorance surrounding Lyme (and its coinfections) mirrors that of AIDS when it was first identified.

I'm realizing how lucky I am that the few "non-forum people" I share my Lyme stories with don't openly comment to the contrary.

I'm VERY happy for Yolanda and hope she continues to spread the word. Something needs to come out of everyone's needless suffering.

It stands for Low Dose Immunotherapy. No, most LLMD's don't offer it, yet. It's still fairly new in the lyme world...but I think something similar has been used for years for allergies.

I am waiting to see how people respond before I try it.

Using LDI after antibiotic therapy would be a good approach. At that time the bacterial load should be low and hopefully your body could keep it in check. The LDI could then turn off any autoimmune reactions. Since I didn't treat with abx long, my load is probably pretty high.

I have been feeling better these past few days. However, I do still have some buzzing/numbness, noise in ear, and some new aches and pains. I am not sure if this is considered a "flare" or just my regular ups and downs that I experience. Unless you see a major symptom disappear or have a major flare, it's hard to know when you hit your core dose. This is my dilemma.

I definitely think there is value in this treatment, but I think there needs to be a plan of using it in conjunction with herbs or even abx.

I think this should link you up to a thread where I explained it.

www.healingwell.com/community/default.aspx?f=30&m=3523272