MoFoYoFo does have a screw loose, she is MORE dangerous than Brooks Ayers - Brooks was scamming one woman, Yoyo is scamming a whole group of people.
Forgive me if I am going over old territory but collectively? All her BS is just that, A pile of BS.
Her leaking implants are suspect. Leaking silicone, into the body, does impact your lymphatic system and your body wants to reject anything that irritates or doesn't 'belong' in the body.
Think of it like a splinter? Your body surrounds a foreign body with lymph (pus) and slowly tries to work it out of the area. Something like a mass of silicone would really jack your lymphatic system up - you'd have problems.
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Someone before had mentioned that there hasn't been one doctor to champion her diagnosis.
Knowing physicians/doctors/providers and the way they work? IF there was a doctor or group working with her, they would be MORE than happy to make statements or speak on her behalf in order to get the public up to speed about the disease and possibly getting more support for research? Money for the study of any disease is and can be a HUGE business.
The only 'word' we have about her illness is a binder, a closet full of pills, potions and poultices, and a posterboard with colored Post-Its with the "Illness du-jour".
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Aside from a dentist visit and her surgery? We haven't really seen any interaction with a 'doctor' for her LD/Exaggeration Disease (ED). We see every needle stick, IV, pill bottle, bariatric treatment (bariatric treatment, WTF?) and monkey scrotum injection, but don't see anything of worth from anyone who is qualified to comment on the disease?
IF she was really serious - I don't doubt her sincerity, it's her honesty that bugs me - about getting treatment for LD/ED, she'd find the best doctor and stick with their treatment regime.
MoFoYoFo IS a doctor shopper - When she doesn't get the answer she wants - she goes to find a doc that WILL entertain HER ideas of what she has. I tend to think that most docs wouldn't lead you on to make money, but when you offer 'groundbreaking treatments' that aren't offered or OK'ed by the FDA/USA/AMA that would put scads of dollars into your pockets?
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Another thing to consider are the privacy laws /HIPPA laws that prohibit any provider to make your medical files/records public, unless they have your permission. So, in essence, no one can come out and say anything about your medical history. We can go back to Brook Ayers Incident and see that HIS downfall was mentioning a medical center and making up a bunk scan/x-ray?
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One other problem with her and the kids having LD was from someone who did more research and checked the LA County Health Department website.
I can't remember the exact numbers but in more than 3 million people living in Los Angeles, there were only a handful - less than 5 -
that had the disease and 4 of them contracted it outside of LA. IF she and her kids were diagnosed in the area, that would have made the news - I lived in LA and the LACOHD was rabid about putting out the word outbreaks of anything - Hanta Virus, West Nile Virus, Rabies and all kinds of other creepy crawlies that might break out?
Had they all picked up LD from horses and the ticks in the area? The horse stables would have been quarantined and you can be sure it would have made the news. (And why would you want your daughter to go back to train with horses to pursue an bid for the Olympics if there was a chance she'd be 'reinfected'?)
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Lyme's IS one of those afflictions a doctor just cannot look at you and diagnose - and there are some other illnesses that share the same ?symptomology - which is why they are hard to pinpoint. I won't say she WASN'T ill with something, It's just what that illness is/was. I am skeptical?