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Just spotted this : http://www.bbc.com/future/story/20150327-how-a-bee-sting-saved-my-life
Now where is the closest hive?
Now where is the closest hive?
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How a Bee Sting Saved My Life
Ellie Lobel - Mosaic - 3/24/2015
Ellie Lobel was ready to die. Then she was attacked by bees. Christie Wilcox hears how venom can be a saviour.
"I moved to California to die."
Ellie Lobel was 27 when she was bitten by a tick and contracted Lyme disease. And she was not yet 45 when she decided to give up fighting for survival.
Caused by corkscrew-shaped bacteria called Borrelia burgdorferi, which enter the body through the bite of a tick, Lyme disease is diagnosed in around 300,000 people every year in the United States. It kills almost none of these people, and is by and large curable – if caught in time. If doctors correctly identify the cause of the illness early on, antibiotics can wipe out the bacteria quickly before they spread through the heart, joints and nervous system.
But back in the spring of 1996, Ellie didn't know to look for the characteristic bull's-eye rash when she was bitten – she thought it was just a weird spider bite. Then came three months with flu-like symptoms and horrible pains that moved around the body. Ellie was a fit, active woman with three kids, but her body did not know how to handle this new invader. She was incapacitated. "It was all I could do to get my head up off the pillow," Ellie remembers.
Her first doctor told her it was just a virus, and it would run its course. So did the next. As time wore on, Ellie went to doctor after doctor, each giving her a different diagnosis. Multiple sclerosis. Lupus. Rheumatoid arthritis. Fibromyalgia. None of them realised she was infected with Borrelia until more than a year after she contracted the disease – and by then, it was far too late. Lyme bacteria are exceptionally good at adapting, with some evidence that they may be capable of dodging both the immune system and the arsenal of antibiotics currently available. Borrelia are able to live all over the body, including the brain, leading to neurological symptoms. And even with antibiotic treatment, 10–20 per cent of patients don't get better right away. There are testimonies of symptoms persisting – sometimes even resurfacing decades after the initial infection – though the exact cause of such post-treatment Lyme disease syndrome is a topic of debate among Lyme scientists.
"I just kept doing this treatment and that treatment," says Ellie. Her condition was constantly worsening. She describes being stuck in bed or a wheelchair, not being able to think clearly, feeling like she'd lost her short-term memory and not feeling "smart" anymore. Ellie kept fighting, with every antibiotic, every pharmaceutical, every holistic treatment she could find. "With some things I would get better for a little while, and then I would just relapse right back into this horrible Lyme nightmare. And with every relapse it got worse."
After fifteen years, she gave up.
(...)
http://gizmodo.com/how-a-bee-sting-saved-my-life-1693295289
"I had been living in this… I call it a brown-out because it's like you're walking around in a half-coma all the time with the inflammation of your brain from the Lyme. My brain just came right out of that fog. I thought: I can actually think clearly for the first time in years."
I received injections of bee venom in 2006 before I was aware of my TBD's. There's a guy in Toronto named, Ravikovic, who administers them for Asthma, allergies, and sensitivities. I got a boost from them that would last until the end of the day, but no lasting improvement.