The internet is a safe haven for people to act nasty, but it is also representative of cultural opinion at large. Based on this knowledge, I am extraordinarily dismayed that with all the PSA’s for Lyme Disease and new info circulating around it, it still doesn’t “count” as a serious illness to many people.
Of course all the details about my late stage neurological Lyme, like how I had fibromyalgia so bad I couldn’t move my limbs for a spell, were cut from Chopped, and the CO poisoning was played up because it made me look insane that a stove tried to kill me. The reactions from people, though, were still shocking: I didn’t have cancer, how could I call myself a survivor? My illnesses didn’t compare to cancer. The other two contestants had cancer, and I need to GET OVER MYSELF. Never mind that my CO poisoning– which I have very real blood work and medical records from, just like my Lyme– involved a diagnosis of Alzheimer’s by a Cedars Sinai neurologist, and the gas killed my ex’s cat, it was considered “trite” compared to cancer.
Lyme disease has a tendency to keep people laid up for years, and many simply never get well. There is no “cure,” only methods of treatment that very thankfully work for some, like me. My family and I did intensive research to find holistic treatments for both my illnesses when they each occurred, and thankfully, I successfully moved past both. My mom had cancer, and was mortified when I told her yesterday about people’s statements of my illnesses being “nothing” compared. Pain and suffering are pain and suffering, and one thing that can kill you is no less bad than another thing that can kill you.
There is simply no need, ever, to compare illnesses and minimize the suffering of others. People used the hashtag “#killerstoves” to mock my experience as minimal compared to cancer. Some even said there is no way it happened, because I’d be dead, which is clearly untrue: the ventilation problem was real, and was fixed by real HVAC people. The exposure was slow and low and not detectable on an alarm designed to only detect life threatening levels. It left me with a huge array of brain damage related troubles, all of which I have recovered from fully via holistic methods. (And most definitely NOT only with avocados, that was some fun editing.)
Our culture is rife with judgment, and social media fuels our ability to depersonalize others. We are all critics from our couches. I write this not to say I feel I was perceived unfairly (that’s a whole different blog!), but to ask people to realize that being laid up for years is a nightmare, whether or not one is sick with cancer. Period.
Besides, you know, affecting people’s lives positively and stuff, my recent speech for the Lyme Angeles Lyme disease group has gotten me to finally remember how to spell the word e-x-c-e-r-p-t. It’s one of my only spelling nemeses, and I’ve had to use it repeatedly when posting clips (aka excerpts) from my speech. Now I’m confident that I can spell it in my sleep. I’m equally confident that you will learn something from at least one of these three video clips from my speech! =)
Just because you can put it in your body, doesn’t mean you should
Let’s talk sugar, sugar
I hope you have hope
PLEASE NOTE: Due to the volume of inquiries I receive requesting help for Lyme Disease, I am unable to reply to all blog comments and emails. If you are interested in scheduling a phone or Skype consultation with me on treating Lyme Disease naturally, please contact me directly by email or phone.
So far, I’ve had Lyme Disease and Bartonella in complete remission for 4 years, and that includes having spent 6-8 months minimum getting seriously exposed to carbon monoxide. If one can get hardcore chronic CO poisoning and still not relapse, I think it’s safe to say their treatment system was damn successful. In total, I dealt with Lyme for about 2 1/2 years before getting it into remission, which is shorter than many people out there, but still long enough for it to have taken over my body on a cellular level. At my worst, I had fibromyalgia so bad that my legs would not bend enough for me to walk.
I have a document that I’ve sent to many people with everything I did to get well, and decided it was time to post it here for the interwebs at large to have access to. Some things are more personal than I’d really care to share publicly, but I am doing so for the sake of hoping to help others. Note that this is just what worked for ME, and is not medical advice from a professional. I’m just a health foodie chef girl who manages to survive an array of wacky illnesses and wants to share whatever possible to help others recover too.
Lyme Success- What I Did:
-The #1 thing that killed the Lyme was a GB 4000 rife machine. It costs about $2500, my parents bought it for me. Basically, it is a
radio frequency machine that bursts both the lyme and the cysts the disease creates inside your cells to protect itself from being killed.
(Antibiotics make the lyme build stronger and stronger cyst protections, which is why people plateau so quickly on them.) I also
found useful the rife’s programs/settings for pain, detox, etc. A cheaper option is a doug coil, which can be homemade, or a Hulda Clark Zapper. Though the cost of the GB 4000 is high, it is cheaper than antibiotics and all their supplies, and much more effective.
-Therapy helped a lot with the entire process. Lyme eats up your brain and creates whacked out, f-ed up emotional problems; I would sit in the closet in the dark and cry for hours, with no cause or understanding of why. I’d always been pretty stable before, that
wasn’t normal for me at all and was very scary. I also had a LOT of awful suicidal thoughts that came as soon as any conflict arose in
life. I just couldn’t deal with anything without feeling overwhelmed and like I wanted to die. Therapy not only got rid of all that, it
gave me hope that I would get better, which in turn, I did. I did DNMS, developmental needs meeting strategy, along with EMDR, eye movement desensitization reprocessing. My therapist taught me how to be sick, and then, how to be a better version of myself when I got well.
-Supplements are VITAL. I took daily all of the following: sarsaparilla root, pau d’arco, chlorella, milk thistle, probiotics, proteolytic enzymes, zeolite, krill oil, olive leaf, magnesium, immunity mushroom blend, ubiquinol, and a multiple with high amounts of b/c/d etc. plus an antioxidant blend.
-Acupuncture was the thing that actually catapulted me into wellness. I had already killed the lyme, but was so overrun with toxins I couldn’t get out that I hadn’t yet felt any recovery. Acupuncture, specifically the mobile cupping, mobilized the toxins out, and I began recovering the day in late December 2010 that I first had it done.
-Coffee enemas. I know, major wtf. But seriously, they helped a lot. There is pretty much NO way you can get out all the toxins building up from killing lyme without drastic actions. Google has all the info on how the caffeine stimulates your liver to dump the toxins out. I did these twice a week, minimum.
-Epsom salt baths with hydrogen peroxide, after every rife treatment. They help pull the toxins out through your skin.
-Diet. I’ve always been an extreme health foodie, but I had to go as far as cutting out all grains, fruit, etc. for awhile. Lyme makes bad
stuff grow in your intestines, and both ibs and candida are very common in Lyme patients, so you can’t feed the yeast or it makes the
Lyme stronger by creating a more acidic internal environment. Incidentally, I had horrific ibs before being diagnosed and fixed both
that and the major candida symptoms with a product called Intestinew by Renew Life. Organic, unprocessed food is key.
-Kombucha. I drank 16-32 oz a day, which is pricey, but it’s the only thing that ever helped me palpably feel better, plus it’s full of
-E3 Live: again, pricey. It’s a good way to get high potency greens, but I didn’t feel it really helped until I was already on the way to
-For insomnia, they gave me ketamine, to which I said no way. I managed to sleep with large doses of amantilla, which is valerian root
extract, and a chinese herbal complex called an shui wan.
-For pain, a topical cream called Thermoderm provided substantial relief. It’s cheap. Also, pot helped with pain, specifically pot with
a low thc to high cannabanoid ratio.
As for what to avoid:
-Lyme disease forums on which everyone is still ill. Majorly depressing.
-Antibiotics if possible, which only have a 65% recovery rate and a 35% relapse rate anyway and will likely ruin one’s digestive system indefinitely. They are the standard course of treatment.
-Cowden Protocol, or herbs from it. The herx (die off reaction) is the worst ever… like bugs crawling all over you, bad drug trip, tear
your eyes out, bad. This includes samento, cumanda, and the other herbal antimicrobials. The herbs with it like burbur, pinella,
magnesium malate, and serrapeptase are fine.
The Number One Lesson That Helped Me:
In my interview with the fabulous Blythe of Blythe Raw Live, I detailed my process with Lyme, as well as the statement from my therapist that was utterly transformational to my healing process. The Lyme clip is only about five minutes total and has some good info, but if you don’t want to watch it all, fast forward to about four minutes in for that part. I think it’s the most powerful when spoken. You can watch it here.
Again, I’m no professional! I grew up in a very holistic household that taught me to always choose natural remedies before Western Medicine when possible. In my opinion and experience, that is the smartest, most productive, and best way to go for overall health.