I completed my gut
healing protocol last month and that meant adding dairy, nightshades and grains
back into my diet. As with any foods that are removed from your diet for a
prolonged length of time you should add the food back into your diet gradually
in 3 day increments and always paying attention to any symptoms or flare-ups…
so I added dairy, then grains, then nightshades [tomato, potato (not sweet
potato), eggplant, peppers (not black pepper)]. The same day I added
nightshades I had one of the worst Chostochondritis flare-ups I have ever
experienced, fortunately it was also one of the shortest flare-ups I’ve ever
had. I’m sure you realize what all of this means… I have to remove nightshades
from my diet, a tough thing to do if you are one of those individuals that
enjoys foods from a multitude of cultures. That said, nightshades were not
something I ate frequently, but makes it difficult to eat out. The choices are
limited, but not impossible.
Nightshade 101 - There
are many wives tales about the reason nightshades got their name, but the truth
is that these plants are in growth mode during the shade of the night. These
plants actually have toxic qualities, certain alkaloids, if eaten in large
quantities can be toxic especially in individuals that are sensitive. One
nightshade plant that is easy to identify by most as toxic is the nicotine
plant. Always be sure to cook your nightshade plants as this will cut the
alkaloids by 50% and make sure to store potatoes in a dark dry place and not in
the sun as the sun will increase the alkaloids in potatoes and make sure not to
eat any nightshade plant if it is green unless it is supposed to be green (ie.
heirloom tomatoes or green bell peppers, jalapenos...). Also, do not forget to
cut all eyes and sprouts out of potatoes before preparing them to eat.
Nightshade plants are a problem for 1 in 3 people with arthritis and perhaps
with any "itis" type of condition. Costochondritis is considered a
form of arthritis.
In addition I had
several Herxheimer (herx) reactions to the Cat’s Claw. Some were minor skin
reactions that lasted less than 24 hours and then I hit the mother load of
herx. I had large patches of what I think were hives that felt like razor burn
on my inner thighs. This lasted about a week before it started to calm down and
made the Epsom salts baths difficult without adding baking soda. This reaction
was followed by a herx of head to toe musculoskeletal pain and got so bad that
it felt like rigor mortis was setting in. This reaction also lasted about
another 7-10 days and I still have lingering fatigue from that episode that
seems to wax and wane. I’m not at a full dose of Cat’s Claw yet. The ultimate
goal is 45 drops 3xs/day. I’m at 35 drops 3xs/day. With each herx I have to
stay at the dose I’m at when the herx happens and then increase once symptoms
begin to subside. I feel fortunate because herx reactions can last up to 3
weeks and I’m so glad that it did not last that long. It took every effort I
had in my body to make it to work during this time and to make it through the
day. I even kept up with my workouts, which in retrospect I should have slept
in. That was what my body really needed, but I didn’t realize what was
happening until half way in. I’ll definitely know to stay in bed if there is a
next time, but I’m hoping there is not a next time.
Nightshade )-: |
For now, I’m waiting on
some lab work to come back. We’re looking for parasites an Candida overgrowth
once again… lucky me. These are things I am much more susceptible to with
chronic Lyme in the picture.
We are also taking a
look at food intolerances measured by an IgG immune response. As much as
adjusting to new dietary restrictions sucks, I’m pretty used to it at this
point and willing to remove foods from my diet for a length of time to give my
immune system a break so that it can focus on healing Lyme and co-infections.
I’ve come across some
helpful websites and research along this new adventure in my health. One in
particular offers an opportunity to participate in webinars and you can submit
your own questions about chronic Lyme while the doctor (Marty Ross, MD) answers
questions live via webcam on given dates/times. I haven’t participated yet, but
plan to do so. The webinars are recorded, so you can replay them any time after
they are recorded. Take a look at the blog and webinar recordings if you have
an interest: Lyme Webinar/blog
I also found that
Dietrich Klinghardt PhD/MD seems to have wonderful alternative protocol
suggestions for chronic Lyme and its co-infection and multitude of other issues
it brings. I don’t know if my protocol will be similar, but his is one that
makes sense to me. Take a look: Lyme protocol
I also want to say
something to all my Hashimoto’s readers. Hashimoto’s can often be an underlying
symptom of chronic Lyme. I’m not suggesting that everyone with Hashimoto’s has
Lyme disease, but if you are struggling with treatment, it may be something to
consider. In my case I believe
that the Lyme disease was actually one of the causes of my Hashimoto’s and
other autoimmune disease and that is the case for many folks with chronic Lyme
and autoimmune conditions. Often the Lyme shows up first, but is diagnosed
last. Here is a quote from Dr. Klinghardt, “Chronic Lyme disease is a
fast-spreading problem in the USA and worldwide. Classical Lyme disease is
caused by a bacterial spirochete called Borrelia burgdorferi. Conventional belief attributes Lyme Disease
conveyance through tick bites. Interestingly to the physician, more recent
literature has shown that also certain stinging flies, spiders and even some
mosquitoes can infect humans with this spirochete. This means that the disease
vector can be more widespread than previously anticipated.”
by Dr. Nikolas R. Hedberg of The Lyme-Thyroid Connection says this, “Lyme disease can have devastating effects on the body and can trigger autoimmune diseases such as Hashimoto's Thyroiditis. The bacteria borrelia burgdorferi has been found to cross-react with thyroid tissue which triggers the autoimmunity by what is known as molecular mimicry. This basically means that your immune system tags an infectious agent but also attacks self-tissue that has a similar protein structure.”
None of this information intended to cause alarm. I want to encourage patients to become educated about any chronic disease(s) you may have. Autoimmune diseases are complicated and doctors do not know everything. No one knows what it feels like to live in your body, so as the patient you need to be in the driver seat and learn all that you can about your chronic disease(s). The good doctors will admit that they don't know everything. The good doctors are constantly learning from new research and new findings and are not complacent in their practice. I am constantly reminded how thankful I am for the wonderful practitioners who support and encourage me and who work hard on my behalf and who pick me up when things get difficult and who are non-complacent in their practice. Thank you, just never seems to really say how grateful I am.
Wow, this is another post full of new info for me. Thanks for sharing your knowledge about Lyme's. I definitely thought that the origin was from a tick bite.
ReplyDeleteWhat a bummer about the food restrictions! Please let us know about your IgG test experience. I am very interested in learning more about this.
My hubby has serotonin issues and had major gut issues as well. Once we learned that most of the serotonin in the body is produced by the gut rather than the brain, he started working to heal his. As I'm sure you can relate, it has been a long road for him but he is making progress. His serotonin issues seem to be greatly improving (as well a his daily physical comfort - hooray!).
Anyway, hope the test results came back just as you hoped for. Sending healing thoughts your way :)
Yes, a bummer about the food restrictions, but anymore these days it has been pretty common and something I'm used to. I'll find out about the IgG results lat next week. Should be intersting to find out the results.
ReplyDeleteI'm glad your hubby is experiencing improvement. That is encouraging.
Thanks for the post. I'll provide an update next month.