From: | Andrew |
Sent on: | Sunday, August 14, 2016, 2:43 PM |
Andrew, can you explain the procedure for sprouting grains?
And nuts? Do you mean you put walnuts in water? wouldn't they
be awful, soft and sort of rotten? Would be so helpful if you could
actually explain the procedures. People talk about sprouting a lot
but never explain it. Thanks so much in advance.
Jodie
--------------------------------------------
On Sun, 8/14/16, Andrew <East-Bay-L-E-A-P-S-list@meetup.com > wrote:
Subject: Re: [East-Bay-L-E-A-P-S] Getting frustrated, anyone have ideas?
To: East-Bay-L-E-A-P-S-list@meetup.com
Date: Sunday, August 14, 2016, 2:22 PM
http://www.meetup.com/East-
Most likely
your gut/immune system is compromised. This is why the
problems are here in the first place -and one of the reasons
the gut is compromised is because we've eaten grains
without soaking or sprouting them our whole lives, so they
tumble around like rocks in our stomach unfortunately. For
awhile, if you eat bone broth, meat, chicken, sauerkraut,
green veggies, and stay away from grains - you should see a
gradual reduction in symptoms over time. Also, nuts and
seeds need to be sprouted or soaked. Otherwise they beat up
the stomach too. Diet is a huge part; wish I'd known it
earlier. Good luck!
On Sat, Aug 13, 2016
at 8:27 PM, Angela Arthur <East-Bay-L-E-A-P-S-list@meetup.com >
wrote:
Dear Christine,
You need to find the right doctor. Find a doctor
who treats "empirically". That's the code word
for a doctor who will treat based in symptoms and
doesn't need to see a positive Lyme test. The other
thing to ask or find out is whether or not that doctor sees
Lyme as a " clinical" diagnosis.
I'm not up on who is pracitcing in the Bay
Area right now, but others on this list can probably point
you in their direction.
Don't discount naturopaths and nurse
practitioners. They are some extremely good ones who are
doing good work w Lyme.
The two practitoners I know of off the top of my
head that might be worth looking into are Mischa Greider in
SF (I don't know if he needs a + lyme test or not), and
Jake Wardwell, who practices at a couple different places in
the city.
Forget about it being covered by
insurance. Depending on your plan, You might be able to get
partial reimbursement.
I'm so sorry and keep us
posted-!
PS: there are 2 other things that
might coukd be causing your
symptoms:
--heavy metals from dental work.
Do you have a lot of dental work? Sometimes the combo of
metals and positioning in a persons head can even cause a
"battery" effect where they're basically being
zapped.
--Mold exposure + some other
compounding factor (Lyme, dental,
etc).
Don't give up!! And if
you're feeling disxouraged, go watch Under Our Skin.
You're not alone....
On Saturday, August 13, 2016, Joe <East-Bay-L-E-A-P-S-list@
meetup.com> wrote:
Hi Christine,
We all on this list sympathize intensely with
you. You are not alone.
I believe I have lyme & babesia, though like
you, I have tested negative for nearly everything (lyme
western blot, spinal tap, mri, emg, etc.). I tested low for
Vit D3, (which Im told most adults over 35 are low) &
thats about it. One test that I highly recommend is the
CD-57. Ive heard different ranges, my doc says anything
below 250 signifies lyme disease, mine was 48. Mainstream
medicine says anything below 60 is significant but really
they ignore the CD-57. Basically CD-57 is a small piece of
our immune system. If its low, it signifies that portion of
our immune system is tired out from fighting an unknown
infection. If you test positive, at least you know you are
fighting an infection & have been for
sometime.
Regarding your diet, very good, my recommendation
is to cut out the potatoes & rice. :(
Good luck & God Bless, stay tuned with us
& keep us posted.
On Aug 13, 2016, at
1:02 PM, Christine <East-Bay-L-E-A-P-S-list@meetu p.com>
wrote:
Hello
Everyone,
Sorry for the long email, I'm really
struggling right now and looking to see if anyone has had
similar experiences and if you were able to find a solution.
I've been trying to get a diagnosis for 4
years now and have come up negative on EVERYTHING. I've
been told by several doctors that they suspect I have Lyme
or MS but all tests come back perfect. I've had tons of
blood work, multiple MRI, spinal tap and EMG. I've kept
my symptoms in check with a healthy diet, light exercise and
herbal medicine, but lately I've been getting worse and
my doctors have told me there is nothing they can do. They
just give me prescription strength Ibuprofen and tell me to
keep working as long as possible and do more physical
therapy (I can probably teach physical therapy myself at
this point).
All the symptoms are on my right side; pain,
weakness, tight muscles, my foot gets cold and blue, brain
zaps, touching becomes painful, fatigue, etc. I'm sure
you get the picture. In addition I have extremely quick
reflexes according to my doctors. Exercise is difficult for
me as it triggers pain attacks 90% of the time so I have to
be VERY careful with what I do. I use to dance, hike camp
and go horseback riding so this has been the most difficult
thing for me to adjust to. I'm also in the 2% of the
population that has a 'paradoxical' reaction to
medications meaning I can't tolerate a majority of
medicines which makes it hard to treat me with western
medicine.
I don't remember ever being bit by a tick or
seeing any sign of being bit by a tick. I have been bit by
lots of mosquitoes as they seem to think I am delicious. I
swell up very badly from mosquito bites so I know when one
has bit me.
I do 15-30 min physical therapy a day as
tolerated, take a daily hour walk as tolerated, meditate,
qui gong, and I'm still working (an accomplishment in
itself). I even went vegan for several months but it
didn't seem to make a difference for me so I went back
to eating small amounts of meat (<4 oz per day). I
basically eat paleo + rice and potatoes. I get worse if I
eat sugar, gluten or processed foods so I avoid them like
the plague. I take ibuprofen, voltaren gel, effexor and
amitriptyline for pain and muscle tension. I use essential
oils and herbs to help me sleep, reduce pain and reduce
stress.
Has anyone had an experience like this? Did you
ever get a diagnosis? What, if anything, helped you? I'm
also looking for recommendations for doctors that may be
helpful or tests that I should look into. I've tried
everything I can think of and am out of options at this
point. Any advice is appreciated.
Thank you, Christine
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