Dear Vigilius,
Yesterday I spoke with someone who was recovering from shingles and she
told me that the pain I described of my father is quite similar to what
she experienced. You see all kinds of small and slightly larger light
red spots on the skin that do not itch, but certainly no inflammation or
fluid-filled blisters. I therefore believe that maybe it is some virus
or Lyme bacterium that causes the terrible pain.
I looked up what qi stagnation is and that might be correct. Does that
give so much pain that you can hardly touch such a spot?
With kind regards,
Nikita B
Op 12-6-2011 19:44, Vigilius Haufniensis schreef:
If the pain is fixed, stabbing and worse at night, that's blood
stagnation. If it's more distending and moves around, that's qi
stagnation. Either way, it's pretty easy to treat with acupuncture or
herbs. Come see me!
Do you have a scenar?
On 6/12/2011 10:14 AM, NikitaB wrote:
Dear list members,
Thank you all very much for your kind reactions. You have given me a
few idea's and we will try to work them out consecutively.
Hereunder follow my answers to:
PTF
I learned from you what NAET is, something I have never heard of before.
For your question "is it better with more pressure?" I can inform you
that rubbing the painful spot very, very gentle is comfortable and
pressure can be raised a little bit, but cannot be raised much
because that is too painful.
May be we will go soon to a real Chinese acupuncturist if the
investigations next Thursday in the hospital have failed.
David Aubuchon
My father does not take very much CS, approx. 4 oz. at the most as he
does not like the taste of my home made CS. He has been taking
NutraMedix herbs for more than a year now and stopped only 3 weeks
ago. As father has already pain in his back for more than 2 month's
stopping with taking Samento can not correlate with his symptoms.
Next Tuesday we will go to the woman that treats him for Lyme and she
will check him out with Pronos.
Claire Shaw
Thank you for sharing your personal privacy issues. I will keep in
mind that Osteopathy was your final answer to your Lyme-related pain
issues as well as the rest. That means that that kind of therapy has
been very powerful for you.
Tony Moody
You speak about rubbing and pressing the soles of fathers feet. I
have never done so, but thank you for this hint which we will try
out. Movement exercise of the arms to engage the shoulder blades are
things he is already trying out. Further he has not been fallen or
frightened at all and I am rubbing his back daily to try to decrease
the pain.
You speak about a Calcium/magnesium supplement to relax muscles and
nerves, but my father is already getting Magnesium. As I wrote the
Calcium (daily) together with the Alendronic Acid (1x a week) has
been stopped as we suspect this to be a cause of all the pain. Look
at a forum about Alendronic Acid:
http://www.nos.org.uk/forum/Topic420-3-1.aspx
and read: "Over the last year I have experienced strange sensations
in my legs....twitching and pain. This is particularly bad at night.
I also find I suffer a lot of muscle pain on exercise as well as
lower and mid back pain." These are the same problems my father had
so he does not take these drugs any more for almost a month now. The
pain however, does not decrease yet.
Dan Nave
I am sorry, but we are not in possession of a tub for trying out
Epsom salt, but I will discuss that with the lady we will consult
next Tuesday for fighting Lyme. For the COPD father was taking
Prednisolon with an inhaler, but we have stopped that. We have tried
out a Brooks Bradley solution with DMSO+MSM+CS with the inhaler and
have continued to use that till now to keep the lungs clear from
bacteria. Supplement with CoQ10 3x 100mg is taken daily to get a
little bit of energy.
Dear people, thank you all for your kind information. I appreciate
your efforts very much.
With kind regards,
Nikita B
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