★★★★★
a loved one of mine was recently diagnosed with PSP (Progressive supranuclear palsy).
as I understood it is a very rare neurological disorder that affects body movements, walking and balance, and eye movements.
The disease is said to have a very progressive course and the typical patient lives an average of 6-9 years
in short not good.
According to the classical medicine system, there is no medication. the doctors and specialists have not prescribed anything for him either.
this I personally find a big plus.
partly because this disease is a kind of calcification of the brain (if I understood correctly) we would like to try borax.
I have already done a lot of research and found most of the infos. I have also already purchased everything; Borax, scales, measuring spoons, books, ....
I am convinced he should try Borax, he himself is still hesitant because of the following questions:
-can Borax be taken together with medication to lower cholesterol (Atorvastatin Teva 80mg, 1 per day)? what could be the effect?
-can Borax be taken together with medication to lower blood pressure (Ramipril EG 5mg, 1 per day)? what would be the effect?
the patient is my mother's partner, male, and is 62 years old, weighs 93kg and is 1m78 tall. he lives in Belgium and I live in Switzerland.
we would be very grateful if anyone here could help us or have some tips
Pieter
Lysine has no known side effects as it is considered essential amino acids. When I mean cured there were no signs of symptoms of PSP or Parkinsons Disease. Since I treated cases of this is few and all are cured I have no proof that it will work in other countries where diets are different and not enough people being treated as it is illegal to treat people. Also I give you the major remedies in practice other supplements were used but to keep things simple this is most important. Diets play important part of treatment but most earthclinic reader know that such as avoiding sweets, honey, fried foods, use of vegetable oils, ice cream, etc.
Ted
Ted's Remedies
Ted's Remedies
My father is 62 and has PSP otherwise known as Progressive Sub nuclear Palsy. The outlook is grim as he has basically been told they know nothing about the disease and there is nothing but a few clinical trials going on.
I looked into stem cell therapy but that all seemed pretty sketchy to me.
Any information that your might be able to provide would be very helpful. Thank you very kindly in advance, we sort of feel like we are on our last leg here. Very Respectfully.
Ted's Remedies
Ted's Remedies
Ted's Remedies
Ted's Remedies
I emailed you several days ago and have not heard back yet. Please excuse my impatience but my wife has just been diagnosed with PSP and it has been very devastating news.
Please, let us know a little more about you and also about your PSP cures.
Thank you.
EC: Dear Allan,
So sorry but Ted had a stroke in 2015 and is unable to correspond at this time.
Ted's Remedies
★★★★★
