Lou Gehrig's Disease > Ted's Remedies for Lou Gehrig's Disease > Ted's Remedies
Ted's RemediesQuestion by T. (Usa) on 12/27/2014
Hope you are doing very well. I have been reading your information given on ALS at Earthclinic and appreciate your time, effort, and knowledge given in the subject of remedying ALS.
I would like to ask you, when your time allows, the protocol you would suggest for my dad as he has been diagnosed with
ALS.
The primary problem now, and what seems to be in his case, the initial symptoms he had experienced, is breathing problems. A little more than a year ago he was finding himself short of breath on a walk, then this past March he noticed when he went to lay down flat, he could not breath comfortably, in July he started mentioning it a little more, we went for another walk, and I found his endurance had severely diminished.
We initially thought it may be blood vessel blockage, but when seen by a cardiologist, the cardiologist noticed twitching in his upper body and referred him to a neurologist. We didn't get very far with the neurologist, my dad had gotten himself out of breath one day, we brought him to the hospital, they put him on oxygen, he was fine for a while, then his CO2 level went very high. That seems to be the greatest problem right now. They are saying due to ALS, his neuromuscular action in his chest is not sufficient enough to engage his lungs as proficiently as they should be. He can take a good inhale but does not exhale proficiently. We can see in the lower third of his lungs in an xray there is white which is said to be from hypo-trophy of the lungs due to ALS. His arm and leg strength has never been terrible, they are only now showing deterioration due to the ALS but more so the amount of time in bed.
So right now he is on a trach with a vent. He went on the vent 28 Oct 2014. He has a lot of anxiety which is not helping his coping with the trach and vent. He is also on a peg tube for feeding.
May I ask you when you are able, would you please lay out what your protocol would be with him if he were to come to your office at this point.
In the reading at earthclinic, I see there may be an initial 48 hour regimen you may use, then a maintenance regimen after that. If you could address the ALS, and also anything that would help support his lungs while we stop the ALS.
If you could prescribe it as something like:
"For the first 48 hours for ALS I would prescribe: item "A", the dosage, and the time of day to take each dosage item "B", dosage, time of day, etc.... for ALS maintenance I would do/take this: For lung support I would initially do/take "this" at this dosage, for "this" amount of time, and maintenance would then be "this"
Also anything for anxiety you would suggest
If you would include any topical treatment as well as the internal elements you would list above, I would forever be grateful.
Thank you very much for your time Mr. Ted, my appreciation could never be justified with words. Take good care, thank you again, and I'll look forward to hearing from you when able.
Replied by Ted (Bangkok, Thailand) on 12/27/2014
Replied by Hhk (Austin, Texas) on 04/27/2015
Have been on your treatment for about a year...
Just found you posting again and was reading about polylysine and having hard time finding any where to buy it... do you know of any sources
How else have you updated your protocol
Thanks
Replied by Sara (Wisconsin) on 06/06/2015
Thank you, Sara
Replied by William (Texas) on 02/09/2017
Replied by William (Texas) on 07/08/2017
Replied by Oyinlola (London) on 03/08/2024
Please see the below.
Had progressive muscle issues since September last year. I started twitching less than some months after. The weakness is now on both arms and tongue. I started using Tudca hoping this can help and was wondering if you have an updated plan on nerve issues
Back to Ted's Remedies for Lou Gehrig's Disease