Re: Dr. Bihari's Parkinson's patients???

[Guest guest]

Hi ,

My father has been taking LDN for PD since October

2004 and is doing very well. He started out at 3mg

and now takes 5mg. We have seen no progression and he

has had remission in all of his muscle tension

throughout his body. We started LDN because his

breathing was beginning to shudder from muscle

tightness. He has had PD for 14 years. He underwent

DBS May 2004 and suffered a massive hemorrhaghic

stroke that left him paralyzed on his left side.

Today he continues to recuperate from the stroke and

PD. We are documenting everything from medications to

each new sustainable success. His medication needs

went down from 10 25/100 Sinemet to 5 Sinemet. He use

to take 3 .25 PErmax and no longer does.

He still continued to have problems with fatigue and

tremor so we have continued to try new therapies in

addition to LDN. WE are currently in Chico, CA and he

is doing hyperbaric oxygen therapy and glutathion

treatments. Today is day four and each day we are

seeing results. HIs medication effectiveness and

amounts are 2 to 3 Sinemet on the day of and day after

using glutathion. HIs energy level, speech and

swallow are also better.

I believe that LDN is a very important piece of the

puzzle and is essential to his continued success. I

also believe it is worth considering glutathion and

hyperbaric oxygen therapy. I will keep posting info

on his success over this next month.

Good Luck. Please feel free to contact me if you have

any further questions at destinyellen@....

Sincerely,

Destiny

--- maxwell98king <wjkeeman@...> wrote:

> Hello, in the LDN website and in his keynote address

> to the 1st LDN

> Conference, it is mentioned that Dr. Bihari has

> treated with LDN about

> ten patients who have Parkinson's, some for about

> four years. Dr. B

> claims all have shown no progression in their

> disease. Do any of these

> patients belong to this chat group? I have never

> seen them here, why

> not? It would be VERY Encouraging if these people

> could relate their

> experience with LDN to others who have PD. Could Dr.

> Bihari encourage

> them to join this group? I belive there are not many

> of us PD'ers

> taking LDN for this disease and we are not getting

> much feedback on if

> the stuff works as claimed.

> Sincerely,

>

>

>

______________________________________________________

for Good

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[Guest guest]

Hi Destiny,

Do you have a summary of your father's health success story, and if so, would you be happy to share it through the 'Case Health - Health Success Stories' website?

Regards,

Cris

Re: [low dose naltrexone] Dr. Bihari's Parkinson's patients???

Hi ,My father has been taking LDN for PD since October2004 and is doing very well. He started out at 3mgand now takes 5mg. We have seen no progression and hehas had remission in all of his muscle tensionthroughout his body. We started LDN because hisbreathing was beginning to shudder from muscletightness. He has had PD for 14 years. He underwentDBS May 2004 and suffered a massive hemorrhaghicstroke that left him paralyzed on his left side. Today he continues to recuperate from the stroke andPD. We are documenting everything from medications toeach new sustainable success. His medication needswent down from 10 25/100 Sinemet to 5 Sinemet. He useto take 3 .25 PErmax and no longer does. He still continued to have problems with fatigue andtremor so we have continued to try new therapies inaddition to LDN. WE are currently in Chico, CA and heis doing hyperbaric oxygen therapy and glutathiontreatments. Today is day four and each day we areseeing results. HIs medication effectiveness andamounts are 2 to 3 Sinemet on the day of and day afterusing glutathion. HIs energy level, speech andswallow are also better. I believe that LDN is a very important piece of thepuzzle and is essential to his continued success. Ialso believe it is worth considering glutathion andhyperbaric oxygen therapy. I will keep posting infoon his success over this next month.Good Luck. Please feel free to contact me if you haveany further questions at destinyellen@....Sincerely,Destiny--- maxwell98king <wjkeeman@...> wrote:> Hello, in the LDN website and in his keynote address> to the 1st LDN> Conference, it is mentioned that Dr. Bihari has> treated with LDN about> ten patients who have Parkinson's, some for about> four years. Dr. B> claims all have shown no progression in their> disease. Do any of these> patients belong to this chat group? I have never> seen them here, why> not? It would be VERY Encouraging if these people> could relate their> experience with LDN to others who have PD. Could Dr.> Bihari encourage> them to join this group? I belive there are not many> of us PD'ers> taking LDN for this disease and we are not getting> much feedback on if> the stuff works as claimed. > Sincerely, > > > ______________________________________________________ for Good Donate to the Hurricane Katrina relief effort. http://store./redcross-donate3/

[Guest guest]

Hi .. My uncle with PD is on 4.5mg LDN since sept 2002. He

developed PD about 3 years prior. He has never taken any PD meds

mainly because he cannot tolerate meds. He has a sensitive stomach.

LDN he can tolerate. I will report honestly. My uncle has not

experienced anything brand new so always remember that is the bottom

line. However, I do think that the tremor he had originally in his arm

and leg is now worse. I will not panic until he develops a brand new

symptom because the guy works 14 hour days in shipyards .. and he is

over 60. I believe that LDN is helping him without question .. it is

definitely slowing progression. Is it stopping PD progression like I

believe it stops MS .. only time will tell because PD progresses

slower than MS .. I think we have to wait longer for a more definite

answer.

All the Best

Shameless Plug .. www.marybradleybooks.com

> Hello, in the LDN website and in his keynote address to the 1st LDN

> Conference, it is mentioned that Dr. Bihari has treated with LDN

about

> ten patients who have Parkinson's, some for about four years. Dr. B

> claims all have shown no progression in their disease. Do any of

these

> patients belong to this chat group? I have never seen them here, why

> not? It would be VERY Encouraging if these people could relate their

> experience with LDN to others who have PD. Could Dr. Bihari encourage

> them to join this group? I belive there are not many of us PD'ers

> taking LDN for this disease and we are not getting much feedback on

if

> the stuff works as claimed.

> Sincerely,