Re: Lyme/question for Dudley

[Guest guest]

Dudley, Sovereign Silver is apparently the recommended brand. Is that what you

recommend if we don't want to make our own?

Thanks,

Martha

>

> Hi Zoe,

>

> If a person diagnosed with MS takes colloidal silver for two weeks and their

symptom picture changes, it is a sign that their condition somehow involves an

infective agent, which can be viral, fungal, or bacterial. It could mean that

they really have Lyme disease (or some other systemic infection) and have been

misdiagnosed. It could also mean that they have MS and a concurrent systemic

infection that has triggered or is complicating the condition. In either case, I

would keep up the CS until it is clear that it no longer has any effect.

>

> Dudley

[Guest guest]

I would recommend Utopia Silver Supplements. They are having a 1/2 off sale

right now. For more information, visit

http://tinyurl.com/2cgwxa

[Guest guest]

Thank you!

>

> I would recommend Utopia Silver Supplements. They are having a 1/2 off sale

right now. For more information, visit

>

> http://tinyurl.com/2cgwxa

>

[Guest guest]

Hi Judith,

In my opinion, exacerbations don't just happen--they happen for a

reason--usually a very good reason. That reason, I believe, in most cases, is

stress. It can come in the form of overexertion, having surgery, getting

married, getting divorced, having a death in the family, performing in public,

having an accident or injury, fighting and arguing, getting an infection, or a

number of things to which your body responds with a biochemical response

mediated by adrenaline, cortisol, and other stress hormones. Whatever its cause,

if your stress level is high enough, it will easily nullify or overrule the

beneficial effects of LDN, proper diet, colloidal minerals, food supplements,

and anything else you happen to be doing to treat your MS. In 2004, Dr.

Mohr analyzed 14 studies relating to stress and MS. He concluded stressful

events not only tend to precede the initial onset of MS, but also increase the

risk of MS exacerbations, disease progression, and lesions on MRI. Avoid stress

like the plague. The same goes for food and drink to which you are allergic,

sensitive, or intolerant.

If, despite your best efforts, you experience an exacerbation, this site

features a non-steroidal protocol that may help:

http://tinyurl.com/treating-ms-relapses

It was developed by Dr. M.R. Lawrence, an English physician who himself has MS

and who treats it with LDN.

Best regards,

Dudley

[Guest guest]

Thanks Dudley. I agree (about stress being a big factor)! In my own case, I

believe that stress is my biggest challenge. Thanks for the link. My doctor

is currently trying to get my free radicals level down, so he is giving me

some anti-oxidant supplements.

On Wed, Nov 9, 2011 at 9:54 AM, Dudley Delany wrote:

> **

>

>

> Hi Judith,

>

> In my opinion, exacerbations don't just happen--they happen for a

> reason--usually a very good reason. That reason, I believe, in most cases,

> is stress. It can come in the form of overexertion, having surgery, getting

> married, getting divorced, having a death in the family, performing in

> public, having an accident or injury, fighting and arguing, getting an

> infection, or a number of things to which your body responds with a

> biochemical response mediated by adrenaline, cortisol, and other stress

> hormones. Whatever its cause, if your stress level is high enough, it will

> easily nullify or overrule the beneficial effects of LDN, proper diet,

> colloidal minerals, food supplements, and anything else you happen to be

> doing to treat your MS. In 2004, Dr. Mohr analyzed 14 studies

> relating to stress and MS. He concluded stressful events not only tend to

> precede the initial onset of MS, but also increase the risk of MS

> exacerbations, disease progression, and lesions on MRI. Avoid stress like

> the plague. The same goes for food and drink to which you are allergic,

> sensitive, or intolerant.

>

> If, despite your best efforts, you experience an exacerbation, this site

> features a non-steroidal protocol that may help:

>

> http://tinyurl.com/treating-ms-relapses

>

> It was developed by Dr. M.R. Lawrence, an English physician who himself

> has MS and who treats it with LDN.

>

> Best regards,

>

> Dudley

>

>

>

--

" I ask God not for the grace to see what lies ahead but for the grace to

accept whatever comes. "

-- Merton

[Guest guest]

Judith

This is the time of the year that peoples vitamin d levels plunge from less

daylight hours.

What are your blood levels of vitamin d ?

Dear Dudley

I have had an awful retapse for the past 2 weeks and have not been able

to stand because I`ve had such awful spasms and heaviness iin my legs

and weakness and I could walk holding on t things . I do the BBD have

taken LDN FOR 3 YEARS take all recomended supliments and Dr Bob

Lawrence says I m doing all the right things. Do you have any ideas of

anything I can do

Judith miller

[Guest guest]

Hey;

Will step in on this question as I have been diagnosed TWICE with MS, figured

out the MS drugs were making me weaker! Figured out that I actually have

neuroborreliosis, better known as Lyme Disease.

Notes from prominent Lyme Doc Burrascano's March 21, 2011 talk;

http://sonyafightslyme.blogspot.com/2011/03/burrascano-notes-from-march-21st-tal\

k.html

Sadly, due to the length of time I was sick, about 8 years, and have taken 4

prednisone tapers AND took Rebif for one year, I am classified as a " steroid

disaster " :-( This means that I should very likely take IV antibiotics via a

PICC line or port.

My first Lyme diagnosis was done by a combination of a Fry Laboratories test,

history, symptoms, and a physical exam. The diagnosis was confirmed by my

herxheimer reaction to doxycycline.

I also have an IgeneX Lyme Disease test, which is the test many Lyme Docs like.

My second Lyme doc diagnosed me with neuroborreliosis. Currently I am taking

intramuscular antibiotics. Will be having an appointment with my LLMD #3 Nov

30. Will be discussing PICC line installation and starting IV antibiotics.

It's critical to get a good LLMD! Not all docs are a good fit. They are also

about a 3 to 6 month wait to get an appt. After about 6 months, if it's not

working, hire the next LLMD.

For symptoms www,canlyme.com

Watch the entire documentary " Under Our Skin on Hulu.

For a DVD of Burrascano's talk

http://www.lymedisease.org/lyme_store/lyme_store_burrascano.html

>

> > **

> >

> >

> > Hi Judith,

> >

> > In my opinion, exacerbations don't just happen--they happen for a

> > reason--usually a very good reason. That reason, I believe, in most cases,

> > is stress. It can come in the form of overexertion, having surgery, getting

> > married, getting divorced, having a death in the family, performing in

> > public, having an accident or injury, fighting and arguing, getting an

> > infection, or a number of things to which your body responds with a

> > biochemical response mediated by adrenaline, cortisol, and other stress

> > hormones. Whatever its cause, if your stress level is high enough, it will

> > easily nullify or overrule the beneficial effects of LDN, proper diet,

> > colloidal minerals, food supplements, and anything else you happen to be

> > doing to treat your MS. In 2004, Dr. Mohr analyzed 14 studies

> > relating to stress and MS. He concluded stressful events not only tend to

> > precede the initial onset of MS, but also increase the risk of MS

> > exacerbations, disease progression, and lesions on MRI. Avoid stress like

> > the plague. The same goes for food and drink to which you are allergic,

> > sensitive, or intolerant.

> >

> > If, despite your best efforts, you experience an exacerbation, this site

> > features a non-steroidal protocol that may help:

> >

> > http://tinyurl.com/treating-ms-relapses

> >

> > It was developed by Dr. M.R. Lawrence, an English physician who himself

> > has MS and who treats it with LDN.

> >

> > Best regards,

> >

> > Dudley

> >

> >

> >

> --

>

> " I ask God not for the grace to see what lies ahead but for the grace to

> accept whatever comes. "

>

> -- Merton

>

>

>

[Guest guest]

My blood levels of vit D are over 120 I am taking 15,000 mg day of vit

D

JUDITH

________________________________

From: mscured [mailto:mscured ] On Behalf

Of keith evans

Sent: Wednesday, November 09, 2011 4:21 PM

To: mscured

Subject: Re: Lyme/question for Dudley

Judith

This is the time of the year that peoples vitamin d levels plunge from

less

daylight hours.

What are your blood levels of vitamin d ?

On Wed, Nov 9, 2011 at 5:52 AM, J.D. <jdm@...

<mailto:jdm%40uppingham.co.uk> > wrote:

Dear Dudley

I have had an awful retapse for the past 2 weeks and have not been able

to stand because I`ve had such awful spasms and heaviness iin my legs

and weakness and I could walk holding on t things . I do the BBD have

taken LDN FOR 3 YEARS take all recomended supliments and Dr Bob

Lawrence says I m doing all the right things. Do you have any ideas of

anything I can do

Judith miller

[Guest guest]

Judith

How are you doing lately?

Have you ever been checked for infections like lyme disease or mycoplasma etc?

Sent from my iPad

> My blood levels of vit D are over 120 I am taking 15,000 mg day of vit

> D

>

> JUDITH

>

[Guest guest]

Have had TWO MS diagnoses, taken Rebif, Copaxone, LDN, and EAP. It does NOT

matter how much documentation we share w/ the physicians. Myself, used to own /

run a bio tech lab. Went to my neurologist appts wearing a tailor made shirt,

classy wool pants, wore a tie, wit my leather brief case brought in peer

reviewed journal articles I had picked up at the local medical school library.

NONE of it was any good, or even glanced at by any of my neurologists !

have also been dxd w/ Lyme disease. Dec 13, 2011 started IV Claforan. Today

started being able to stand much better.

For Symptoms

www.CanLyme.com

For diagnosis. get an IgeneX blood test. The test is a difficult read. Will

need help of Lyme Literate Medical Doctor (LLMD)

Some videos

Lyme Disease - MS Misdiagnosis

http://vimeo.com/2354218

Lyme Disease documentary (trailer)

http://www.youtube.com/watch?v=uSsnMQHIJZk

Canadian television " Out of the Wild "

http://www.ctv.ca/CTVNews/WFive/20091113/w5_lyme_091114/

I sleep a lot. Feel free to send a note to wake me up :-)

>

> Hi my name is and I was diagnosed with MS in 2002 in Florida.  I moved

to Mass and live on disability.  I was taking Copaxone and it was helping.  When

I moved here, I stupidly signed up for a health program run by the state.  One

of the reasons I signed up for it was because all my prescriptions were free. 

But I don't get the choice of physician.  Their physician says he doesn't think

I have MS and discontinued my Copaxone. He is a GP.  Since then I have continued

to go downhill,especially my thought processes.  I brought 40 pages of medical

records with me from the neurologist in Florida, but this quack say I have

peripheral neuropathy.  That way they don't have to pay $1800 a month for my

Copaxone.  And so I'm stuck.  Because of living on disability, I can't afford to

get off the program and pay 20% of the healthcare and co-payments on the

prescriptions.  Has anybody else had this problem?