Update and more

[Guest guest]

Hi Everyone,

I planned to comment on the conference and update my progress on LDN,

then shortly after the conference I was hospitalized with a pulmonary

embolism for 11 days and have not been able to shake off the creepy

depression that followed me home from the hospital. I hope my post

makes sense and gives encouragement to any who have not yet seen

expected results. Please remember though it varies from one

individual to the next. For those who know me sorry for being

redundant I'm just trying to familiarize those who don't with the

difference in my condition.

I have been taking LDN since the last week in October of 05', (2

years and 4 months, except during hospitalizations and between

Rx's). Diagnosed with MS, (following numerous misdiagnoses), in June

9, 05' I knew I didn't want standard meds and fortunately found LDN

and finally this group. I began with liquid LDN (Revia) at 3mg until

I was able to obtain an Rx which I sent to Skip's. I asked my neuro

to increase the dosage to 4.5mg last spring following an MRI. She

noted though my MRI had not changed I appeared to have significantly

improved.

When I look back at 30 plus years of progressive symptoms which began

with falls, and odd pain, gradually increasing with episodes of

blindness by the late 90's, cognitive problems, slurred speech, lack

of energy, incontinence, chronic pain, recurring pneumonia, extreme

difficulty walking, lack of coordination, dropping things, losing my

voice for two months just prior to diagnosis, increasing vision

problems, MS Hug, sleeplessness from pain, daily spasms, and that

charming little drool, (I'm sure I'm leaving out plenty), the

difference is a miracle. All that is left of my MS symptoms are some

cognitive and vision problems; although walking tires me easily and I

have joint pain it can probably be attributed to one of my other

numerous ills which I hope will, in time, be eliminated or at least

curbed via continued use of LDN. I tell everyone who is willing to

listen, LDN is the most important drug since penecillin. I feel

Blessed every day for having found LDN and for all who encouraged me.

The 2007 LDN Conference was wonderfully informative and encouraging.

I was so happy to have been able to attend and finally meet so many

of you who helped teach me about LDN, answered my questions, and kept

me positive with your testimony when I went through rough spots.

Cyndi, Skip, Adam, Crystal, Aletha, , Jan, Jim and ,

Suzie, Dr. Gluck, Dr. Crowley, if only there had been more time to

speak with each of you and those who I'm sure I forgot to mention as

well, it was great meeting all of you. A fantastic job pulling it all

together ! I'm eagerly looking forward and hope to be able to

attend the next one as well.

Hugs, Prayer, and Laughter,

Gigi

[Guest guest]

Hi Gigi,That's great news about your tremendous improvement using LDN!I'm sure the LDN conference was great, too, and I'm very much looking forward to watching the conference video when it comes out.This site has helpful advice about options which may be of help in treating your residual MS symptoms:http://tinyurl.com/grpm9With best wishes,Dudley Delany

dudley_delanyFrom: georgina374

Sent: Tuesday, February 19, 2008 4:50 AM

low dose naltrexone

Subject: [low dose naltrexone] Update and more

Hi Everyone,

I planned to comment on the conference and update my progress on LDN,

then shortly after the conference I was hospitalized with a pulmonary

embolism for 11 days and have not been able to shake off the creepy

depression that followed me home from the hospital. I hope my post

makes sense and gives encouragement to any who have not yet seen

expected results. Please remember though it varies from one

individual to the next. For those who know me sorry for being

redundant I'm just trying to familiarize those who don't with the

difference in my condition.

I have been taking LDN since the last week in October of 05', (2

years and 4 months, except during hospitalizations and between

Rx's). Diagnosed with MS, (following numerous misdiagnoses), in June

9, 05' I knew I didn't want standard meds and fortunately found LDN

and finally this group. I began with liquid LDN (Revia) at 3mg until

I was able to obtain an Rx which I sent to Skip's. I asked my neuro

to increase the dosage to 4.5mg last spring following an MRI. She

noted though my MRI had not changed I appeared to have significantly

improved.

When I look back at 30 plus years of progressive symptoms which began

with falls, and odd pain, gradually increasing with episodes of

blindness by the late 90's, cognitive problems, slurred speech, lack

of energy, incontinence, chronic pain, recurring pneumonia, extreme

difficulty walking, lack of coordination, dropping things, losing my

voice for two months just prior to diagnosis, increasing vision

problems, MS Hug, sleeplessness from pain, daily spasms, and that

charming little drool, (I'm sure I'm leaving out plenty), the

difference is a miracle. All that is left of my MS symptoms are some

cognitive and vision problems; although walking tires me easily and I

have joint pain it can probably be attributed to one of my other

numerous ills which I hope will, in time, be eliminated or at least

curbed via continued use of LDN. I tell everyone who is willing to

listen, LDN is the most important drug since penecillin. I feel

Blessed every day for having found LDN and for all who encouraged me.

The 2007 LDN Conference was wonderfully informative and encouraging.

I was so happy to have been able to attend and finally meet so many

of you who helped teach me about LDN, answered my questions, and kept

me positive with your testimony when I went through rough spots.

Cyndi, Skip, Adam, Crystal, Aletha, , Jan, Jim and ,

Suzie, Dr. Gluck, Dr. Crowley, if only there had been more time to

speak with each of you and those who I'm sure I forgot to mention as

well, it was great meeting all of you. A fantastic job pulling it all

together ! I'm eagerly looking forward and hope to be able to

attend the next one as well.

Hugs, Prayer, and Laughter,

Gigi