Jump to content
RemedySpot.com

LDN

Rate this topic


Guest guest

Recommended Posts

HI Tom,

Is the LDN expensive? I don't have any insurance and as of yet no medicare or

medicaid since I am still waiting on the hearing for my disability.

Regards, Bonnie

>

>

> Date: 2003/09/25 Thu PM 01:49:08 EDT

> To: MSersLife

> Subject: Re: LDN

>

>

Tom,

I'm so curious about LDN. I have visited the website. I'm wondering

how many members of this group are on it. Maybe I'm just looking for

anything that will get me off the interferons because I believe they

contribute to the fatigue that has impacted me so heavily. I know

everyone is different but fatigue has seriously changed my life. I'm

not working which some may see as a good oppty to pursue other things

but I don't have ANY energy to pursue other things.

Can anyone take this med? Is it considered experimental? If so,

insurance won't cover. Thanks for any feedback.

-- Jackie

> Hi Bonnie,

> No, I do not take any other meds. The only meds that would

conflict with LDN are opium derivative drugs.

> Regards,

> Tom

> LDN

> >

> >

> > Dear Tom,

> >

> > You may recall that I belong to the yahoo chat

group....trying to keep posted on what is working for MS for a friend.

> >

> > I have followed your situation with LDN, and I wonder if you

would kindly post an update. How are you doing today? How long has

it been? Have you done anything else significant, the effects of

which might also be contributing to your status.

> >

> > I would so much appreciate this...and thank you kindly for

your caring and sharing.

> >

> > Best regards,

> >

> > Grayce Stratton

> >

> >

> >

> >

>

>

>

Link to comment
Share on other sites

  • 3 months later...

oh tom! there´s no problem with the Govern!

wud u do it 4me? it wud be great!

how can I pay 4it? I don´t know about these stuffs! but I can learn if u teach me!

oh plz! he disappeared b4 starting it to me!

Regards, Andreia XXXXX

visit my web page and sign my guest book:

http://msmemoriesandthoughts.bravehost.com/

Re: LDN

Andreia,

Maybe one of us could have it shipped or mailed to you. Would that cause you any trouble with the local authorities ?

Regards,

Tom

Link to comment
Share on other sites

Hi Andreia,

Try to contact one of the doc's on the following list. If he prescribes it you could have the pharmacy send it to you.

Regards,

Tom

Dr. Bernard Bihari New York, NY Dr. Sidney, NY Dr. Carole Saratoga Springs, NY Dr. Stafford Colorado Springs, CO Dr. Bruce Sharpnack Hickory, PA Dr. Jeff Esper Erie, PA Sullivan Mechanicsburg, PA Dr. Patti Townely Dwight, IL Dr. Myers Skokie, IL Dr. Alan Buchman Chicago, IL Dr. Bernard s Vernon Hills, Illinois Dr. Stanley Knep (Neuro) Clifton, NJ Dr. Wisconsin Dr. ph Wezensky, MD, GP Dr. Rick Jensen, ND Kokopelli Health & Wellness Grand Junction, CO http://www.acam.org/dr_search/ Dr. search www.lef.org search of innovative DR.

Link to comment
Share on other sites

ty Tom. I will try to contact ACAM(the site) and email it cos I really can´t speak up English but I can write!

I do hope it works!

fingers crossed!

Regards, Andreia XXXXX

visit my web page and sign my guest book:

http://msmemoriesandthoughts.bravehost.com/

Re: LDN

Hi Andreia,

Try to contact one of the doc's on the following list. If he prescribes it you could have the pharmacy send it to you.

Regards,

Tom

Dr. Bernard Bihari New York, NY Dr. Sidney, NY Dr. Carole Saratoga Springs, NY Dr. Stafford Colorado Springs, CO Dr. Bruce Sharpnack Hickory, PA Dr. Jeff Esper Erie, PA Sullivan Mechanicsburg, PA Dr. Patti Townely Dwight, IL Dr. Myers Skokie, IL Dr. Alan Buchman Chicago, IL Dr. Bernard s Vernon Hills, Illinois Dr. Stanley Knep (Neuro) Clifton, NJ Dr. Wisconsin Dr. ph Wezensky, MD, GP Dr. Rick Jensen, ND Kokopelli Health & Wellness Grand Junction, CO http://www.acam.org/dr_search/ Dr. search www.lef.org search of innovative DR.

Link to comment
Share on other sites

  • 7 months later...
  • 5 months later...

In a message dated 1/19/2005 3:33:36 AM Central Standard Time,

Ive been on it 4 months, Karin, and saw improved energy the first day--also

less " tight " feeling in my R Leg the first morning--has continued ever since

and I'm one of the lucky ones who also am having some symptoms reverse--lots

of the numbness in my feet and legs is gone. I have had very few side

effects--some interrupted sleep at first, and some really vivid dreams (not

nightmares, though) for a few weeks. I was on Copaxone for a year and though I

didn't have to (you can do Copaxone and LDN at the same time) I was getting

side

effects from Copaxone so decided to just get off it. I really recommend it

and there are lots and lots of others doing it for MS as well as other

autoimmune diseases and even Cancer at the LDN group:

_lowdosenaltrexone _ (mailto:lowdosenaltrexone )

You sign up for that

group the same way you did this one.

I don't understand why anyone would start with the very low dose of 1.5 mg

when 3.0 or 4.5 is the amount recommended by the doc who started the whole

thing. Unless a person is extremely drug sensitive, I'd start at either 3.0 or

4.5mg You take it between 9 pm and 3 am whether you're sleeping or working

the nite shift--pretty darned easy & cheap.

Daphne

mscured writes:

Please, those of you that are on it tell me very specifically what it has

done for you? How are you taking it? have you heard that " slow release " LDN

is not good? What side effects have you had? Any medical problems as a

result from LDN?

Link to comment
Share on other sites

  • 2 weeks later...

Interesting stuff. Keep in mind this won't force the FDA or MSS to do

anything, but imagine the egg on the MSS's face if trials prove it to

be effective. It takes the Vermont HR to point out to the MSS that

LDN warrants more research. Perhaps I should my donations to them.

.......

>

>

>

--------------------------------------------------------------------------------

> RESOLUTION AS INTRODUCED 2005-2006

>

> State of Vermont

> House of Representatives

>

> Montpelier, Vermont

> Joint House Resolution

>

> J.R.H. 6

>

> Joint resolution urging the Food and Drug Administration and the Multiple

Sclerosis Society to study the efficacy of low dose naltrexone as a multiple

sclerosis medication

<snip>

Link to comment
Share on other sites

  • 4 weeks later...

I just got off the phone with Skip, from Skip's Pharmacy in

Florida. We had a long discussion about LDN. He said that in some

cases it's very helpful for reglating the cells around lesions,

keeping them from attacking the myelin sheath on the edges of an

existing scar. He said that exacerbations of MS happen when there

is new activity there (around the edges) and that if the center of

a lesion is scar tissue, it can't be reactivated. The lesions can

spread from free-radical activity (when the cells attack good tissue

instead of bad) and LDN regulates this actvity. LDN won't bring

activity back from a scarred area, but will prevent further

spreading of the scar in some cases. It doesn't help with bladder

control unless a lesion in that area of the brain is flaring-up. The

same is true with mobility. It does nothing for muscle cramping.

My question to you is, what effects have YOU seen with LDN?

According to Skip, he sells over 100,000 prescriptions per month. He

doesn't always get feedback from his customers to know all their

results.

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...