LDN (Low Dose Naltrexone)

[louisa]

Hoi allemaal,

Even een vraagje. Heeft iemand van jullie de Petitie Erken ME: http://petities.nl/petitie/erken-myalgi ... che-ziekte met toestemming van marja natuurlijk, op het forum hormonale disbalans kunnen zetten?

Dat forum wordt veel gelezen en misschien zijn daar ook mensen die de Petitie willen tekenen?

Groetjes, Louisa

[greta]

Van de LDN yahoogroup:



My husband was diagnosed with parkinson's about 1 month ago. His Neuro
dr was very adamant about LDN when I asked for his approval to prescribe
it for the disease, stating that it had no effect whatsoever on
Parkinsons and promptly handed us Azilect samples.

I had already done my
research but knew it would be a waste of time to carry the discussion
further. Thank God we were there only for the diagnosis then took that
to his pcp who is open to current research and alternative options-he
did prescribe it.

We obtained a 3 month script as per the following:
(1stmo/1.5mg)-(2nd mo.@3.0mg ) & (3rd mo.@4.5mg .).
So far he has been on LDN (1.5) for about 3wks and for the past few days his jaw has stopped trembling and his hand & arm tremors have quieted down.

I am elated!!!
Of course I must give Praise to The Lord as He is involved in this!!

[diederik]

Hm, dus GOd is de uitvinder van LDN! Dat verklaart veel.


(haleloeja )

[asje]

Ha ha. Maar wel interessant dat het deze persoon bij Parkinson hielp toch.

[diederik]

Tuurlijk dat


Vond de onderste zin gewoon zoo Amerikaans

[asje]

It sure is, vreselijk.

[greta]

Dat kom ik regelmatig tegen in de mails van LDN yahoogroupleden.
Maar er gebeuren dan ook vaak wonderlijke dingen met LDN gebruikers

[greta]

Eigenlijk zou ik dit misschen wel vaker met jullie moeten delen.
deze bv:

I have been using LDN 3mg dose since a half year. I was suffering coz of Ankylosis which made my life terribly worst due to sacroiliac and spine pains.. However, LDN has worked after 3-months time and I am mostly feeling great since 2-months.. I am also keep on using Wobenzym-Plus and Omega-3 (3000mg) together with LDN..

Thanks all for sharing and made my life better..

Cheers,
Peskir

[greta]

En deze:

Barb Washicosky 7 november 0:25

Well got to tell everybody, I have been on LDN for about 3-4 weeks, For the first time in about 8 months the puffiness and swelling in my eyes has started to go down, and my sinuses seem a tad clearer..Hope it keeps working...LOL

[greta]

En deze;

I am happy to say with in 6 weeks my IBS was totally under control. .. I got to enjoy summer fruits and my fave watermelon all summer long with out having to spend the day in the bathroom!!!

----- Original Message -----
From: Bonnie Seibert
To: lowdosenaltrexone@yahoogroups.com
Sent: Friday, November 11, 2011 2:44 PM

[greta]

En deze:

Yes, I have both MG and Lupus and have responded remarkably from the LDN; have been taking 4.5 mg for 2-1/2 yrs. and have not had any flares of disease for that long it has virtually put me into remission, giving me more energy than i've ever had before! but, more importantly, no flare of weakness anymore and no more prednisone!
Darlene

[greta]

En deze van een MS patiente:

Luckily I found LDN and it has improved my bladder functions, leg spasms, energy level, which is up. No more fatigue and I believe progression has stopped, though occasionally when I struggle (I do limp and lose balance quite a bit) I have fears that maybe there is something going on, but I have to tell myself, that despite LDN I still get older, I am menopausal, and chances are, that I do a heck of a lot more now than I did three years ago. No surprise then if I get tired!

LDN is fabulous, it's given me hope for the future, where at the time of diagnosis there was just despair. And I've not had a cold since LDN either! YES!

Silvia (PPMS, LDN for 33 months)

[ldn-ster]

Ik zou jullie graag willen wijzen op de nieuwe Facebook groep 'LDN gebruikersgroep Nederland'

Als je LDN gebruikt, ben je van harte welkom. je kunt hier ook snel en makkelijk ervaringen en tips uitwisselen met andere mensen die LDN gebruiken.

Binnenkort zal er ook weer nieuwe info verschijnen op www.lowdosenaltrexone.nl

Groet!

[greta]

Er is ook een engelstalige LDN/ME/CVS facebookgroep
http://www.facebook.com/permalink.php?s ... 163370187/

[greta]

Van een andere facebookgroup:

Helen O'Neill
I have been taking LDN for nearly 3 years for CFS/ME with brilliant results...I would thoroughly recommend it for any immune related disease

http://www.facebook.com/#!/groups/LDNRT/