NeuroTalk Support Groups

NeuroTalk Support Groups (https://www.neurotalk.org/)
-   Multiple Sclerosis (https://www.neurotalk.org/multiple-sclerosis/)
-   -   LDN Information & Check-in 2 (https://www.neurotalk.org/multiple-sclerosis/71392-ldn-information-check-2-a.html)

SallyC 04-08-2015 10:22 AM

Quote:

Originally Posted by Kitty (Post 1134367)
I know the doctor we used to use retired. Who is prescribing your LDN now?
I might be ready to give it another try..........

I talked my PCP into prescribing it for me.:D
I had to assure him that the 4,5mg was pure Naltrexone powder w/filler,
compounded by Skips and not the bigger Rebia pills cut down. His
computer wouldn't allow it to go through as the cut down pill????

linter 04-14-2015 02:54 PM

Quote:

Originally Posted by SallyC (Post 1134305)
Anyone else? Am I almost alone here now?:eek::D

well, i have CIDP and just started LDN a week ago, using the disolve-the-pill method. don't really know what to expect but i thought i'd give it a shot and see if anything develops on the plus side.

i wake up to pee around midnight and take my dose then. afterwards, i've been having great vivid far-out dreams and i kinda like LDN just for that.

hopefully, more goodness will follow.

BioBased 07-13-2015 04:56 AM

I started LDN last week for CRPS. I think it is starting to help. I could not climb stairs, I had to sit climb for the past 5 months, after taking the LDN for a week I found I could walk upright on the stairs holding on to both rails. It still isn't normal stair climbing by any means, but it is progress. I also feel as if my extremities are waking up and I feel slightly more energetic.

Kitty 03-10-2016 05:48 PM

Received this in an email from LDNScience.org today:


LDNdoctor.com has been offering telemedicine LDN prescriptions for US residents for the past 5 months with great success. This makes getting an LDN prescription easier than ever.

If you prefer visiting a doctor for an LDN prescription, you may find a doctor by using our LDN Doctor Directory on our newly redesigned site: www.ldnscience.org


For the most trustworthy LDN information visit ldnscience.org

SallyC 03-11-2016 11:04 AM

Thanks Kelly/Kitty. I haven't been on LDN since I've been in the home.
I don't know if that is effecting my MS progression or not. It might be,
Because it was my savior for over 12 yrs and now I am not doing so well.

I may do well to go back on it?

I hate not being home and taking care of me.:mad:

caroline2 08-10-2016 04:47 PM

Just got this info on Scottish MD and LDN treatments. Lots of good reviews at end of article too;

Hearing told a Scottish GP has "a desire to help patients which needs to be kept in check" (From Herald Scotland)

caroline2 05-10-2017 08:25 PM

Any comments from those taking LDN? it's been a while since the above post was made. C

Twinkletoes 07-07-2017 09:46 PM

I took it for maybe 2 years. Quit a few years ago and haven't noticed any difference.


All times are GMT -5. The time now is 02:15 AM.

Powered by vBulletin • Copyright ©2000 - 2024, Jelsoft Enterprises Ltd.

vBulletin Optimisation provided by vB Optimise v2.7.1 (Lite) - vBulletin Mods & Addons Copyright © 2024 DragonByte Technologies Ltd.