Binkie4
Senior Member (Voting Rights)
An earlier thread
https://www.s4me.info/threads/ldn-seems-to-be-working.8936/
Edit: corrected thread
https://www.s4me.info/threads/ldn-seems-to-be-working.8936/
Edit: corrected thread
An earlier thread
https://www.s4me.info/threads/ldn-seems-to-be-working.8936/
Edit: corrected thread
Thank you. This was interesting!An earlier thread
https://www.s4me.info/threads/ldn-seems-to-be-working.8936/
Edit: corrected thread
Good to know. Thanks! I'm sorry it didn't work for you though.I was just taking it a while ago but I stopped because it didn't help at all. I took it for about 10 weeks, slowly working up from 1.5mg to 5mg. I used this website to figure out the duration. On that website Jarred Younger states that "it can take 8-10 weeks to determine if you will respond to the drug. Don’t stop taking it before then."
Thanks @andypants Interesting to hear your LDN journey. Glad to hear your pension got approved and that you're a bit stable at the moment. Good luck with your other health related projects!LDN was mostly helpful in reducing chronic, vague neurological pain for me. It might also have expanded my energy envelope a tiny bit, but then not feeling like every nerve ending is low key burning all the time would probably do that too!
I started slow and built up. The first 10 days or so the pain got worse, before suddenly getting better one day. I remember having more sleep issues during those first days as well. It did not help with the underlying causes but camouflaged the pain, so I had to remember that I still couldn’t do more even if I felt better most days.
I experimented a little with dosing and timing and eventually figured out that taking 0.5 mg morning, midday and afternoon worked best for me. The pain reducing effect would taper of after about 4 hours, so I spaced the dosages at approximately 4 hours apart but avoided anything in the evening as that would make it harder to sleep. Increasing dosages above 0.5 mg at a time made no difference (or possibly made the pain worse, I can’t reliably remember).
I stopped taking it after a year or so. I thought the effect might be wearing off and decided to take a break. A break also seemed like a good idea because my stay at the rehab clinic was coming up and I didn’t want to fool myself into thinking I could tolerate more than I could (especially with people encouraging you to participate). After the rehab I was too reduced and worried about getting approved for my disability pension and didn’t have the energy to get my prescription renewed. The cost was also an issue at the time since I was worried about not having an income very soon.
I got better and had my pension approved, but since I’m pretty stable atm and have other health related projects going I have not made the effort to get a new prescription. In summary I thought LDN was helpful, but not revolutionary. I might try it again later, if the timing is right![]()
Thank you. Sorry it wasn't very helpful for you. Seems clear it's not a wonder drug for most. Hope we'll learn more soon whether there might be a sub group that may have some profit from using it.I took 4.5 mg at night for a couple of years. Thought it was helping with sleep, perhaps mood and restless legs. When I went off it a few months ago to find out I did have more discomfort in my legs for about a week or two but then went back to normal. So I'd say if it did help for a while it wasn't helping any more. My impression is some people seem to report significant pain relief.
Maybe @Dechi - if they so wish - could give us an update a year after the LDN trial?
So glad to hear you feel it helps you @pteropus !! I can imagine that was a wonderful day to be out in the sunshine again after so long timei love my LDN. after GET & years of extreme photosensitivity - then very slow increments of LDN dosage, i was able to go outside in bright sunshine, without pain. blue sky, trees, birds flying, all the lovely things. it was a very happy day.
i started on 0.15mg, slowly worked up to 3mg, then (over years) up to 6mg. i've tried slightly higher doses, but not much additional benefit.
That sounds awful. Thanks for telling though. Good to be aware of! I'm sorry LDN wasn't for you.I tried it last year, started with 0.5 mg. While it interfered a bit with my sleep, I initially felt like I tolerated it and was hoping it would have a positive effect. Unfortunately I developed severe depressive symptoms after a few weeks and had to quit. I read up on that reaction and apparently a certain percentage experience depression as a side effect and the recommendation then is to stop taking it immediately.
So that was a bit of a bummer, but glad I tried it anyway, in case it would have worked for me. Good luck!![]()
You might find this FB group helpful: https://www.facebook.com/groups/200010163370187
I tried it last year, started with 0.5 mg. While it interfered a bit with my sleep, I initially felt like I tolerated it and was hoping it would have a positive effect. Unfortunately I developed severe depressive symptoms after a few weeks and had to quit. I read up on that reaction and apparently a certain percentage experience depression as a side effect and the recommendation then is to stop taking it immediately.
So that was a bit of a bummer, but glad I tried it anyway, in case it would have worked for me. Good luck!![]()
@Yessica I'm so sorry for your lossI read about LDN possibly causing that when researching LDN. That's one reason I didn't start it last year because some people I loved had died recently. I didn't think I could handle if any depression happened cause of LDN on top of mourning.
Thank you so much, @Yessica !Good luck @Kalliope, hope it helps you!![]()
I'm so sorry to hear about your loss. Agree with @Anna H it sounds like it was a wise decision to wait.I read about LDN possibly causing that when researching LDN. That's one reason I didn't start it last year because some people I loved had died recently.
It's about 6-7 weeks since I started with LDN. Not any big effects so far. Perhaps deeper sleep and less "burning" sensation in brain after concentration.Dreadful experience. Started on 0.1mg, then 0.2mg. Only managed 10 days as it made me very irritable and aggressive (I'm very patient normally),t unable to sleep more than 1 hour at night.
https://ldnresearchtrust.org/valari...-syndrome-cfsme-low-dose-naltrexone-ldn-storyValarie from the United States shares her Chronic Fatigue Syndrome (CFS/ME) and Low Dose Naltrexone (LDN) story on the LDN Radio Show with Linda Elsegood.
Valarie grew up knowing she has issues with her health but her symptoms were exacerbated when she joined a health club and tried to exercise more regularly. This worsened to the point where one day she could no longer get up out of bed.
After doing some research, Valarie found Low Dose Naltrexone (LDN) on Facebook and learnt of its many benefits for patients diagnosed with Chronic Fatigue Syndrome (CFS/ME).
“LDN has made me so much less anxious and stressed. I feel better about myself. I’m a very strong supporter of LDN and it’s definitely worth trying.
This is a summary of Valarie’s interview. Please listen to the rest of Valarie’s story by clicking on the video
Sure you can. Are you thinking about trying it too?Hi @Kalliope
Can I ask you, how did this go? Do you feel any changes?
Sure you can. Are you thinking about trying it too?