Re: Weird side effects on 3mg

[Guest guest]

>

> I have been experimenting with LDN for ALS and have been on 3mg. for

> only a few days. I was on 1.75 for ten days and other than vivid

> dreams I noticed no effect. Today I am very lame from last night and

> during the night it was apparent I was being affected by the LDN in

> the same negative way. I also had a few weird sensations which seemed

> to come from the nerve itself, something I have never felt with my

> disease. I have heard others talk about stiffness, but that is not

> what I would really describe my side effects like; more soreness and

> lameness upon awakening and during the night. Usually starting out

> the day is when I feel my best and not bad all things considered. Is

> this something others have experienced and do you think it will go

> away? I do not have the same level of assurance that LDN is effective

> in ALS as most of you do with MS assumming you are one of the lucky

> ones but I would like to know for myself and others if it may be an

> effective therapy for ALS. Please let me know what the more

> experienced here think. Also I do feel as though I had given the 1.75

> enough time for myself to adapt so I can't see going back down to

> that dose based on the prevailing opinion that it is too low to be

> helpful. Thank you.

=================

This may help. The same may go for ALS as does MS on LDN. Once you click on

the link scroll down past the ad.

Low Dose Naltrexone Forum - Why U may get increased symptoms in 1st 3mo on LDN

http://ldn.proboards3.com/index.cgi?board=forum & action=display & num=1104334920

[Guest guest]

>

> I have been experimenting with LDN for ALS and have been on 3mg. for

> only a few days. I was on 1.75 for ten days and other than vivid

> dreams I noticed no effect. Today I am very lame from last night and

> during the night it was apparent I was being affected by the LDN in

> the same negative way. I also had a few weird sensations which seemed

> to come from the nerve itself, something I have never felt with my

> disease. I have heard others talk about stiffness, but that is not

> what I would really describe my side effects like; more soreness and

> lameness upon awakening and during the night. Usually starting out

> the day is when I feel my best and not bad all things considered. Is

> this something others have experienced and do you think it will go

> away? I do not have the same level of assurance that LDN is effective

> in ALS as most of you do with MS assumming you are one of the lucky

> ones but I would like to know for myself and others if it may be an

> effective therapy for ALS. Please let me know what the more

> experienced here think. Also I do feel as though I had given the 1.75

> enough time for myself to adapt so I can't see going back down to

> that dose based on the prevailing opinion that it is too low to be

> helpful. Thank you.

=================

This may help. The same may go for ALS as does MS on LDN. Once you click on

the link scroll down past the ad.

Low Dose Naltrexone Forum - Why U may get increased symptoms in 1st 3mo on LDN

http://ldn.proboards3.com/index.cgi?board=forum & action=display & num=1104334920

[Guest guest]

Has your lameness and soreness continued or abated now?

endalsnow wrote:

I have been experimenting with LDN for ALS and have been on 3mg. for

only a few days. I was on 1.75 for ten days and other than vivid

dreams I noticed no effect. Today I am very lame from last night and

during the night it was apparent I was being affected by the LDN in

the same negative way. I also had a few weird sensations which seemed

to come from the nerve itself, something I have never felt with my

disease. I have heard others talk about stiffness, but that is not

what I would really describe my side effects like; more soreness and

lameness upon awakening and during the night. Usually starting out

the day is when I feel my best and not bad all things considered.