Guest guest Posted March 12, 2011 Report Share Posted March 12, 2011 Have been taking LDN for about 2 1/2 weeks - do not feel any change yet - still stiff and heavy/tired. I have PPMS. Does anyone have this type of MS who has seen good results? Thanks, in advance. Jane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2011 Report Share Posted March 12, 2011 Hi Jane. I don't have ur diagnosis but have read of many that do and def see results. So def keep taking. It'll happen where the bigger issues will show improvement and smaller annoyances will subside w/o u noticing. For me, like most every1 saw a slight increase of symps which is scary as hell. But after that improvement. While I've read that sum do notice sum improvement immediately, I think 2 weeks is too soon to gauge. Just consider that it does 2 things (well more obviously) stop disease progression and altho not guaranteed, relieve symps. I don't know for sure but it makes sense to me that it wud cease progression 1st then work on cleaning up those messy symptoms. Stay at it. HUGS. From: Cimini <dcimini3@...>; To: <low dose naltrexone >; Subject: [low dose naltrexone] LDN PPMS Sent: Sat, Mar 12, 2011 7:46:42 PM Have been taking LDN for about 2 1/2 weeks - do not feel any change yet - still stiff and heavy/tired.I have PPMS. Does anyone have this type of MS who has seen good results?Thanks, in advance. Jane------------------------------------ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2011 Report Share Posted March 12, 2011 Jane What happens with people with MS is usually no further progression. So you may not feel any different! That would be good! SOME people get some symptom relief but not all - really the idea is not to get any worse. Good luck and stick with it.Bev low dose naltrexone From: dcimini3@...Date: Sat, 12 Mar 2011 14:46:42 -0500Subject: [low dose naltrexone] LDN & PPMS Have been taking LDN for about 2 1/2 weeks - do not feel any change yet - still stiff and heavy/tired.I have PPMS. Does anyone have this type of MS who has seen good results?Thanks, in advance.Jane Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2011 Report Share Posted March 12, 2011 This would be a good read for you: Topic: U may get increased symptoms in 1st months on LDN http://ldn.proboards.com/index.cgi?board=forum & action=display & thread=148 I had increased stiffness (tonic spasm) in the first month on LDN. Later LDN increased clonic spasm when I tried to raise the dose. It helps to know that others have also experienced this. At 9 months on LDN, I rarely have any spasms at all. I suggest hanging in there for the long run and hope for the benefits. K.C. > > Have been taking LDN for about 2 1/2 weeks - do not feel any change yet - still stiff and heavy/tired. > I have PPMS. Does anyone have this type of MS who has seen good results? > Thanks, in advance. > Jane > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2011 Report Share Posted March 13, 2011 229 experiences of ms with ldn https://ldndatabase.dabbledb.com/page/cancer-researchcopy/ddXxiaHj# also ppms I am using the Free version of SPAMfighter.SPAMfighter has removed 2299 of my spam emails to date.Do you have a slow PC? Try free scan! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 13, 2011 Report Share Posted March 13, 2011 hi jane, me to primary progressive and lucky can now get scrip from doc/nhs that i mail to dicksons started low 1ml[solution] and now on 4th month on 4.5ml [capsules] after approx 3 months improvement in fatque, bladder, bowels, brain fog, depression mistake i made was coming off the baclofen as i suffer from severe legs stiffness, cramps, spasms stick with it as long term gain regards/peter Have been taking LDN for about 2 1/2 weeks - do not feel any change yet - still stiff and heavy/tired.I have PPMS. Does anyone have this type of MS who has seen good results?Thanks, in advance.Jane Quote Link to comment Share on other sites More sharing options...
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