Has Anyone Been Suggested To Try Low Dose Naltrexone To Help Manage ET ? .. My GP Who Is Very Integrative Has Suggested This.
That seems like an odd thing to prescribe for someone with ET. Naltrexone is customarily used to treat someone who has been addicted to opioids, or to those with things like fibromyalgia or chronic pain syndrome. It is anti-inflammatory treatment for the latter.
I did use it (LDN) for a while but did not notice any positive effects on my platelet production or overall wellbeing
I continue with aspirin, vitamin supplements & maintain a reasonably healthy lifestyle.
I don’t know how old this thread is but there is interesting developments in the off-label use of LDN, specifically in the treatment of fibromyalgia and chronic fatigue syndrome. Also, it is being used in post-viral conditions such as long COVID to alleviate inflammation and a strange internal tremor (from which I suffer). All things being equal, I am looking at starting LDN to treat the tremors and am hopeful that it will also have a beneficial effect on fatigue and inflammations that come along with my PMF.
I would be interested to hear if your started it @A myMPNteam Member and how it goes for you.
https://www.verywellhealth.com/low-dose-naltrex...
https://www.verywellhealth.com/low-dose-naltrex...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10...
LDN isn't the same as Naltrexone. It's all in the dosage!. LDN has been very successful in the treatment of CFS/ME etc.
Interesting…I’ve heard of it being used with Chronic Pain.
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I'm 34 Having Myelofibrosis Grade 2. I'm On Jakavi 20 Mg For 6 Months. Initially It Was Good But Now My Platelets Are Rising Again At 700000