You should start at .5 and slowly ramp up to 4.5mg. Add .5 each week.
...how did your stories with low dose Naltrexone ever continue!?
I also have AU and just heard of this for the first time...
And am curious...thanks for sharing!
I was hoping to see some more posts from pterese about her daughter. I have had Alopecia Totalis for a year. I started LDN about 45 days ago and I'm pleased to say that I have little vellus hairs all over my head. I'm also using minoxidil 7% with a steroid topically twice a day. I really feel that it's the LDN that's making the difference. I have changed my diet to gluten-free, dairy-free and very little sugar. I take a number of supplements, including 5000 mg of vitamin d a day and 1500mg of vitamin a. I'm not very good at taking selfies but here's how it's looking so far. I will keep posting updates. It might be hard to see the hairs but they are there!
Interested to hear too how others are getting on with LDN. I stopped it for a while along with plaquenil as I was becoming allergic and we had to find out what I was allergic too. I am now restarting LDN. However during the year I was on LDN I didnt get any hair regrowth but I am now planning to take LDN in isolation so maybe that will help. Also anyone have very dry, matt, ridged nails too?
Hi, yes I tried this for one year and had very little growth which disappeared shortly after stopping use of it.sorry I don’t have better news
I started my treatment with prEp. It is the most innovative drug at the moment. I tested for HIV two years ago. It was difficult for me to accept my life sentence, but I somehow overcame this period. Blessed that my parents were by my side and were supported. I have received the government's support by providing a free and anonymous platform as pinknews.co.uk There are doctors you may consult, and they give you the right prescription, and the delivery of the medicine is right away at your door.