Appears yes:

FDA-approved naltrexone, in a low dose, can normalize the immune system — helping those with HIV/AIDS, cancer, autoimmune diseases, and central nervous ...

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When it comes to diet for auto immune conditions it is so confusing.  All I was told that spirulina should be avoided if you have an overactive immune system so I avoid it.  Thanks for the photos!  Am now on 1.8mg of LDN and my sleep was bad last night, also all my teeth ache. My eyebrows are losing hair rapidly so going to have permanent makeup done on those for the time being.   Please keep me updated about your daughter and thanks for all your help! 

Please keep me posted. Did you join FB group OVERCOMING AUTOIMMUNE DISEASES WITH LDN? I have heard the sleep issue only lasts a few nights. We ramped up .5 per week. I will be thinking if you. :-)
No signs of any regrowth, hair still thinning badly and my eyebrows are terrible. On 2.1ml of LDN. Starting to panic that this won't work for me. It helps with my joint pain but am getting a very dry mouth.

You might want to increase dosage of LDN to 4.5 MG. That is the recommended dosage.

LDN has completely stopped my daughter's hair fall. The little blonde hairs are very faint and slow to grow. But they are there and her head is covered in them. They feel like smooth velvet when I rub them. She has had not a single side effect. Nothing. A proper pharmacy is of the utmost importance. It must be compounded into liquid form. Adults usually take 4.5 for a while before results come. There are two wonderful Facebook pages with lots of good info. One is GOT ENDORPHINS. The other is OVERCOMING AUTOIMMUNE DISEASES WITH LDN.
There is a woman on GOT ENDORPHINS with alopecia. She says LDN grew her hair back. If you are trying, please keep us posted. Could take 8 to 10 months for results.

all head? eyebrown and eyelashes? ...this cure is for all life or a time hairs back we can stop, thank you for your help.

She never lost lashes and brows. I believe LDN halted the progression from reaching that point. Hair was going very fast. The shedding has stopped. I am not sure about lifetime treatment. Since it is not toxic, I would be ok with that. Will be testing her C reactive protein again soon to see if inflammation is down. She was at a 12.2. Not good! If it is down I will know LDN is targeting the inflammation causing all the trouble. I will update when numbers are back.

pterese,

Please keep us posted. The more we learn about treatments the better. I have been on LDN about a month, too soon to see any results. I will certainly post results should I see any.

Sounds great. Would love to know. Can take 8 or so months.
It's great there is a few of us here regarding LDN. Let's all keep updating each other. Will up my dose to 3ml during this week. Am seeing my dermatologist tomorrow regarding my scalp biopsy(it is actually my rheumatologist who has prescribed me LDN) so will be interesting to see what he says. The biopsy report hinted at scarring alopecia despite being told constantly not to worry as my scalp looked healthy!?!? Now my eyebrows are disappearing - all so horrible! Big day tomorrow as god knows how I will cope if it is scarring! I also get my LDN at Dicksons pharmacy in Glasgow.
Are you following a protocol from your dr for raising dosage? .5 per week is the norm. We will be thinking of you. I know how stressful this is. Keep your faith.

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