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Vitiligo cure success rate-Dr. Deoshok Sharma-success rate of Melanin LM4? & pros and cons? please 3

 

 

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The ABC Homeopathy Forum

Vitiligo-Dr.Deoshok Sharma-Melanin LM4

You said Melanin LM4 does not regenerate Malanicyte in the skin. Well what does it do? When I asked does GNC Cell Protector and Pycnogenol(50mg) the amino acid, L-Phenylalanine and Tyrosine restore Melanin in the skin. And also you said that Psoralia carliforia, Ars. Sulph Flab, oil bouchi, melinocyte cream does not work either.
You said,there is no drugs which can regenerate the malanicyte cell. So, how does the Melanin LM4 work and is it permanent of temporary? Is there studies to back these claims or your claims that Melamin LM4. I know there are many people out there with vitiligo who are tired of trying everything and nothing working. Please help us with the facts.
 
  mwmwmw on 2007-05-19
This is just a forum. Assume posts are not from medical professionals.
first you try . other wise I will give the phone no. and photogrphs of the patient you can enquire your self.

Here I am not challanging any thing in the medical.

Some time same disease may fail . There is no any gurantee of any disease. You may try .

dr.deoshlok sharma
 
deoshlok last decade
Have some of your cases of vitiligo spread? Is it possible do to using a drugs that is made from the disease. Please let me before using the pros and cons.
 
mwmwmw last decade
Dr.Deoshok Sharma,
Thank you for your quick reply always. I hope your are understanding to my many questions.
Yes, I would like to see photos. You are saying some time using the same disease may fail. Ok, but in some cases does it spread even more. What is the ratio of people getting cure with Melanin LM4? Please let us know the pros and cons of taking this medicine. Also is this a all natural medicine and have people had any reaction/ side effects to it? . Please let me know all the pros and cons before using? Yes, I would like phone numbers ,email addresses,and photos. Thank you for all your help. I hope you understand my concern with this disease. Me and many others have tried many other medicines and nothing is worked and this is frustrating and stressful having to hold on to hope for 3-4 months on each and every different medicine that fails. It is very time consuming months turn into years of holding on to hope. Also very expensive too. The disease is stressful in itself and to have so many failure on top of the disease is the worst. Please be understanding in helping people with this disease. Please us know if you think this will help us. How to purchase it and how much? Before we all go through this long haul again and again. Please answer all my questions
Thank you,mwmwmw
 
mwmwmw last decade

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