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Nov 28 07 1:12 AM
Your posts are offensive to many of us using calosol.
Perhaps you will be pleased to know that we are a family glad to be using calosol and thank God we did. This is our story in brief.
Our son is 12 and started loosing his hair January 2006 he only had three small patches and our GP said do not worry and his hair would grow back, he gave us a
steroid cream to use. The steroid creams did not help and more and more patches appeared on the scalp and also on the eyebrows, the Doctor referred us to a
Derm and by the time the appointment was made our son had lost 50% of his hair the left eyebrow and half of the other eyebrow. The derm offered us steroid
injections which were of no value apart from three new hairs regrown and lost soon after we stopped the injections. We decided to stop the injections when the
derm said that there was nothing more he could do, he also said that it was almost certain that our son's hair would never regrow. We were devastated to
hear this. By now the alopecia had progressed to 90% scalp loss.
We decided to start using the calosol after we got in touch with a mum that told us about their experience and success of complete regrowth using calosol on
their daughter's scalp . We started using the Calosol in October 2006 and within few weeks we started seeing tiny new fluffy baby hair all over his scalp.
We have now 95% regrowth and we cannot thank Elias enough. Elias wants us to continue until our son has a full head of hair. He has been very supportive and we
are very grateful for his help.
I hope Elias may live long and prosper, and continue with his work.
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