Rightsaidfred
Well-Known Member
Hi all
It's been some time coming but through popular demand, I have set up a new thread all about female hair loss.
This thread should remain professional, caring, informative and sensitive for anyone who reads and posts so please, no abuse. We are all women who should support one another.
I discovered I suffer from FPB (female pattern baldness) about 2 years ago, After noticing my parting was becoming wider. For me, the concentration is more around the very front top part of my fringe. I'd love to wear my hair in a centre parting but it just shows too much where my hair has reduced over time.
After much research and many blood tests, I discovered that there is no cure for this condition but there are options to help reduce the hair loss further. For my situation, it is also hereditary as my mother suffers the same as well as a cousin of mine.
So, what is this product that can help with FPB? It is a product called Minoxidil. You can get this over the counter in Boots and I use the 5% solution. It is a topical solution which needs to be applied onto dry scalp in the morning as well as in the evening for the rest of your life. Has it worked? Most definitely I can see a difference after using it for two years but, I wouldn't go as far to say that I have a new head of hair. It certainly does reverse the condition a little but it can get quite frustrating having to apply it twice daily. The problem with this solution, if you stop using it then your hair will start to fall out at the rate it was before. Ive learnt from much research that for every growth cycle, women with this condition find out that their hair follicle closes up which effectively stops the new hair from coming through thus, leaving you with a reduced amount of hair. I've heard of a laser comb which I have yet to try and at a mere £250 a comb, I'm not sure I could justify spending that sort of money on a gadget that hasn't had a huge impact on customers.lets open up the discussion.
Does anyone else suffer and if so, what did they find out about the condition and any treatments that have worked?
It's been some time coming but through popular demand, I have set up a new thread all about female hair loss.
This thread should remain professional, caring, informative and sensitive for anyone who reads and posts so please, no abuse. We are all women who should support one another.
I discovered I suffer from FPB (female pattern baldness) about 2 years ago, After noticing my parting was becoming wider. For me, the concentration is more around the very front top part of my fringe. I'd love to wear my hair in a centre parting but it just shows too much where my hair has reduced over time.
After much research and many blood tests, I discovered that there is no cure for this condition but there are options to help reduce the hair loss further. For my situation, it is also hereditary as my mother suffers the same as well as a cousin of mine.
So, what is this product that can help with FPB? It is a product called Minoxidil. You can get this over the counter in Boots and I use the 5% solution. It is a topical solution which needs to be applied onto dry scalp in the morning as well as in the evening for the rest of your life. Has it worked? Most definitely I can see a difference after using it for two years but, I wouldn't go as far to say that I have a new head of hair. It certainly does reverse the condition a little but it can get quite frustrating having to apply it twice daily. The problem with this solution, if you stop using it then your hair will start to fall out at the rate it was before. Ive learnt from much research that for every growth cycle, women with this condition find out that their hair follicle closes up which effectively stops the new hair from coming through thus, leaving you with a reduced amount of hair. I've heard of a laser comb which I have yet to try and at a mere £250 a comb, I'm not sure I could justify spending that sort of money on a gadget that hasn't had a huge impact on customers.lets open up the discussion.
Does anyone else suffer and if so, what did they find out about the condition and any treatments that have worked?