Morning Toni
I unlike Guppy feel that a biopsy is the only way to be completely sure it is LS
Of course the consultant who did not even take time to examine you is appalling !! It is not only the physical side of things that has to be addressed but your mindset as well
To get syched up for consultation is hard enough. Tell me Toni was it a man or a woman ? Also your first meeting Disgraceful
Anyway, I was diagnosed nearly 16 years ago by biopsy There had been no architectural changes then, and I did not know what I was dealing with
The treatment has not changed in decades simply because there is No research into this
sneaky silent, often painful n itching ugly 👹 condition
This forum is probably the most informed Army of woman who can discuss their vaginas condition freely 👯♂️👯♂️👯♂️👯♂️ and can make a difference to people who are diagnosed with LS and take away anxious worrying feelings by being there and supportive.
Toni the best things I have to help me manage LS successfully
Is my portable bidet (❤️ It ) and 20 Mule Team Borax (There is a a link to tell you about the benefit of Borax and LS but I don’t know how to do it ) 🙄
Betnovate ointment in case of flare up and coconut oil for moisturiser. Talk about DIY interest in my Ladyship !!!
I live in Warwickshire and my consultant is Prof Sean Kehoe in Birmingham and he is the most honest specialist I have ever met
He told me LS does not cause cancer but cancer can cause LS !!
quite frankly Toni we know more than any of ‘ em
I hear horrendous stories re LS but we have to remain calm and try to be logical with opinions we hear.
One mans meat and all that. You know what suits one ‘Ladyship’ Might not suit another !!
We living with it 24/7
Also, sorry to go on but this is my thought for the day 😂
I have over time changed my diet
Taken out sugar, dairy ( both big no no as far as LS concerned. As both heat bodies and LS loves hot
Alcohol also but hey ho two outta three ain’t bad 🎶🎶🎶
Sending ❤️
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