Here for any guys needing support
Posted , 6 users are following.
Many of you have talked to me before im a 35 year old male living in Belfast and I was diagnosed with LS over a year ago and my foreskin is now back to almost normality , anyone needing any support feel free to get in touch
Eamonn
2 likes, 13 replies
mary_lou60460 eamonn58740
Posted
Very happy for you Eamonn.
Being a woman, i am curious what causes you to have a flare up?
eamonn58740 mary_lou60460
Posted
i wish i knew what caused it to flare but to be honest ive been lucky with flareups at its worse the whole underside of my foreskin was scar tissue
britbeth11 eamonn58740
Posted
When you say scar tissue "was" on the underside of your penis, are you saying that the tissue has healed or did you have surgery to remove it?
patricia87844 eamonn58740
Posted
hello Eamonn, do share, what miracle drug did you use? i am a woman and have had this problem for over 9 months now. No recovery in sight, any help most appreciated.
eamonn58740 patricia87844
Posted
no miracle drug unfortunately Patricia, i was misdiagnosed for over two years which caused the whole symptoms to get much worse. what i did that seems to work for me was to try and watch my sugar intake, ive been having Himalayan pink salt baths a few times a week and drug wise, cetraban as a barrier cream, washing with dermol lotion and now down to twice a week application of dermovate ointment . Hope that somewhat helps
britbeth11 eamonn58740
Posted
Eamonn, I have been searching the Internet for a male forum on LS. My husband (age 38) has been experiencing symptoms for a year now and after going to dermatologists and allergist and two urologist has was diagnosed by the second urologist. He has swelling and scare tissue and is circumcised . The doctor prescribed a steroid cream that was prescribed a few months ago by the dermatologist who told him to only use it for a week twice a day. Obviously didn’t do too much to help. His new urologist told him to use the cream every day twice a day liberally for two months and then we will go back to see him. I am seeing others talking about Manuka (sp?) honey and things they have used that help. We are desperate to get our sex life back to where is was and avoid any further complications . Sorry if this is TMI. Any and all advice you might have would be greatly appreciated. Could you also point us towards a forum specifically for males with LS ? would love to hear your story. Needing some help and encouragement.
britbeth11
Posted
Wow. So many typos and spelling mistakes in my post. So sorry! haha
Wee_Dugie britbeth11
Posted
Hi Britbeth, I can fully understand that the two of you are desperate to get things back as they were before, but as I explained on the Male Forum on this site, the fundamental is getting the correct healing process in place first, then you have a strong 'platform' or basis of much healthier skin on which to build from.
Unfortunately, the healing process takes time - this means a bare minimum of anywhere of 5 months and onwards, once the correct treatment regime is in place. Essentially, don't see the likes of Manuka Honey as a 'quick fix' - as, as I have mentioned - and certainly if you read the Forums here, what works for one person, can cause a raging flare-up for another person!!! This is why getting the correct Steroidal treatment working as best it can is essential.
I do not know what Eamonn would suggest about your remark to me about the surgery you mentioned. I see from the post here that your husband is circumcised. Do you know that the Medical Professional generally recommends circumcision for men with LS as a 'so called cure'?
Therefore, was your husbands circumcision done relatively recently?
Wee_Dugie eamonn58740
Posted
Hi Eamonn, I am a male who was diagnosed with LS almost 8 years ago. Just checking, but are you aware of the posts by Nancy KB on here? In particular, her post on 'Route into LS and the Protocol for dealing with LS'?
It has been mentioned by other males on here about starting a Forum, potentially on the "Penis Disorders" part of this web site, is this something you have considered either setting up, or being part of on a regular basis? I mentioned Nancy KB because, obviously, this would be one of the main potential resources a Male Specific Forum could draw on as a resource to give fellow suffers a basis on which to work from.
What do you think ..... ?
al22071 Wee_Dugie
Posted
do you have a link for Nancy KB
Wee_Dugie al22071
Posted
Do you mean so that you can contact her in person - or for you to view the most important information she has posted online elsewhere on this web site?
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For the benefit of future readers here are the links to the most essential information that Nancy has posted with regard to Autoimmune Conditions, with specific relevance to those with Lichen based Skin Disorders such as BXO / Lichen Sclerosus:
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https://patient.info/forums/discuss/nutritional-support-protocol-for-autoimmune-diseases-636963
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https://patient.info/forums/discuss/pathway-into-and-out-of-autoimmune-diseases--661033
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I also include a Link to a Response Posted by Starlight8 as I have found that the information is particularly relevant to dealing with Genital Skin Disorders where treatment consists of topical application of Steroidal Ointments - and again is most relevant to those dealing with or suspect they may have Lichen based skin disorders, such as ichen Sclerosus (LS):
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https://patient.info/forums/discuss/lichen-is-taking-my-life-need-help-660159?page=0#3199398
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.. for those accessing the final link you may need to scroll down the page to see the resonse posted by Starlight8 as it was not her original Forum Posting, it was a very detailed Reply to someone else.
Wee_Dugie
Posted
typo error - where I state: " ichen Sclerosus (LS) "- it should obviously read:
Lichen Sclerosus (LS)
al22071 Wee_Dugie
Posted
nice one