Introduction
Alright, beautiful soul. The holidays are quickly approaching. With that, I decided to write a post about coming out to friends and family with Lichen Sclerosus. Lichen Sclerosus is an incredibly isolating disease. Many of us go months or years feeling like we are the only ones in the world living with LS. Because vulvar Lichen Sclerosus affects the genitals, it can be really difficult to open up to friends and family about our diagnosis. However, I have spoken to many people with Lichen Sclerosus, and this not telling others about their Lichen Sclerosus is not for a lack of wanting. In fact, many people expressed a strong desire to tell friends and family about their Lichen Sclerosus, but they have no idea where to start. Thus, this post will focus on just that by providing some tips and tricks with respect to coming out to friends and family.
Don’t forget to read until the end for this week’s #TLLCTuesdayTip.
Dealing with Lichen Sclerosus on Your Own
When you are diagnosed with Lichen Sclerosus, it can literally feel like the wind is knocked out of you. You may feel a whirlwind of emotions. For example, you may feel stunned, scared, relieved, angry, confused, or sad. Further, you may completely dissociate (which is what happened to me when I received my Lichen Sclerosus diagnosis). Read my diagnosis story here.
Early in my Lichen Sclerosus journey, I didn’t know a single soul with LS other than myself. When I was diagnosed, my doctor informed me it was a disease that primarily affects post-menopausal folks and that I was an outlier. (I have since learned this is false, but I digress). This made me feel incredibly alone. I felt like an alien, a massive oddity in a sea of folks with normal, healthy vulvas.
It is quite common to suffer in silence for years with symptoms before finally getting diagnosed, and, similarly, quite common to then deal with Lichen Sclerosus completely on your own once you are diagnosed.
However, I really struggled with this aloneness and had a strong desire to come out to my friends and family. I will share my experience with coming out to others at the end of this post, but for now, let’s focus on the pros and cons of coming out to friends and family about Lichen Sclerosus.
Why You Might Want to Come Out to Others: The Pros
Why You Might Not Want to Come out to Others: The Cons
Tips and Tricks for Coming Out to Others
What follows are some tips and tricks I have with respect to coming out to friends and family (if this is something you would like to do but have no idea where to begin).
The Early Stage of Coming Out
The Later Stage of Coming Out
So you know the why behind telling others about your Lichen Sclerosus and you’re getting close to confiding in someone; here are some more tips on how to proceed.
The Conversation
So your family or friend says they have the time and space for you and do not mind at all if you discuss your vulva – what’s next? Let’s talk about the actual conversation.
My Experience Coming Out to Others
I’m fortunate that everyone I came out to was incredibly warm and supportive. When I was diagnosed, I didn’t know anyone with LS, and, consequently, I had no one to confide in. Thus, I felt even more compelled to tell others because I knew bottling it in wouldn’t be good for my mental health. The day I was diagnosed, I called my stepmom, my dad, and my sister. Later when my husband came home from work, I told him. Everyone was incredibly understanding and compassionate. I was a blubbering mess when I told them, but nonetheless, they met me where I was at and offered me tons of support and love.
After this, I messaged some of my close friends. I asked them if they had time and space for a conversation, and I warned them I’d probably cry and that it was about my vulva. I was quite nervous, but they honestly blew my mind with their level of compassion. They were so warm, caring, and reassuring. They assured me they would still stay with/date someone with Lichen Sclerosus, and that my vulva was beautiful even if I was super small down there and lost my labia. This honestly really helped up my confidence.
And now, everyone and their neighbor know I have Lichen Sclerosus and I’m happy about this. It makes my relationships and interactions with others so much easier. For example, once I was at a friend's house getting ready for a wedding. I pulled the owner aside, explained I had LS and that I was flaring and if I could step away from the festivities and soak in the tub and apply my steroid.
She said absolutely, set me up in her bathtub, and said if I needed anything else to let her know. I was able to enjoy the rest of the day because of this instead of toughing it out and suffering in silence. For me, it feels liberating and empowering to tell others about my Lichen Sclerosus.
Conclusion
To conclude, there are a number of reasons why you might want to come out to friends and family. For example, it can help build stronger relationships, create a stronger and more diverse support system, and provide context to your actions. In this post, I shared my tips and tricks to make coming out to friends easier. Be sure to bookmark this page to come back to it when you are ready to tell others about your LS.
#TLLCTuesdayTip: Practice self-care after you tell someone about your Lichen Sclerosus. This is very vulnerable and can bring up a lot of emotions.
Send me an email by filling out my contact form here or send me a DM on Instagram, TikTok, or Facebook (@thelostlabiachronicles).
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*The Lost Labia Chronicles does not provide medical advice or engage in the practice of medicine. The information provided by The Lost Labia Chronicles is for education and entertainment purposes only and does not under any circumstances constitute medical advice. Please consult with your healthcare provider before making any changes to your healthcare plan.
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