--> My Reality of Living as a BDSM Slave 24/7 While Dealing with Epilepsy | BDSM Unveiled

I always get emails asking how can I possibly live as a BDSM slave 24/7. I also get told that it's impossible to do it in today's world. I get others questioning like how do I balance being a slave while dealing with my epilepsy. Along this same line of questioning, I get the naysayers saying it's not possible because my illness takes up too much time.

Living as BDSM slave dealing with Epilepsy Reality

I do live as a very proud BDSM slave every single day of the week, month, and year. It's very possible and I've proven over the past 4 1/2 years it's very doable.  Of course, it takes constant work from both Padrone and myself but we want this type of relationship and we make it work. 

How do we balance 'normal life stuff' with our M/s dynamic? Simple. We each know our roles. His is Master and mine is as his slave. I always do things that make his life, and in reality both of our lives, run smoother and easier. I never do anything to hurt or antagonize him. He guides me and I listen. Sometimes I am a little hard headed but in the end, I always listen. We always tell the other everything, no matter if it is good, bad or ugly. We try to never use hurtful words to the other. We've learned to never raise our voices during a very rare disagreement.  

No matter what I'm doing, if he calls for me or asks something of me, I stop whatever I was doing and proceed to do what was asked with no complaints or grumbling. Why? Because that's the way a slave behaves and it makes me happy to do it. Every dynamic might not work like this, but ours does. I have no doubts about anything when it comes to Padrone. No reservations or hesitations. That's the kind of trust every slave should have with their Master. I know he would never use me in a way to hurt me or lead me down the wrong path. He always puts my welfare first. 

I have had so many problems with my epilepsy these past few weeks and have been unable to do many of my normal duties but I still do whatever I can. During my down times, Padrone is right there supporting me, helping me in whatever way he can, and just being there for me. He cooks, feeds me, helps me walk when needed, applies medicine to my back, gives me massages, and whatever else he thinks will help. Some people would see this as not being the role of a Master. To me, he is a perfect example of what every Dominant that calls themselves Master should be. He is not switching and taking on the role of sub or slave. He is taking care of his slave, his property, the one he values more than anyone else in the world. Me. 

Is it difficult to deal with epilepsy, especially the weird and ever evolving kind that I have? Yes. It's difficult to just try to live what most people consider a normal life. I have many duties that I consider part of my submissive tasks. Padrone has never assigned any specific tasks to me, I just knew what to do and do them. With the physical manifestations my epilepsy has forced me to deal with this past week, many of these duties have not been accomplished because I am just not able. 

While I feel extremely frustrated, weak, and somewhat of a failure, Padrone never once said that. He constantly tells me how wonderful I am, how brave and beautiful I am to be dealing with so much pain and limitations. He keeps giving me encouraging words that come from his heart because he knows they help take my feeling of failure as a submissive away. 

Being a slave doesn't mean I'm constantly bowing, kneeling, having sex, performing some type of bondage scene, being lead around on a leash, or cleaning the entire house with a toothbrush. That might be someone's reality, but that is not mine. Being a slave, the way we practice an M/s relationship, is anticipating every need Padrone may have. Cooking and cleaning to make him happy and comfortable. Staying by his side so that he sleeps better knowing I'm there. Snuggling and watching TV. Joking, laughing, loving, and living. It encompasses every part of our lives. 

Being his slave means that yes, I am his property. I am his to use and do with as he pleases, anytime he wishes. But I am not a doormat or a quiet mouse. I have my own personality, thoughts and feelings. He has his own way of doing things, feelings and thoughts. But, we are one of the lucky couples that compliment each other perfectly. Our beliefs are the same, our likes, dislikes, and morals are all very similar. He is the perfect dominant to my submissive. 

In good and bad health, no matter what the problem may be, we are always together, supporting and loving each other as best we can. Living with a chronic illness is not fun, but it does not stop me from being a slave 24/7. It may slow down certain activities, but I always do my best and I am always Padrone's slave. 

I encourage those of you that have a chronic illness to not let it get you down and discouraged. Deal with it the best you can. Stay positive and focused, and most of all never give up. You can live a full life and have the type of BDSM relationship you want even while dealing with health problems. You just need to find the perfect fit for you. Or, as Padrone says in his Italian accented English, "Find your purrfect feet!"




Post title: " My Reality of Living as a BDSM Slave 24/7 While Dealing with Epilepsy "
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3 comments :

  1. You are an amazing couple, truly. I live with migraines and back and knee pain 24/7 that most of the time is cripling especially when the weather changes cold to hot or hot to cold. Sun and flouscent lights are a trigger to my migraines so needless to say I don't get out much. Living the lifestyle is only a dream for me. I went to a much and a few outting locally a few evenings when I wwas able and was pretty much shunned so I just gave um on that idea. I am resigned to live my life as I alway have safe and sound with my dogs and my daughter helping take care of me when needed. I apploud you both for being an insperation to the community.
    Dawn

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  2. Thank You so much for writing this! I have a Chronic Illness, Lupus and Fibromyalgia. I sometimes find it hard to deal with and I am in that phase now and needed to read this post. Again thank you for writing it, I definitely needed to see those encouraging words today.

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  3. Like you, I'm epileptic. I also have a multitude of other illnesses with it (Chiari 1, Syringomyelia, Fibromyalgia, PCOS, and asthma).
    I agree with everything you say. I do anything and everything I can for Sir. When he speaks I listen, he asks, I do, etc. It just is, that way. Then when I am poorly, he takes care of me. I have night seizures, most nights, and he always gets up early and looks after the kids. He does this because he loves me and I'm his. :-)

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