Questions about H? Register for our live streaming call this Thursday night. I’ll answer the questions you’re afraid to ask your doctor.
You Can Register HERE: https://pinktent.com/event/dessert-discussion-10-4-18/
Questions about H? Register for our live streaming call this Thursday night. I’ll answer the questions you’re afraid to ask your doctor.
You Can Register HERE: https://pinktent.com/event/dessert-discussion-10-4-18/
Why do so many women give their power and self-confidence away to Facebook?
What used to be a fun place to connect and share, has now become a place that leaves so many women feeling depressed, isolated, exhausted, jealous, ugly, anxious and powerless.
Single Women, Moms, Female Doctors, Teenage Girls, Successful women, Millionaires, Teachers, Fitness Instructors …you name it…women of all sorts of backgrounds are ruining their self esteem and self worth through Facebook.
Unfortunately, the same platform that can leave women jumping for joy and inspired to live a great life, so often it does just the opposite. They walk away from our computers feeling like CRAP!
So…why are some women’s feelings of self-worth and self-esteem so dependent on the likes and shares they receive?
Research has shown that…
People who are more goal oriented and feel a sense of purpose in life are less sensitive to their Facebook or social media’s responses.
Why? Because people who are more goal oriented are more likely to think of their empowering future and what lies ahead. They don’t need the quick fix of a like to prove that they are progressing towards their dreams. If you have a dream and a plan and you are taking action towards that plan…you are able to see into your future.
People who lack goals often suffer from the need to get their emotional needs met in the short term vs long term. They want success now and they are unwilling to pay their dues for love, health, money, a dream home, dream career etc. So, when they see someone else on Facebook that has what they want… they become jealous, sad, and self-sabotaging.
When we have a sense of purpose, our life has meaning. We feel a deeper connection with people and the outside world. We know that we have something to contribute. So, if you know you have a purpose, you aren’t so bummed out when your Facebook posse doesn’t “like” your posts.
How to turn your Goddess Confidence ON
-Do a Facebook Detox for 30 days or more and see if your self-confidence increases
–Set some GOALS– short term and long term and start taking baby steps to achieve them
-Estimate how much time you spend on Facebook and redirect your focus and time to Self Love activities
-Turn Facebook Jealousy into a game plan to go out and get what you want!
-Challenge yourself: Come up with a list of 100 things you LOVE about yourself
Want to learn more?
Did you know that herpes symptoms in women can be confused with many common conditions? 85% of people with herpes don’t know they have it! Common symptoms include blisters, sores, itchy areas, tingling, burning, painful urination, skin fissures and cracks, skin ulcers, swollen lymph nodes, fatigue, depression, pain down the leg, flu like symptoms, body aches and watery vaginal discharge; but how do you know if it is herpes? I have worked with women who were misdiagnosed with several other ailments before they were ever PROPERLY diagnosed with herpes.
Why does this happen?
Herpes is truly the Great Masquerader. Doctors and patients alike misdiagnose herpes all the time. Here is a chart of what women with herpes think they have and what men with herpes think they have.
What Women With Herpes Think They Have | What Men With Herpes Think They Have |
Yeast Infection | Folliculitis |
Urinary Tract Infection | Jock Itch |
Menstrual Complaints | Normal Itch |
Hemorrhoids | Hemorrhoids |
Heat Rash | Zipper Burn |
Urethral Syndrome | Insect or Spider Bite |
Allergy to condoms, spermicides, sperm, elastic/pantyhose | Allergies to condoms |
Irritation from bike seat, shaving, douching | Irritation from bike seat, tight jeans, sexual intercourse |
It’s not that you don’t have enough Zoloft running through your veins, it’s just that you are believing your thoughts about what it means to have herpes.
Most of you are thinking that…
No one will ever love me OR
My symptoms will NEVER get under control OR
People are going to think of me differently.
While these are all common thoughts, they do not need to be your TRUTH.
The truth is that you CAN overcome these thoughts about this diagnosis and rediscover hope, healing, and happiness.
If you are tired of feeling depressed…here is what you need to do.
You need to get out of your head and back into your heart!
While you probably haven’t felt like doing the things you love to do and are passionate about….I’m here to kick your butt and tell you that it is time to return to your passions, even if it is just for 30 minutes.
Here is a quick video from me to you from the beautiful mountains of Colorado. I wanted to send it to you yesterday, but I guess it was meant to happen today.
You know why? I just found out that Warren Miller, a ski movie icon, at 93 years old died today. He created a whole industry and lifestyle around his number one passion, skiing. I was introduced to him and his ski movies at the age of 8. Here is a video that I dedicate to him. May you rediscover your passions and not give up on happiness!
Many anthropologists, sociologists, and feminist theorists have explored the reasoning behind women’s sexuality, or rather the reasoning for the almost absence of women’s sexuality in today’s society. Because women’s ability to have sexual desires based on their own personal desires, and not those of a man, is frequently discredited by mainstream society, women’s sexuality automatically becomes discredited as a whole. The idea that sexuality is socially constructed based on things we learn from media, religion, schools, and other great institutions is a common theory.
Scholars in this area have also taken specific interest in the way that an STD diagnosis might affect how a person experiences sexuality based on the social construction and meaning on the diagnosis.
Women’s sexuality is already invalidated, so an STD diagnosis simply invalidates it further based on her supposed deviation form the female sexual norm (having sexual desires, acting upon them, and being diagnosed with an STD because of those actions).
There are plenty of articles and scholarly works out there discussing this issue from an outside perspective, but I would like to share my personal experience of dealing with my new sexual identity after being diagnosed with herpes. I would like to emphasize that my perspective is very heterosexual, for lack of a better term, but I believe there will be plenty of parallels for those who identify elsewhere on the spectrum.
As I feel many young women believe when they first begin to experience their sexual selves, my sexuality was based solely on what I thought my male partner wanted.
Neither the media, school, nor my parents had ever taught me what sex or intimacy should be from a woman’s perspective. It was always based on heterosexual male pleasure.
That being the case, when I learned I had herpes I felt I could no longer fulfill those sexual desires for someone else again because I was no longer desirable to men based on my new label as a “sexual deviant.”
I would like to break down my experience into stages that coincide with Dr. Kelly’s “Stages of Grief” in her book Live, Love, & Thrive with Herpes in hopes that many of you can connect to one, a few, or maybe even all of them as you begin to find sexual freedom after your diagnosis.
Stages to Sexual Freedom:
Avoidance (Trauma and Denial/Feelings of Rage)
When I was first diagnosed I had an irrational fear of spreading herpes to anyone I had any sexual contact with at all. I say irrational, because as I learned more about the transmission of the virus, I discovered there are plenty of ways to reduce the likelihood of transmission as well as ways avoid the possibility of transmission completely.
Because of my fear, during this stage I completely avoided any situation that could lead to sexual desire, including dating.
Trauma and Denial, as Dr. Kelly emphasizes in her book, played a huge role in my avoidance. The trauma of my diagnosis as well as my denial made disclosure impossible at the time. I was not ready to disclose my situation with someone, and I knew I had to do so before becoming intimate again.
Settling (Profound and Prolonged Sadness)
Looking back on my journey, this stage brings me the most sadness, which directly relates to Dr. Kelly’s explanation of Stage Three in her book.
During the “Settling” stage my mind set was to “take what I can get.” If a man said he loved me or that he found me irresistible despite my herpes I thought I had to reciprocate those feelings. This is because I thought it was so incredibly rare for a man to feel these things about me after my diagnosis that it might be my only chance to find love or intimacy again.
After going through this stage, my blunt advice is that this is NOT TRUE. There will be many men or women that love you and find you undoubtedly sexy not despite your herpes, but almost by virtue of your herpes and the woman it has created.
Fear of Control (Communicating and Reaching Out)
This stage was by far the longest of the four because it took me so long time to understand my thought process during it.
As women we already sometimes feel a lack of control with our sexuality and sexual decisions based on the submissiveness we learn from society. After I began to seek intimacy again after settling for men I did not necessarily desire, I found it… but on someone else’s terms.
I believed that I no longer had the right to share my opinions about what I desired sexually because it was unfair to ask someone to put himself at risk for my pleasure. What I learned after verbally expressing my thoughts to loved ones was that I have just as much control over how I experience sex and intimacy as I did before.
I was afraid to take control of my sexuality again because that could mean putting someone else at risk. What I didn’t realize is that if I had disclosed my diagnosis and shared the transmission risks with my partner I had done my part in keeping him safe.
This is where Dr. Kelly’s stage on communicating and reaching out becomes so important. Without my ability to do so, I may not have allowed control back into my intimate experiences.
Freedom (Surrender and Acceptance/Empowerment)
After effectively communicating and finding the ability to reach out and seek advice from friends and family, I am finally able to enjoy my sexuality and be at peace with my diagnosis.
I have accepted that I cannot have spontaneous sexual encounters without putting others at risk, and I now understand how that is not at all a curse; it is actually a true blessing.
I have accepted that I need to be at a more intimate level with someone before I share my sexuality with them in order to feel comfortable and in control of the situation. Once again, this has proved to be a huge blessing in my life.
Finally, I have accepted that my herpes diagnosis has not hindered or tainted my sexuality in any way, but rather it has forced me to embrace every piece of my self in order to find true intimacy with another person.
I encourage you all, as I always do, to find the silver lining in situations where you feel that your herpes might have given you the short end of the stick. I can guarantee that once you start searching, you will find all the amazing ways that herpes has allowed you to grow as a woman in every way, including your sexual being.
MPWH: The New Herpes Dating App
By Contributing Author: Stephanie
Have you heard the news? Apparently there is a new herpes dating app that works somewhat like tinder. I would like to use this blog to start the discussion on what apps like this mean for our community.
As I’m sure many of you are aware of, online dating and dating apps have become increasingly popular over the last decade. Different sites like Positive Singles and Herpes Singles are designed specifically for people seeking the online dating experience who have been diagnosed with herpes or other chronic STDs. The new app, MPWH, stands for Meeting People with Herpes. Although this runs as a website, there is also an app free for downloading on iOS and Android systems. I have never used online dating apps, or herpes specific dating apps, but I have given the concept a lot of thought. I am going to lay out the pros and cons of using herpes dating apps and websites to the best of my ability, but I would like to hear from you all about your own experience with the world of online dating with herpes!
Pros:
I personally believe that the herpes dating websites have a lot to offer, especially for newly diagnosed individuals. In my experience, it was extremely scary to start dating again after my diagnosis. I was constantly worried about how and when I would have “the talk.” For some reason rejection got a lot harder when it had to do with my sexual health status. Being able to date without worrying about “the talk” would have made the traumatic shift in the perception of my love life a bit easier.
I also think that an app like MPWH could be beneficial just for the sake of what I will call sexual sanity. Just because we have been diagnosed with an STD does not mean that we do not have the right to enjoy casual sex if that is what we desire. These websites could be a great place to meet someone to have a casual dating relationship with, without having to worry about transmitting the virus. So long as the person you meet has the same type of HSV as you, and they do not have any other STDs, these websites give you access to have freedom and safety in casual sex.
One last pro is the way that these apps and websites show the prevalence of genital herpes in the world. A herpes diagnosis can make us feel completely alone and unwanted if we allow the virus to make us feel like a victim. These websites show the surprising amount of people who are living with the same virus as us, and that can be extremely comforting in times of loneliness!
Cons:
The first con that came to mind when I began to think critically about these websites and apps is the possibility of transmitting different types of the herpes virus back and forth, or even contracting another STD. Many sites are herpes specific, but sites like Positive Single target anyone with any STD. I urge you all to be smart when using these apps and websites for the sake of your own health and other’s health.
Although I agree that dating within the herpes community can be a great start to getting back out there after a diagnosis, I also argue that this can be limiting to a person’s dating life. Sometimes I wonder if only dating other people with herpes can hold us back from seeing our true potential as an intimate partner. It is inevitable that some people will not be accepting of our diagnosis, but it is also inevitable that some people will! I think it is great to challenge ourselves to move outside of the herpes community to find love and support. I think you will surprised with what you find!
Now I would like to hear thoughts and opinions from you all on the pros and cons of: 1) herpes dating websites and apps, and 2) only dating within the herpes community. Feel free to ask me, Dr. Kelly, and each other questions. I am looking forward to hearing about all the different experiences each of you have had!
About Stephanie
Hi Everyone! My name is Stephanie. I was diagnosed with HSV-2 in April of 2014 when I was 22 years old. Right now, almost three years later, I am a doctoral student in the sociology department at Purdue University. I recently completed my MA in sociology at the University of Northern Colorado where I explored the role of stigma in the process of disclosing a genital herpes diagnosis. With that said, if anyone is interested in reading what I discovered in my project, I am happy to share that with you! I plan to continue advocating for our community, as well as studying the social factors that influence sexual health in order to understand how we can create a world that is easier for people diagnosed with STIs. I really enjoy writing for the Pink Tent community and am excited to be able to share some of my experiences and thoughts about living with genital herpes with you all.
As I was beginning to write this blog, I started with looking for articles about self-love. There are so many articles out there telling us how to love ourselves and how to practice as much patience with ourselves as we do with others. Although these are all beautiful and inspiring articles I found that the majority was missing one thing. What do we do when we feel completely unable to love the person we are today, right at this moment?
This is something I have struggled with my whole life, but when I was diagnosed with herpes it became even more difficult. As women we are constantly surrounded by messages and images telling us what beautiful is, what the ideal woman acts like, and what our health says about our character as women. It can be extremely difficult to push those messages aside in order to learn to really love yourself, but I would like to share with you all how I have been able to start to do just that in order to accept myself exactly the way that I am. Over the last year I have made it a priority to really get to know myself. By that I mean I wanted to know what makes me feel happy, sad, excited, anxious, and what things were really most important to me in my life. Through my efforts this year I have been able to understand what triggers my emotions, what I really value in my life, and many other things I would have never guessed were a part of who I am a year ago.
Interestingly enough, understanding myself in these ways has helped me to fall in love with the person that I am. When reflecting on this experience, I like to compare it to falling in love with another person. As we get to know someone, either intimately or as a friend, we start to accept that person for everything he or she is as well as everything he or she is not. As we accept a person for all he or she has to offer we can start to really love that person unconditionally. I believe this is what has happened in my relationship with myself over the last year. By allowing myself to get to know me I have been able to accept myself for everything that I am, and that has given me the ability to love myself unconditionally, herpes and all. I challenge you all to get to know yourselves on the same intimate level you might imagine you would get to know your life partner on.
If you are struggling with accepting yourself as a woman diagnosed with herpes, understanding deeper traits about yourself will allow you to put less emphasis on such a small aspect of your health and life. Remember that others will only judge you as much as you judge yourself. I hope what I have discovered will help you all as you begin the same journey that I started a year ago. Be your biggest fan, and the journey towards unconditional self-love will be easy.
By Contributing Author Stephanie
I watched this video quite a few months ago and for a long time did not understand my connection to Eleanor Longden or her struggle with mental health. After much contemplation I began to understand my ability to empathize with her and be overwhelmingly inspired by her journey. Although her experience with schizophrenia is vastly different than my own experience with herpes, the fact of the matter is we both had to overcome societal stigma and as well personal stigma against our conditions.
To me, the most inspirational part of Eleanor’s story is her ability to not only overcome that stigma but to do so in a way that defied the norms of medicine and treatment for her condition. By overcoming the stigma associated with schizophrenia she was able to work with her symptoms and hardships in order to create a meaningful interaction with her voices. What she teaches any of us going through the process of overcoming stigma to promote healing is that doing so will allow you to experience your stigmatized identity in a way that is actually beneficial. For those of us dealing with a new herpes diagnosis, or the trauma that comes along with an outbreak after years of living with the virus, it is important to interact with our condition and symptoms in a compassionate way. My ability, and i’m sure many of yours, to understand Eleanor’s hardships is a perfect example of one way herpes has been beneficial in my life. Being able to feel true compassion and empathize for others in seemingly completely different situations than your own is a true gift that I may not have today without my diagnosis.
I hope you all find as much inspiration in Eleanor’s story and her ability to overcome stigma associated with her voices as I have; and I hope it inspires you all to find your unique path to health and happiness in your acceptance of your diagnosis.
About Stephanie
Hi Everyone! My name is Stephanie. I was diagnosed with HSV-2 in April of 2014 when I was 22 years old. Right now, almost three years later, I am a doctoral student in the sociology department at Purdue University. I recently completed my MA in sociology at the University of Northern Colorado where I explored the role of stigma in the process of disclosing a genital herpes diagnosis. With that said, if anyone is interested in reading what I discovered in my project, I am happy to share that with you! I plan to continue advocating for our community, as well as studying the social factors that influence sexual health in order to understand how we can create a world that is easier for people diagnosed with STIs. I really enjoy writing for the Pink Tent community and am excited to be able to share some of my experiences and thoughts about living with genital herpes with you all.
Prepare for Cold Season and Avoid Herpes Outbreaks
By Contributing Author Stephanie
As we enter into the beautiful, yet dangerously contagious, fall season I usually have one thing on my mind: avoiding colds. After being diagnosed with herpes, this concern weighs on my mind even more. As most of us know, the herpes virus shows up when our immune system has been compromised. There can be many causes for this including stress, another virus like the common cold or the flu, or perhaps even lack of sleep.
As my body was still trying to build up immunity to the herpes virus, colds had a substantial effect on my experience with outbreaks. For the first year of my diagnosis, every time I caught a small cold, an outbreak would follow days after the cold arrived. Because of this, I have found that it is extremely important for me to take care of myself and keep my immune system strong in order to avoid herpes outbreaks. This blog post will go over some simple, yet key points on how to boost your immune system during the cold season in order to avoid herpes outbreaks. The first step you can take to avoid herpes outbreaks by boosting your immune system is take Omega-3s on a daily basis.
In Dr. Kelly’s book, Live, Love, & Thrive with Herpes, she suggests 2000 mg or more a day. Omega-3s are a great way to boost your immune system as well as balance your hormones, and support cardiovascular and brain health. Zinc Chelate is another easy supplement to use to boost your immunity. Dr. Kelly’s book suggests 50 mg a day. Not only will taking Zinc on a daily basis support a strong immune system, but it will also promote skin health and tissue repair: two benefits that are amazing for herpes outbreaks. Vitamin D3 is also a great supplement to build immunity. The suggested dose listed in Dr. Kelly’s book is 5000 IU’s a day.
Women are often deficient in Vitamin D3 and new research is showing that it acts as a hormone, signaling cells to boost immunity. If you are osteoporotic, then D3 is required for you to be able to properly absorb your calcium supplements. Probiotics are another supplement to add to your regimen or diet, not only during cold season, but all the time. Probiotics help the “good bacteria” in your body to thrive so that they can fight off the “bad bacteria.” You may be able to get all the probiotics you need from your diet. A few of the foods known to be rich in probiotics are yogurt, sauerkraut, kefir, and kimchi.
One last supplement you should always take to support your health and immune system is a multivitamin. In Live, Love, & Thrive with Herpes, Dr. Kelly suggests a multivitamin that has at least 750 mg of calcium and 450 mg of magnesium. If you are already taking each of these supplements daily, congratulations! If you are not, now would be the perfect time to start. Cold season is among us, and supporting our immune systems is extremely important to avoid herpes outbreaks as well as for our overall health and happiness. I hope these suggestions find you well and that you all have a happy and healthy cold season.
By Contributing Author Stephanie
As many of you know from reading my short bio, I am working on earning my MA in Sociology. I was diagnosed with herpes right around the time that I was accepted into my program and made the decision to go to graduate school. As I was brainstorming ideas for my thesis, my own experience as a woman living with herpes sparked my topic. I am now in the midst of exploring the connection between social stigma and the disclosure process. I am determined to understand the role that stigma plays in the ability, or inability, to give “the talk.” I also want to know how the social stigma of herpes affects simple dynamics of “the talk.” By understanding the relationship between stigma and the disclosure process a bit more clearly, I hope to shed light on the way that stigma can affect transmission rates. If we can get people to feel more comfortable talking about their sexual health, there is a possibility that STD transmission rates could drop. Of course this assumption would need to be explored further than my own research in order to make this claim, but one thing we do know is that simply knowing you have an STD decreases the chance of passing it on to your partner.
Now that you have learned a little bit about my thesis and the agenda of it, I would like to invite any and all of you to be a part of the process. My methods for data collection include individual, qualitative interviews with people who have been diagnosed with genital herpes (type 1 or type 2) and wish to share their experience with me. The interviews will give you a chance to share your story, including triumphs and struggles with “the talk.” By talking with as many people in the herpes community as possible, I am hoping to paint a representative and accurate picture of the experience of living with herpes.
If you are interested in sharing your story with me, I would greatly appreciate your participation and ask that you contact me with any questions and concerns. The research is completely confidential, meaning there will be no names mentioned in the final report. I will be the only one with access to names of the participants, and measures like keeping files on a locked computer and using numeric identifiers and pseudonyms will be taken to protect your identity. If you wish to contact me about participating in the study you can reach me at: stephanienwilson@yahoo.com. I hope to hear from you all, and look forward to shedding light on the struggle associated with a genital herpes diagnosis through my thesis.
About Stephanie
Hi Everyone! My name is Stephanie. I was diagnosed with HSV-2 in April of 2014 when I was 22 years old. Right now, almost three years later, I am a doctoral student in the sociology department at Purdue University. I recently completed my MA in sociology at the University of Northern Colorado where I explored the role of stigma in the process of disclosing a genital herpes diagnosis. With that said, if anyone is interested in reading what I discovered in my project, I am happy to share that with you! I plan to continue advocating for our community, as well as studying the social factors that influence sexual health in order to understand how we can create a world that is easier for people diagnosed with STIs. I really enjoy writing for the Pink Tent community and am excited to be able to share some of my experiences and thoughts about living with genital herpes with you all.
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