March is National Endometriosis Month

March is National Endometriosis Month

Endometriosis is incredibly painful. I don’t live with it but have friends who do and the pain they experience is hard to even witness third-person.

What is it?

Endo is a condition where the material that lines the inside of the uterus (endometrium) begins to grow outside the uterus. Usually, it seems to stay on the uterus, but it can affect other organs as well. This can create cysts, lesions, and scar tissue that has to be removed.

Pain increases with menstruation, bathrooming, and sexual activity.

Fertility is affected as well. Eggs may not be able to be released from the ovaries, may not be able to travel down the fallopian tubes, and may not be able to attach themselves to the uterine wall.

Treatments that address pain control, hormone therapy such as birth control pills, surgery, and hysterectomy may all be needed.

Where can I learn more?

ask me about my uterus

If you’d like to learn more about what endo feels like, please check out my pal Abby Norman. She has been featured by Glamour Magazine, Huffington Post, Seventeen, Forbes, The Atlantic, Bustle, and more. and has presented at conferences such at MedX and the Endometriosis Foundation of America Medical Conference.

In addition to being an excellent writer, she runs Ask Me About My Uterus. AMAMU discusses issues related to endo, miscarriage, birth control, menopause, pregnancy, menstruation, and more.

The Endometriosis Foundation of America is another great resource.

HEART Women & Girls: Launchgood Campaign

HEART Women & Girls is one of my favorite organizations. They are a Muslim-led organization that focuses on promoting sexual health, personal agency, equality, and awareness of sexual violence. By ending the silence of all these issues, we can help to end problems.

They are currently working to raise money in order to grow their virtual library. These beautiful resources are great for everyone, no matter your religious or spiritual background. Check out their birth control FAQs video below:

It’s so important, especially now, for us to support the Muslim community in these endeavors. HEART is a great organization with amazing resources that are so useful to so many. I, for one, am excited to see what amazing resources they come up with next.

What’s on the docket? Videos on anatomy, menstruation, talking to doctors about reproductive/sexual things, pap smears, and more!

Would you like to help donate? Visit HEART’s campaign on Launchgood.

 

review: calice from fun factory

Review: Calice from Fun Factory

Disclosure: As a Fun Factory affiliate, I receive sex toys each month in exchange for my honest review of them. This system in no way affects my opinions of these products. This review has affiliate links.

Today, I’ll be reviewing the Calice :

First, let’s check some facts.

The Calice is made of silicone, so don’t use silicone or oily lubes as they can degrade the toy/change the consistency of the material. It’s also totally waterproof which I love. It charges through a USB cord that connects magnetically to the bottom of the device.

For those interested in stats, the Calice is 6.5 inches long and 1.4 inches in diameter. There are also six different vibration types along with six different intensities.

I’ll be real – I chose this vibrator because of the unique shape it has. It’s enough like a dildo, the top like the head of a penis. Still, the interesting shape at the top and front was intriguing. It actually made it very easy to add lube as I was able to slide the lube down the notch in the shaft.

When I opened this up, I really was most excited for the cut-out at the top. I hope that it would make this a great tool for clitoris stimulation – and I wasn’t let down. That made it great not only for targeting the clit, but the nipples and even for edging (if you haven’t tried edging, I certainly highly suggest it). The dildo-like shape, combined with the soft material, really made this an exciting toy to use, too.

I honestly became turned on just by thinking about using this toy after the first use. It’s the first sex toy I’ve gotten turned on by before using! Since I have some arousal issues, that’s saying a lot, too!

As a vagina-haver, I’m unsure how this would work for penis-havers, but this seems like a toy that would very easily stimulate the prostate from the outside via the perineum/taint. The lack of a flared base means anal play is a little risky with this toy. I certainly wouldn’t recommend it for anal play on your own, but it could potentially be okay with a partner.

calice buttons

Because of my systemic juvenile arthritis, my hands don’t always work well – especially in awkward positions like using a vibrator. I love the shape of this vibrator, though. It’s easy to hold and the buttons to change vibration and intensity are accessible while using this toy. The buttons aren’t in the way enough where I accidentally changed anything I didn’t mean to, either, which is nice.

The power is great, even on some rough fibromyalgia days. For those unfamiliar, fibro can make common sensations – even clothing – hurt. When I’m having a fibro day, I can’t be touched, wear clothing, or even have contact with rougher surfaces. Since the Calice is so soft – and easy to control with regards to sensation and intensity – it’s the only vibrator I’ve been able to use during a fibro day that didn’t cause more pain.

All in all, this toy was incredibly accessible for me. The Fun Factory lubricant combined with the toy’s effectiveness, unique shape, easy button-based controls, and power really have turned me on to more vibrators. I highly suggest it for those who enjoy dildos, vibrators, and uniquely shaped sex toys.

You can shop the general Fun Factory site using my affiliate link or go right to the Calice. Shopping using these two affiliate links is a great way to support Chronic Sex in addition to getting yourself something fun.

A Directory of Sex and Disability Speakers

I wish this wasn’t a conversation we had to have in 2017 but, alas, it is.

Many conferences and talks centering on disability don’t include those of us with disabilities. This is especially true when it comes to sex and intimacy centered spaces.

One of the most difficult parts of being a part of a marginalized group like having a chronic illness/pain condition/disability is that we are so often talked *about* without being included in on these conversations. This violates the basic ‘Nothing about us without us’ mantra that so many activists in the disability/illness/pain realm live by. It also serves to eliminate intersectionality when it comes to our experiences.

One barrier to our involvement in conferences and events is that there isn’t always a lot of press around the work we do; additionally, there isn’t one single place people can go to find us.

My pal Kate McCombs and I are aiming to change that. We are creating a directory of people with disabilities who speak on sex, sexuality, and other intimacy-related topics. You can check out those who have already added their names here. If you’d like to add your name, please fill out our Google Form.

Episode 9: Lene

This week, I talk with photographer, writer/author, and general badass: Lene Andersen. As you will hear, she is one of the reasons that Chronic Sex started. She is a wonderful advocate, activist, and pal. Keep in mind that this episode was recorded over the summer of 2016. That said, we mention a contest for SYLK that has since run and ended.

You can find links for Lene below:

We mention the following:

Visit us on SoundCloud, iTunes, or your favorite streaming app. While you’re listening, make sure to subscribe, rate, or comment on the Chronic Sex Podcast using whichever app you stream through. The more you do this, the more other people see this work.

As always, please support this work if you can. You can donate monthly on Patreon, give a one-time donation on iFundWomen, or visit the ‘support us‘ page above for other ideas. You can also volunteer to transcribe podcast episodes or a number of other things.

A quick note: Normally, Thursday evenings are our chat nights as well. I’m battling some migraine-related issues and unfortunately don’t have enough brain power to run chat tonight. Join us next week for chat – and in two weeks for a new podcast episode.

Featured on Andrew Gurza’s Disability After Dark Podcast

I am so beyond excited to share Andrew’s work. He is my cripple from another nipple and we’re practically in work-love.

Andrew runs two podcasts. Disability with Drew covers disability culture and really what types of things those of us who identify as disabled face on a day-to-day basis. Disability After Dark is all about

Andrew recently had me on Disability After Dark – come check out the episode here or on your favorite podcast streaming app.

Make sure to check out past episodes because both of these podcasts are amazing. You can also pop over to Patreon to support Andrew’s work.

Episode 8: Niko

Today is the Day Without Immigrants and, as such, it’s time to hear from an amazing immigrant – my friend, Niko. Originally from Trinidad & Tobago, Niko is an undocumented immigrant. We talk mostly about myths regarding undocumented people, politics, and empathy. We also touch on the difficulties of living with chronic illnesses.

Take a listen on SoundCloudiTunes, or your favorite podcast app.

Niko and I talk a lot about empathy. Below are some great resources for empathy work:

Please remember that I’m looking for volunteers for transcriptions.

As a note: our chats are now Thursdays at 8 pm Eastern (New York City) Time | 7 pm Central (Chicago) | 6 pm Mountain (Denver) | 5 pm Pacific (Los Angeles) | 4 pm Alaska | 3 pm Hawaii. A new time will be coming soon earlier in the day for those who cannot make it during the above times.

Chronic Illness & Intimate Relationships – An Interview with Dr. Logan Levkoff

This piece comes from one of my favorite people, Mariah Leach of From This Point. Forward. Mariah is one of my favorite people and, indeed, one of my favorite partners in crime.

For the past few years, I’ve been writing openly about the impact of chronic illness on intimacy and relationships – so I was excited when I was recently offered the opportunity to interview Dr. Logan Levkoff. A recognized expert on sexuality and relationships, you may have seen Logan on the reality show Married at First Sight. Logan is dedicated to perpetuating healthy and positive messages about sexuality and relationships, and she recognizes the added struggles a chronic illness can bring to the table.

Mariah: If one partner has a chronic illness, what can a couple do to try to address the diagnosis as a team? What if your partner is having a difficult time understanding or accepting the impact of your diagnosis?

Logan: I think it’s sort of funny – we share our bodies with our partner, but that doesn’t mean we feel able to easily talk about the feelings that go with that experience. None of these conversations are easy – they don’t come naturally – but we have to have them. “Communication” as an answer to this question is not the most novel idea, but there’s really no other way to do it. Your partner doesn’t understand what you are experiencing and vice versa, so we have to find ways to explain what we are experiencing. Listening is important too, as is considering your partner’s needs. Try turning the question around and asking your partner what they are experiencing, without making any assumptions.

Mariah: I think it can often be really difficult to consider your partner’s needs and experiences when you are really hurting or suffering yourself. What do you recommend if you are struggling to make room for your partner’s perspective?

Logan: It’s definitely a delicate balance between explaining your own needs and listening to your partner’s needs. If you mess up and end up in an argument instead of a conversation, you can always go back after the fact and say to your partner “I really wasn’t feeling well when we had that conversation, but that doesn’t mean what you are thinking is not important.” If you really struggle in this area, it may also be useful to have a third party, such as your healthcare provider, offer some information to your partner about how your chronic illness may impact intimacy. For example, after a woman gives birth their partner may not understand why they can’t be sexual, and a doctor can help explain the issue. A third party can also moderate the discussion, give information, and give your partner some idea of what to expect.

Mariah: That’s a good suggestion, but to get that sort of help from your doctor you have to bring up the issue in the first place. Do you have any advice for making it easier to talk to your doctor about this sensitive topic?

Logan: It really depends on the relationship you have with your doctor. If you’re uncomfortable, sometimes it can be easier to call the office in advance, tell them you’d like to talk about X subject, and ask them to make a note in the file to reserve the time during your next appointment. When you go in for your appointment, it may also help to have a list of questions. Even if you don’t really need a list it can serve as a psychological crutch to look down and read something off a piece of paper, instead of asking directly.

And you can always lead off with “I don’t know how to say this, but I need some guidance.” Nurses and nurse practitioners can be a good starting point too.

Mariah: So once you’ve gotten some advice from your doctor and figured out how to communicate better with your partner, what if you just don’t feel sexy? How can you learn to love your body in the face of chronic pain or in spite of the negative side effects from treatments?

Logan: We all have moments when we don’t feel our best, and it’s often because we have this idea that someone else sees us in a different way. There are times when we don’t give ourselves enough freedom to think about what really makes us feel good – sexy, fulfilled – beyond the role of being someone’s partner. As a starting place, ask yourself the question “when do I feel my best? What puts me in a space that I can let some of my worries go.”

Mariah: Do you have any advice on dealing with guilt over the impact your disease has on your partner’s life?

Logan: We often feel guilt because we feel like we are depriving our partner of something – and we tend to assume that we know how our partner is feeling about the issue. It’s about saying to your partner “I really want for us to have the most fulfilling intimate life possible. I’m sorry there are times we can’t get there – but what can we do together so we feel connected even when I’m not able to be physical with you?” We often avoid these types of conversations because it feels safer, but being vulnerable and owning it shows your partner that the issue is important to you. It may not be the exact journey you expected to be on, but it can still be fulfilling.

Mariah: What advice might you give to the “healthy” partner in a relationship facing chronic illness?

Logan: Honestly, I think these general thoughts apply to everyone. We often have this fairy tale idea of how relationships are supposed to look, act, evolve, etc. Get rid of that. Chronic illness or not, no one lives that life. Expectations don’t serve our purposes – for anyone. I’d also encourage the “healthy” partner to acknowledge that the situation may not be what they imagined, but that just means we have to change our definition of what fulfilling means. There are plenty of intimate things you can do to feel fulfilled – it doesn’t always have to be intercourse. Numbers and statistics and measuring seems to count, like we may see on the cover of a magazine, but the reality is that life isn’t supposed to be like that. The “healthy” partner could start by saying something like, “tell me how your pain makes you feel so I can understand where you are coming from and help you manage that.”

Mariah: Finding different ways to maintain intimacy despite pain is super important, but it can also be a challenge. Can you recommend any toys or props you think would be particularly useful for maintaining a healthy sex life while living with chronic pain?

Logan: I like to say “enhancements” rather than “toys or props,” because we are looking for something to help enhance the experience, not to replace any part of it. My advice would be less about particular products and more about things to look for. Realistically, texture can be an issue of you have sensitivity, so it may help to consider the size and weight, shape, and range of speed and pressure. Also volume, especially if you have small people in the house! Online research can be helpful – there are sites that have great reviews and people you can chat with. Or, if you have the ability, you can visit a store and feel the products yourself and ask questions. Keep in mind that what is good for one person isn’t necessarily good for another.

Mariah: Speaking of small people in the house, what advice do you have for women trying to balance chronic illness and an intimate relationship and motherhood?

Logan: Don’t expect it to be perfect and graceful all the time. Women can have and do it all – with the caveat being that we won’t do it all perfectly all of the time. It’s ok to admit that you have limitations – that doesn’t mean you don’t love your kids or partner. But you end up hurting yourself and feeling overextended if you don’t recognize your own limitations. Primary caregivers for small people also end up being touched and groped all day long, and when a partner comes home and touches you the brain doesn’t necessarily read it the way the touch was intended – it may seem like one more hand that wants something. But your partner, who may have had no physical affection all day, may see it as a rejection. We need to say “I love you, but I need you to know my brain is reading this as a demand.” This comes back to the importance of communicating our experiences to each other.

Mariah: Communication is certainly key to having a healthy intimate relationship despite chronic illness. I think you’re right that it’s important to remember that those conversations may not be easy – but they are necessary. Thanks so much for taking the time to chat about this subject!

You can find Dr. Logan Levkoff on Twitter, Facebook, Instagram, Huffington Post, and on her website. She is also partnering with Pfizer to talk about the emotional effects of living with arthritis – like how it affects sex and relationships! Visit Arthritis.com to learn more.