As my physical therapy comes to an end, what’s next for me? I have a passion now to become an advocate
for women. I want to see women get the
help they deserve to live a life free of pain when having sex, to be able to use
tampons, etc. So, I started looking
online to see what I can find to get involved in.
Through my physical therapist’s website I ended up on the
International Pelvic Pain Society’s website.
On the front page was an article written by Amy Stein, a leader in
physical therapy for chronic pelvic pain sufferers and author of Heal Pelvic
Pain, regarding a Dr. Oz show that was done in 2010 on vaginismus. Amy is the founder and a practitioner of Beyond Basics Physical Therapy in NYC, specializing in pelvic floor dysfunction, pelvic pain, women's health, and manual therapy for men, women, and children while taking a holistic approach to each patient's entire well-being. Long story short, they consulted with her
about physical therapy treatments for vaginismus, but never talked about it on
the show as a treatment option. I
watched a video clip of the show and was sorely disappointed in Dr. Oz (not
that I ever really watched his show, he kinda creeps me out anyways). I sent Amy an email telling her I agreed with
her article about how Dr. Oz missed the mark on this one. I also asked her how I can get involved in
helping women. She gave me some suggestions and asked me to
read her book and do some online reviews.
I also wrote the Dr. Oz show telling them I was disappointed; however I
am not getting my hopes up about getting a response from them. One thing she recommended has really gotten
me excited. She told me to reach out to
Elisabeth Oas who does a weekly podcast on chronic pelvic pain, The Pelvic Messenger. What a
woman! I was able to connect with her on
the phone one day and immediately loved her! She has been through so much with her health
and I commend her for becoming an advocate and a voice for women everywhere who
suffer from chronic pelvic pain. She
suggested a few things locally that I can do to raise awareness. I am considering contacting a local news
station to see if they would be willing to do a story about pelvic pain and all
the women who suffer from it. Also, I
will be doing a short video answering questions about my vaginismus to be used
in a trailer for an upcoming documentary she is producing for PBS on chronic
pelvic pain. AND, there is the
possibility that I will be a guest on her podcast this summer to talk about my
experience with vaginismus and overcoming it!
I have also been able to up my blog exposure a little bit
with some help from friends so I’m hoping to reach women through my blog
too. I also may be helping start a
support group in the area with some women who are on the vaginismus forum that
I go to occasionally. So many things on the horizon!
If you are a woman who has pain with sexual intercourse, or
you are unable to insert anything in your vagina without pain, please talk to
your doctor. If you are uncomfortable
with that (or if your doctor tells you it’s all in your head), send me an email
and I will talk you through finding someone who can help you. You deserve to be free of this! Today, for the first time in my life, I used
a tampon. Granted, it wasn’t in exactly
far enough I don’t think so it wasn’t the most comfortable thing, but I HAD ONE
IN! I was giddy. I was dancing down our hallway. I have also been able to add in a little
something extra into my sex life because of overcoming vaginismus. I say all of this to say – YOU CAN OVERCOME
THIS TOO!
WOW! What's NOT to celebrate in this post? It's so great to hear how you have been reaching out and networking to better the lives of women everywhere. You are a true leader. Rock on!
ReplyDeleteAnd congratulations on the tampon success! That's definitely worth being giddy about. :)
P.S. Thanks for mentioning Elisabeth Oas and her podcast. I'll definitely be checking that out!
Thank you! I am really passionate about this and am doing what I can to try to get the word out there to women who are too embarrassed or scared to talk to someone about their pain.
DeleteElisabeth Oas is an amazing woman - her focus is all sorts of chronic pelvic pain, not just vaginismus. Right now she's on hiatus but I think she's coming back in April for weekly podcasts. I am just so excited to have been able to talk to her and get ideas from her on how to become an advocate.