Sunday, July 30, 2017
CIZE Does Matter - A PMDD Exercise Challenge
For todayʼs guest
post, please welcome The Healthy Hackress.
Her PMDD thread will be ongoing, and I will be happy to post updates
here, but if you don't want to wait for me, please follow her journey with PMDD
and exercise either on her Facebook
page or blog. She also has a lot of great ideas for—What
else?—healthy hacks! Well worth checking
into, even if you donʼt have PMDD.
Recently I was diagnosed with PMDD. Here is my journey from
diagnosis, to treatment and more importantly, how Cize by Shaun T gave me my
life back.
According to research, PMDD affects 2-10% of women during
their reproductive years. It’s common. Very common – but misdiagnosed and
misunderstood. Thousands of women right now feel at a loss and don’t truly
understand why they don’t feel “normal” or worse, why their life literally
falls apart starting two weeks prior to their cycle. Isolation, fear and shame
are all too familiar feelings of women suffering from PMDD. I am one of them.
Do these symptoms seem familiar? Is it you or someone you love?
PMDD is a mood-based
hormone disorder that is cyclic and reoccurring. Sounds like a death sentence,
right? Imagine, every single month you know “ITʼS” coming. You’re not sure why
but two weeks prior your cycle you’re all over the place. It's like ADD meets
Bi-Polar for a 2 week fling, then they break up…until next month. You’re
clingy. You’re crying one minute, screaming the next, then sitting quietly,
unsure of WHAT just happened. Feeling a bit like Norman Bates with those “episodes.”
Seriously – that’s PMDD. If you have a significant other and
they haven’t left you already (because, PMDD truly affects all relationships) –
then you’re lucky. They feel it too – but they don’t understand.
You don’t need to wait for a medical professional to confirm
a diagnosis of PMDD – it’s self- diagnosable. You track your symptoms and
report to your doctor. This is a great tracker that you can use from The National Association for Premenstrual Dysphoric Disorder [now known as the Gia Allemand Foundation]. Basically, track how
you’re feeling before, during, and after your cycle (anxiety, mood swings,
irritability, sleep issues, etc). Your doctor is going to ask you to do this –
so, if you go in already prepared you’re that much further ahead. This process
took me 10 LONG months. Each month I tracked my symptoms so when I went to the
doctor they couldn’t turn me away and just tell me, “Everything is
normal.” If you’re living with someone
or have close friends/family – ask them to track for, or along with you. When
you’re in “IT” – it’s very difficult to emotionally and mentally report back.
Having someone point certain behaviors out can be hard – what I mean is,
someone is going to tell you the RIGHT thing at the WRONG time – because,
you’re not mentally/emotionally grounded. Try to remember – you NEED to hear
it. Their unbiased observation is going to provide necessary data for yourself
and doctor when treating YOUR PMDD.
Once I had all my data I made that initial appointment and received
confirmation that Yes, “It’s PMDD.ˮ Finally, things fell into place and I could
breathe a huge sigh of relief knowing I wasn’t crazy. Finally, someone was
listening, and everything I had felt was real & important. I had done my
research going in. I knew how PMDD was treated. I had questions on top of
questions. I needed answers. After all, my children needed their mother and I
needed myself. They started me on Yaz—reportedly the only over the counter
birth control approved for PMDD. Yes, I know—bad reviews, lawsuits, etc.—BUT,
when you’re in the Pits of Hell in the middle of a fight between Bi-Polar and
ADD—you’ll try anything to destroy their toxic relationship. I tried Yaz. After
my 2nd week both myself and my husband noticed a huge difference. I was less
spacey – more clear in my thoughts and finally felt as if I had control. Did I
still have anxiety at times? Sure, but mentally/emotionally I could WORK
through it opposed to the constant feeling of drowning. Did I have irrational
thoughts? Yes, but I was able to work through them. Yaz gave me some mental
clarity back. Unfortunately, I developed an irregular heart rate at 145 – even
when at rest. Physically, I was breaking down. After an ER visit and a couple
visits to the Dr. – I came off of Yaz.
Then I tried Zoloft. *sigh* If you know me – I’m ALL natural—from
giving birth naturally to treating headaches with almonds. I’m not huge on
medication unless it’s NEEDED. “Well,ˮ I said to myself, “I have to try everything
so I know at the end of the day – I did my best.ˮ 3 days later I caught myself staring out my
window watching birds & not caring that I was sitting there staring out a
window – Kathy Bates from Misery
anyone? The things that once made me laugh no longer put a smile on my face. I
wasn’t OK with that. I knew I wasn’t ME – bubbly, personable, caring – I wasn’t
me. I was only on 25mg and that’s not even the therapeutic recommended dose of
50mg for Zoloft. I then safely decreased (with the support of my Dr.) to 12.5
and discontinued it. Wasn’t for me. That isn’t to say that someone else may not
greatly benefit from SSRI’s.
Currently I’m on a different form of HRT (Hormone
Replacement Therapy) – Continuous Birth Control, which would halt the dramatic
changes in hormones and provide balance. I will need to report back on this as
this is my newest form of treatment. Along with the birth control I’m taking a
Vitamin B Complex, Daily Multi for Women – I Prefer Rainbow. Natural. Plant
based. Also, I’ve added 2 TBSP of Ground Flax Seed to my oatmeal in the
morning. According to research, Flax Seed can mimic the female hormone Estrogen
and provide other benefits such as relief from Depression. In my search for
Vitamins and Minerals that could/would provide potential relief from PMDD – I
came across some great work by Dr. Mark Hyman – He’s truly fantastic. I’m a
Certified PLATE by Zumba Instructor and he provided some of the training. Here
is a great article he wrote with vitamins and remedies in helping to relieve
PMS/PMDD.
Now, you ask “Why does Cize Matter Again?” I woke up one
morning very early. I couldn’t sleep and was just DONE with doctors not knowing
how to help. Done with being turned away. Done with being told “Everything is
normal.ˮ I was just done. From one failed medication to another I had it and
wanted/needed to take control back. Then I watched the infomercial for Cize. I
asked my husband to get it for me because I was willing to try anything to get
my new self and leave my old self behind. He did. I was nervous and hesitant. After
all, I had tried Insanity and Shaun T delivered. He kicked my A$$ and that felt
good. This time around I knew I needed something a bit more “me” – this was it.
Cize gave me that. From the minute I played the first day I was hooked. Losing
weight and becoming a size 5 was no longer relevant. Waking up everyday knowing
I could beat my anxiety became my goal.
Each day it became easier. I felt a bit better. I still had
the PMDD symptoms – but mentally, I felt stronger than ever. Shaun T will never
truly understand what he helped me get back. I’m in week 4 and I feel better. I
look forward to my routines with him because I know he’s right there telling me,
“You got this.” I know missing a day isn’t acceptable. Each day Cize is my
Zoloft, except I don't suffer from any side effects – like staring out a window
for 20 minutes or losing the ability to laugh at everything that once brought a
smile to my face.
Some women may need some additional SSRI as a support. Please
don't take my experience as true for everyone. Don't be ashamed. Each and every
woman needs to find THEIR treatment because PMDD for one is VASTLY different
for another. Listen to your body and
remember – doctors aren’t always right. Be your own doctor and researcher. Keep
a journal of symptoms and never, ever – stop fighting.
This thread will be ongoing. I will keep everyone posted on
my 60 day Cize challenge that I intend on making a routine for the rest of my
life. Each day I laugh more, feel the fight harder and see the results I’ve
been looking for all along. Mental and emotional health are far more important
than your physical appearance. That will come in time. Nourish your soul and
show yourself everyday that you matter – release those feel-good hormones
because exercise and movement is truly the first line of treatment for any
disorder.
Don't be ashamed to share your story, ask questions and or
seek support. If it isn’t a fight and doesn’t hurt getting it, it isn’t worth
it. Fight hard. Remember, it isn’t about the scale, it’s about how you feel!
If you know someone presenting with PMDD symptoms. Reach
out. Don’t push them away. Be a support. Share this blog. The biggest and most
deficient need of women suffering from PMDD is support. The National Association for Premenstrual Dysphoric Disorder provides great support.
Thank you Shaun T for being there & giving me the
strength to fight back.
Thursday, July 13, 2017
Friends and Family Guide to PMDD -- Things NOT to Say
The following guest post was written by the blogger Cheekyminx. With
her permission, several of her posts about PMDD are being featured on this
blog. To find out more about her work as a PMDD Advocate, please visit her
Facebook page, PMDD Life Support.
This post is for friends and family who
want to be supportive of a woman with #PMDD. Here, we've covered things you
should NEVER say, out of compassion. No doubt many of you may feel that it
doesn’t matter what you say; it’s going to be wrong.
Sure enough, a couple of women responded
to our question about what not to say by affirming that everything ticks them
off at certain times of the month, so for some of you, your feelings may be
justified.
Still, certain words can be hurtful, or
even triggering, for a woman grappling with PMDD, whether or not she’s having
symptoms. We don’t want to be stigmatized when we’re feeling good nor punched
when we’re already down. While it is true that ultimately, our responses to any
comments are our responsibility, not yours, those of you wanting to be more
understanding towards us might want to abstain from the following phrases.
Once again, we asked women on various
PMDD forums for their input. Once again, many of them reported very similar
comments as annoying, offensive, or triggering. We’ve analyzed and categorized
them to show the types of comments that are counterproductive; there could be
many more variations under each heading. Statements in parentheses represent
the internal thoughts shared by women on the forums. Depending on how these
comments are delivered (and the level of your frustration when delivering
them!), they can simply be insensitive or invalidating, or downright cruel and
abusive. Do any of these sound like you sometimes?
Self-Anointed
Diagnostician
“Is your PMDD here again?” or “Are you
on your period?” (as if that explains away legitimate complaints)
“Is it that time again?”
“You must be: bi-polar, borderline,
psycho, sick…” or “You need: professional help/to be committed.”
“Oh!!! You got your period then??”
“You are: crazy, mental, nuts…”
“Did you take your tablets today?” or
“Have you taken your meds? Maybe you should take 2!”
Just
Get Over It
“Calm down!” or “Just control it!” or
“Relax.”
“Your being dramatic; it’s not that big a
deal,” or “You’re overreacting,” or “You’re just PMS-ing.”
“You’re so problematic… Why don’t you
control yourself?”
“You’re being ridiculous! Are you mad?”
“Be rational. It doesn’t make sense to
get so upset over something so small.”
“Stop bitching,” or “Stop being a
bitch,” or “Just stop!”
“It will pass.” (Yes, I know. But right
now, I need understanding. I feel like shit!)
Now
What?
“What is wrong with you now?” or “What’s
wrong now?”
“You were fine a few minutes ago,” or
“Suddenly you’re in a bad mood?”
“Christ, here we go again!”
"Great. Now what are we supposed to do?"
Please
Explain the Inexplicable
“Why are you: depressed, sad, angry,
mad…?”
“Is everything okay?”
“Why can’t you explain what’s wrong?”
“Are you mad at me?” (if only it was as
simple as being “mad at you”)
Just
Harsh
“Same old excuse!”
“PMDD isn’t legitimate.”
“You are possessed!”
“You’re just lazy.”
“I can’t stand to be around you,” or “I
can’t stand you when you’re like this.” (Great, that makes two of us!)
As I’ve said before, each of us is
unique, so use this list to start a conversation with your
partner/friend/sibling/daughter/girlfriend/wife during the good days. This way,
when the bad days roll around, everyone is prepared…well, as prepared as
possible anyway.
In summary, please don’t tell us to
“calm down”, “get over it”, or “cheer up”. You’ll only be asking for a fight.
If we could calm down and get over it, we’d already be calmed down and over it.
Please do not call us “mental” or “crazy” or any other derogatory term related
to our mental health. And for God’s sake, do not go around diagnosing us with
mental disorders we don’t have. We may very well be acting like we’re nuts, but
believe me…we are aware of this and DON’T need the reminder.
Finally, remember that we’re human. And
like all humans, we still get angry and have a full range of emotions even when
we don’t have PMDD. So please don’t blame everything on PMDD. We can’t. You
shouldn’t be allowed to either. .
So, what do you think? Have we got it
covered or is there something YOU would like to never hear again?
Subscribe to:
Posts (Atom)