Friday, January 31, 2014
Tearless Grief Bleeds Inwardly, part 1
Wednesday, January 22, 2014
be BRAVE! be BRAVE! be BRAVE! be BRAVE!
Saturday, January 18, 2014
BRAVE HEALING + LOVE TOUCH= MIRACLE
Wednesday, January 15, 2014
I'm no math pro, but I strongly believe: Katie + Me = Pompeii
Tuesday, January 14, 2014
Katie and Me: Reborn
Friday, January 10, 2014
Don't Let Me Down Now
Wow, well today marks one week of being on Lupron and in MENOPAUSE. I'm not sure what is causing the kind of day I had today, but I'm going to enjoy it:
~ no nausea
~ a half a hot flash
~ minimal mood swings
~ no sweats
~ only minimal cramps
Most excitingly~ NO BLEEDING!!!!!
I had an incredibly long, busy workday and am exhausted but, still, only in a little bit of pain. Put a heating pad on after a hot bath and am cuddling with my kitty.
Hoping for a continued easing up and lessening of symptoms and for a full night of deep, peaceful sleep.
Thank you for taking the time to read my blog. I'm hoping to spread awareness of this disease and what it means in the lives of everyday women AND for those women suffering with it already to know they/we are not alone in this at all.
PS this image isn't mine, I saw it in an online support group.
Thursday, January 9, 2014
Lupron: A Week in Review
WelI my first week on Lupron sure has been an emotional and physical rollercoaster!
Physically since my injection I've experienced the following:
~ night sweats
~ insomnia
~ extreme abdominal bloating
~ hot flashes
~ over sleeping
~ excruciating pelvic cramps
~ utter physical exhaustion
~ mood swings
~ menopause memory loss (like forgetting what I'm saying as I'm saying it)
~ the most random, painful pain in my left shoulder bones-- luckily not constant, it comes inwaves
~ breakouts
~ restlessness
And emotionally, I've been ALL over the place:
~ sadness
~ angry
~ frustrated
~ hopeful
~ scared
~ regret
~ overwhelmed
~ embarrassed
~ grateful
~ alone
~ misunderstood
The below picture is my second night in MENOPAUSE, which was HELL.
Saturday, January 4, 2014
Lupron baby...
Thursday, January 2, 2014
Twas the Night Before Lupron
Well, after several weeks of nearly indescribable suffering, tomorrow I'm going to to the injection center in Beverly Hills and will be having my first Lupron injection. I have gone back and forth about whether this is what I wanted to do or not. I surprised even myself by coming to this decision, for several reasons this is what I decided. First, I've been absolutely miserable and feel like I MUST do something. Second, I absolutely trust, but not blindly, my doctor- he is a genuine, knowledgeable medical professional who actually WANTS me to feel better. Third, the surgery that has been described to me is a little on the hardcore side of things and would really rather have these injections be successful than go through another surgery and recovery. Fourth, this return of endo is truly and deeply impacting my work, and that is just unbearable.
As I prepare for my appointment, I'm feeling a wide array of emotions: hope, fear, nerves, unsure, worry, sense of desperation, shame, frustration, anger, sadness, shock. I'm incredibly hopeful that these injections both improve my current condition and don't overwhelm me with unpleasant side effects. I'm afraid that the exact opposite will happen. I'm nervous about the injections themselves, I believe they were painful and burned. I'm unsure of the outcome of these injections and I'm unsure of how I can handle (physically and emotionally) an unsuccessful round of this therapy. I'm worried about how this condition will effect my life and quality of it as it continues to attack my body. With the growing symptoms and increasing nausea, pain and bleeding, I NEED this to work-- I just turned 30 this past summer and I've already had to undergo a total hysterectomy due to endometriosis. I desperately WANT/NEED these injections to help. I feel such shame with this return, as if it is some type of punishment. (Part of the reason I'm blogging is to deal with the misplaced shame I feel). I am so frustrated with every aspect of this painful disease, further frustrated with the lack of public knowledge about this disease and the cultural insensitivity to something that so seriously affects so many women-- women who should be able to be living the prime of their lives. I'm flat out angry that I have to deal with this AGAIN!!! I don't think it's fair, yes I know, life isn't fair...doesn't change my feelings though. I am sad for myself having to deal with this, and even more sad to know that millions of other beautiful women are suffering just as I am. Interestingly after several weeks of suffering very obvious and troublesome symptoms I'm still somewhat in shock that this has even returned. After having a total hysterectomy, I let myself, no matter how naively, believe it was impossible to return.
The image below isn't mine, I didn't design it, I don't intend to take credit for it or for the design, concept, etc, however I saw it on Google images and find it is so incredibly perfect to describe my sentiments toward endometriosis: