I think I am going to register to raise money and if I raise at least the minimum I will be able to take part in the walk that will happen September 11th 2011 in Toronto, now I just have to finish my registration and try to raise lots of money.
For me I think it would be great to raise enough money that I can take part in the walk (the walk is 60km if you sign up for 2days, or 32 for one day and I am thinking 32km would be pushing it, so that’s the one I am signing up for) but even if I just manage to raise money to help I think that will be enough to make me happy.
From the website:
"All of this is made possible because of people just like you! Be a part of our celebration on September 10-11, 2011 and customize the best Weekend experience for you. Choose to enjoy the full 2-Day, 60km distance for maximum impact, or try the 1-Day 32km distance. You can also designate your fundraising dollars to go specifically to breast cancer or gynecologic cancers. Whichever experience you choose, make YOUR Weekend matter!"
To be able to take part in the walk I will have to raise $1250, so once I have all the paperwork done and am able to start collecting the money I will be sharing the website they will give me to help me share and fundraise for a really good cause.
As someone with endometriosis me and all my endo sisters are at an increased chance of having many of the women’s cancers (largely in part since we can’t always have children and those who never have a child are often at a greater risk).
Then there is the reality that not only do many of these cancers affect so many people but have affected people very near and dear to me so I would like to walk in a way for them (both those who are still here thankfully, and those who we have all lost).
Just thought I would share all that.
And in other news, I still have the Mirena in and it is still seeming to get better and better as time goes on, though I think I am on my “period” now (key word that makes me happy in that sentence was think haha) I am having some more cramping then my normal day to day and am also spotting, and with an IC flair happening it seems to be making sense.
Though as a reminder to those who know me and my family the fact I have the Mirena IUD is still hush hush please and thank you. In time I will share it with everyone who might want to know, but I am betting that will be closer to the 6-8month mark and right now I am almost at the 4month mark so it will take yet. They key is I don’t want to share until it has done crazy wonders for me and although it has already helped greatly it hasn’t made my day to day pain disappear and I am hoping it will in part and once it does I can brag I am on it for it will my little miracle piece of plastic in my uterus haha.
I live in chronic pain. The reason for my pain, is Endometriosis. I was diagnosed through surgery when I was 17. I have decided to have this blog, so that those in my life can get a peek into my day to day issues that affect my life in every way.
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I live in chronic pain. The reason for my pain, is Endometriosis. I was diagnosed through surgery when I was 17. I have decided to have this blog, so that those in my life can get a peek into my day to day issues that affect my life in every way.
Showing posts with label Mirena. Show all posts
Showing posts with label Mirena. Show all posts
Monday, March 28, 2011
Thursday, December 16, 2010
Writen December 16 2010
If you are someone who knows me and talks to other family of mine please read this and forget it, or keep it to yourself.
The things I am about to say in here few people know about and those people DO NOT include my parents or family in general.
I wrote this then decided to hold off posting this till I knew how my body seemed to be handling the new treatment.
(Written December 16 2010)
One week ago today I went to the doctors, a GYN and started on one "medication" to try to help out with my endometriosis. It’s a last resort treatment but it is better than the other alternative last resort things that are also not guaranteed to pan out (like a hysterectomy I have no intention of trying anytime soon).
This treatment is also a birth control used by many women it is known as the Mirena IUD.
It’s been one week ago today that I had it inserted and insertion was painful, but insertion doesn’t take that long, though I had extra pain since even the speculum hurts but I got through it holding S's hand and looking up at the ceiling reading and rereading the comics (this doctor has doctor related comics on the ceiling so when your being examined you have a distraction, its awesome).
The medication you insert the night before you have the IUD inserted started me cramping within an hour but I was able to cope with it. The actual insertion did hurt allot and I was vocal about it, though I was medicated so wonder how much worse it could have been if I had only taken Tylenol like he had suggested (I was on dilaudid, and a bunch of herbal sedatives along with gravel since I know pain makes me throw up at times). I expected bleeding after insertion but that never really happened yes, I had one really small clot at that was it. However the cramping after insertion is still happening I am hoping it will settle down.
The things I am about to say in here few people know about and those people DO NOT include my parents or family in general.
I wrote this then decided to hold off posting this till I knew how my body seemed to be handling the new treatment.
(Written December 16 2010)
One week ago today I went to the doctors, a GYN and started on one "medication" to try to help out with my endometriosis. It’s a last resort treatment but it is better than the other alternative last resort things that are also not guaranteed to pan out (like a hysterectomy I have no intention of trying anytime soon).
This treatment is also a birth control used by many women it is known as the Mirena IUD.
It’s been one week ago today that I had it inserted and insertion was painful, but insertion doesn’t take that long, though I had extra pain since even the speculum hurts but I got through it holding S's hand and looking up at the ceiling reading and rereading the comics (this doctor has doctor related comics on the ceiling so when your being examined you have a distraction, its awesome).
The medication you insert the night before you have the IUD inserted started me cramping within an hour but I was able to cope with it. The actual insertion did hurt allot and I was vocal about it, though I was medicated so wonder how much worse it could have been if I had only taken Tylenol like he had suggested (I was on dilaudid, and a bunch of herbal sedatives along with gravel since I know pain makes me throw up at times). I expected bleeding after insertion but that never really happened yes, I had one really small clot at that was it. However the cramping after insertion is still happening I am hoping it will settle down.
Labels:
Back pain,
cramping,
endometriosis,
IUD,
Mirena,
Mirena IUD,
spotting
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