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2/27/2009

'Jeanne's Endo Blog': March is National Endometriosis Awareness Month

I saw this link thanks to Sandy Robinson listing it on the Fighting Fatigue blog.

It's so great to see endometriosis awareness increasing!!! This link gives the history on when National Endometriosis Awareness Month officially started being observed.

March is National Endometriosis Awareness Month
Endometriosis is a chronic condition that affects over 5.5 million women in the United States and Canada.

March is National Endometriosis Awareness Month

If you pull up the above link, you'll see that you can comment to it (as I did there) and you can "share" it (as I just did by posting the link above on Facebook).

Let's all work together to increase endometriosis awareness. Reading the link above, commenting, and linking it to Facebook probably took me all of 3 minutes total. Won't you join me in sharing this link?

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

"Jeanne's Endo Blog" Thanks Melissa Ralston Of "Endometriosis: Facing The Battle Head-On"...

Thank you to Melissa Ralston for the shout-out about my endometriosis awareness petition and our efforts to attract media attention to the importance of getting endometriosis FACTS out to the public.



Here's her post:

Raising Awareness: Media Campaign for Endometriosis Awareness Month (March)

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

2/26/2009

'Jeanne's Endo Blog': Hysterectomies Are Over-Performed In The U.S. ---- My Comment Posted On The February 26th Newsweek Article "Female Trouble"...

This post is in regard to a Newsweek article about hysterectomies.

Today I received a Google alert for an article related to the search term "endometriosis".

The article is called "Female Trouble".

To be honest, I've never been a big fan of the phrase "female trouble". After all, when men have prostate problems or testicular cancer, no one goes around labeling it "male trouble", right??

So this Google alert got my attention with the title of the Newsweek article alone.



While I wasn't so crazy about the title, I was pleasantly surprised by this article:

"Female Trouble"


Here is the comment I posted on the Newsweek site in response to this 2/26 article about hysterectomies:

Newsweek is to be congratulated (!) for educating the public that hysterectomy decisions are serious and permanent!

This article wisely takes note of the fact that too many hysterectomies are performed in the U.S.

I have met women who have had hysterectomies in the hope that it would help them feel better (with their endometriosis symptoms), only to proceed to have further, serious problems AFTER a hysterectomy! Their doctors led them to think they’d get relief that did not happen. The grief this caused them emotionally on top of the persisting physical problems is significant! Once your uterus is gone, it’s gone. There’s no going back.

Deciding to have a hysterectomy is a very serious decision to make.

Patients, don't be afraid to seek out a 2nd or 3rd opinion if a doctor suggests you get a hyst.

My local support group members have found this organization (see below) helpful for researching alternatives to hysterectomy. This site is a resource for any woman considering having a hysterectomy (not just endometriosis patients).

HYSTERECTOMY ALTERNATIVES AND AFTEREFFECTS
HERS FOUNDATION: Hysterectomy Educational Resources and Services


I have had doctors talk about hysterectomy as an option for me over the years, due to my endometriosis and other GYN conditions. (I am 40 years old and my endometriosis started at age 13). I have elected not to have a hysterectomy for a variety of reasons. (There is no cure for endometriosis, by the way).

Many people believe hysterectomies cure endometriosis. That is a MYTH.

I would urge women thinking of having a hysterectomy to research your options and seek out multiple opinions BEFORE jumping into a hysterectomy.

As this article concluded:

Hysterectomy IS a serious and permanent decision.

Thank you, Newsweek, for letting people know MORE about hysterectomies than they might have before they read this article!

Jeanne
Blog address: Jeanne's Endo Blog
* March is ENDOMETRIOSIS AWARENESS MONTH!!! *

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

2/24/2009

"Jeanne's Endo Blog": Endometriosis Awareness (Vlog Post 2)

Our campaign is making progress! If you have not seen the related posts preceding this from 2/16/2009, 2/20/2009, and 2/23/2009... please see links at the end of this post so this one will make more sense.

Welcome to my second vlog!

THANK YOU you for the warm welcome on the first one... the most comments I've ever had to one blog post!

The video clip below will update you on our endometriosis awareness campaign status: our awareness petition, our letter-writing campaign, our variety of efforts to seek media attention regarding endometriosis facts, and our preparation for Endometriosis Awareness Month.



Video is copyright © 2009 Jeanne's Endo Blog. All rights reserved.

In preparation for Endometriosis Awareness Month... I am asking endometriosis patients, bloggers, and anyone else interested in the endo cause to please contact Donna Jackson Nakazawa (contact info for her blog address is in link below).

Also, would all twitter users please include this symbol at the end of all endometriosis-related tweets?

#endo

You may have noticed other bloggers using similar hashtags...

Such as "The Spoon Lady" from:

But You Don't Look Sick?, written by Christine Miserandino.

Christine uses the symbol: #spoonie

By using #endo, we will be able to search twitter for endo-related tweets. So will anyone who uses twitter and makes use of it's search function.

Granted, with a 140-character limit per tweet, sometimes it may be a bit challenging to fit the extra 5 characters. However, this will code enable us to sort/search for the tweet messages we need more quickly & effectively and it will catch the attention of others to the endo cause.

If you haven't already done so, please comment on Donna Jackson Nakasawa's blog (see link below for her blog and info about contacting her! :)

Related links:

Monday, February 16, 2009 Jeanne's Endo Blog: How MORE Magazine’s Chronic Illness Article Knocked My Socks Off & How Happy I'd Be If We Can Work Together To Get Endo Covered!

Friday, February 20, 2009 "Jeanne's Endo Blog": *ENDOMETRIOSIS AWARENESS* Letter Campaign Example!!

Monday, February 23, 2009 "Jeanne Endo Blog" Honors Donna Jackson Nakazawa, Author Of The "Ill In A Day's Work" Article In The Feb 2009 Issue Of More Magazine!

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

2/23/2009

"Jeanne Endo Blog" Honors Donna Jackson Nakazawa, Author Of The "Ill In A Day's Work" Article In The Feb 2009 Issue Of More Magazine!

I'm so happy; I feel like I just won the lottery!

I just found a blog for Donna Jackson Nakazawa!




She is the writer of the phenomenal chronic illness article that launched our endometriosis awareness campaign back on February 16, 2009:

Monday, February 16, 2009 Jeanne's Endo Blog: How MORE Magazine’s Chronic Illness Article Knocked My Socks Off & How Happy I'd Be If We Can Work Together To Get Endo Covered!



Donna Jackson Nakazawa is also the author of a book: "The Autoimmune Epidemic: Bodies Gone Haywire in a World Out of Balance -- and the Cutting-Edge Science that Promises Hope"

Upon discovering her blog, I felt compelled to write her and thank her for that amazing article referenced in my 2/16 post:

"Ill In A Day's Work"

Here's my letter to Donna Jackson Nakazawa, posted on Donna's Blog
--->
Hi Donna!

I am SO happy I found this site! If your ears are ringing it’s because I have been singing your praises on my blog!

Your “Ill in a day’s work” article for More magazine’s February 2009 issue is PHENOMENAL!!! I cannot say enough about it. I’ve written on my blog about it! I posted my first vlog (video) entry and even held up your magazine and just plain raved about the article.

Having numerous chronic illnesses, many of which are autoimmune conditions… I LOVED your thorough article!

The first chronic illness to hit me was endometriosis, at age 13. I’m 40 now. So I have dealt with endo for 27 years.

In that time, I’ve participated in local (in person) endo support groups since 1992 (after my diagnosis, which took TEN years from onset of symptoms). I started an endo group, as a volunteer support group leader, in my current community in 2001. I started my blog last June.

My career went up in smoke several years back. I was far too sick to function.

I have heard hundreds of women’s stories… Not just with endometriosis but with others illnesses (many connected in studies to endo)… For example, fibromyalgia, IBS, interstitial cystitis, Reynaud’s Disease, multiple chemical sensitivity (MCS)… [I have all of the above diagnoses... and other conditions].

My blog is about chronic illnesses. Mariela Azcuy of Meredith Corp. has emailed me publicizing your chronic illness article after seeing my blog.

Since then, I have organized a letter-writing campaign to find a way to get endometriosis featured in the national media. It affects 89 MILLION women and girls. It can affect careers, marriages, fertility, severe chronic pain… It has a huge impact on patients and their families.

I have had 7 surgeries for endo. I have too many other illnesses to count at 1:40 am when I should be asleep…

I just want to thank you for your More article so much!!! I literally held up the magazine in my vlog post on 2/16 on my blog… and asked people to buy it for YOUR article.

I would be honored if you’d take a moment to check out my blog post *about your article*!

I don’t normally post links in blog comments and I’m NOT trying to be spammy but I’m listing the specific link that will route you to the More magazine post with your article:

http://endendoat.blogspot.com/2009/02/jeannes-endo-blog-how-more-magazines.html

If you read the blog comments section, you’ll see where I talked about the fact that I would “jump up and down” if we in the endo patient community were fortunate enough to have a writer well-educated about chronic illness (such as you) write a feature on endo!

Endo affects 89 MILLION women & girls. That’s more than breast cancer!

I would be deeply honored if you’d read/view my blog entry from 2/16 about your article.

THANK YOU (!!!) from the bottom of my heart for that More article! Looks like I need to add your book to my very large reading list. There are never enough hours in the day for me to read my mountain of books.

Take care and I’d be thrilled and honored if you check out my blog.

Also you can email me directly at:

endendo [at] frontiernet [dot] net

I just wrote it out to minimize spam. I learned awhile back that the Google robots and such find online posted email address but this helps. Just remove the spaces, replace [at] with the @ sign, and replace [dot] with a period… and delete the spaces.

I very much look forward to connecting with you!

Jeanne


Please join me in thanking her for this outstanding article and please also join me in asking for her assistance in helping us find a national voice for endometriosis, which affects 89 MILLION women and girls worldwide... more than breast cancer.

Let's thank her on her blog and let her know how much we appreciated her article on chronic illness! Let's let her know that we would be deeply honored if she'd consider writing an article about endometriosis!

In honor of the upcoming March Endometriosis Awareness Month, let's make our voices heard and spread awareness!

Related links:


Monday, February 16, 2009 Jeanne's Endo Blog: How MORE Magazine’s Chronic Illness Article Knocked My Socks Off & How Happy I'd Be If We Can Work Together To Get Endo Covered!

Friday, February 20, 2009 "Jeanne's Endo Blog": *ENDOMETRIOSIS AWARENESS* Letter Campaign Example!!


Thank you.

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

2/21/2009

"Jeanne's Endo Blog" Featured On Google Alerts... Plus A Nature Break And Intro to HolisticTwitter!

I thought I'd start out with these beautiful pictures. They are courtesy of Debby Bruck... a member of the HolisticTwitter group I just joined!

Andrea Tannouri will give you a warm welcome there! It's a cool group. Check it out!

Enjoy...


Find more photos like this on HolisticTwitter.com

I was pleased to receive the second Google alert in two weeks featuring my blog!

On 2/6, the Google alert email featured this link (which was a bit outdated when the alert went out):

Wednesday, November 26, 2008 'Jeanne's Endo Blog' Is Featured In Interstitial Cystitis Association's Newest Cafe ICA Newsletter!!

On 2/21, the Google alert email featured this link (which is a brand new post):

Friday, February 20, 2009 "Jeanne's Endo Blog": What Can I Expect From Having A Laparoscopy???

I am honored that Google alerts for two of my blog posts have been sent out since February 6th!

Have a great weekend!

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

2/20/2009

"Jeanne's Endo Blog": *ENDOMETRIOSIS AWARENESS* Letter Campaign Example!!

This post is a follow-up to:

Monday, February 16, 2009 Jeanne's Endo Blog: How MORE Magazine’s Chronic Illness Article Knocked My Socks Off & How Happy I'd Be If We Can Work Together To Get Endo Covered!

If you haven't yet read the above post, I encourage you to do so.

Following that post, Endochick and I discussed how we can capitalize on the momentum we have going to get people writing letters for endometriosis awareness. I asked Endochick if I could reprint her amazing letter to Mariela Azcuy (see Ms. Azcuy's contact info later in this post):

Endochick graciously agreed to let me print her letter to Ms. Azcuy. Whether this letter was written to Ms. Azcuy or to anyone with media contacts, we believe that posting sample letters such as this will inspire others to write their own letters regarding their personal journeys with endo!

March is Endometriosis Awareness Month. We're ramping up now to, hopefully, make a big splash next month regarding endometriosis awareness!

I urge you to read Endochick's post from today:

*ENDOMETRIOSIS AWARENESS* Letter Campaign Example!!

Her post about this topic on her blog gives much helpful detail!! So please go check it out!!

Now, it is my pleasure to present Endochick's letter. Again, I urge you check out Endochick's entire post about the topic of letter-writing to create endo awareness... especially with Endometriosis Awareness Month around the corner in March!!

As promised, here is the example of Endochick's letter to Mariela Azcuy. Please remember that her work on her blog is copyrighted and that the following letter is therefore under copyright protection (as is my writing on this blog).

Endochick says,

"You may use this example as a reference, and I hope it inspires you".



Endochick

Here's Endochick's "Sample Letter":

---

Mariela Azcuy
Senior Associate Director of PR
Ladies’ Home Journal, More and Siempre Mujer Magazines
Meredith Corp.
125 Park Ave, 17th Floor
NYC 10017

Dear Ms. Azcuy:

I am writing on behalf of the 89 million women and young ladies who suffer daily from endometriosis. In North America it’s estimated that this number is 5.5 million strong and growing every year. Many of these women go undiagnosed for years and then once diagnosed are either under or improperly treated. And even worse, Ms. Azcuy, endometriosis sufferers are marked with a stigmata that haunts them, often before they are even officially diagnosed with the condition. Society views many of us as drug seekers, doctors withhold needed medication, and our co-workers and bosses see us as attention seekers.

But let me first commend your corporation for its in-depth coverage on chronic illnesses. While these illnesses do warrant a need for more press time, one chronic and often time debilitating illness is not getting it’s due coverage in the media – endometriosis. This past fall, television viewers received a mediocre education on endometriosis via the coverage given to Dancing with the Stars’ Julianne Hough and Lacey Schwimmer’s diagnoses’.

The coverage by the media glossed over one vital fact in how endometriosis is diagnosed: the only definitive way to diagnose endometriosis is to perform a laparoscopy. According to the Endometriosis Association, “diagnosis is considered uncertain until proven by laparoscopy, a minor surgical procedure done under anesthesia. A laparoscopy usually shows the location, size, and extent of the growths. This helps the doctor and patient makes better treatment choices.” The Endometriosis Research Center agrees: “Endometriosis can ONLY be diagnosed via surgery; diagnostic tests like MRIs and ultrasounds are not definitive.”

The scary fact is that there are doctors diagnosing patients not with “probable endometriosis” but with “definite endometriosis” based on nothing more than their symptoms. The diagnosis from one to the other allows the doctor to prescribe a whole host of potent medications; medications that should be reserved for women with confirmed endometriosis that doesn’t respond to lesser hormonal preparations. Yet, I have personally seen this happen with two women who have contacted me via my blog. They hadn’t even had a laparoscopy, so their doctors can’t even be sure they in fact do have endometriosis! It was believed that my own sister had endometriosis until a laparoscopy found her pelvis free of the disease. A pap smear, on the other hand, found the cause of her excessive bleeding: cervical cancer.

There are too many conditions that can mimic endometriosis - diverticulitis, infection, ovarian cysts, pelvic inflammatory disease, irritable bowel disease, STD’s, vaginitis, and even ectopic pregnancy. Would it be ethical to give anti-cancer drugs without first doing an MRI or a CT scan to look for a tumor? Yet, there are doctors subjecting women to the effects of menopause, severe migraines, moments of rage, and a decreased sex drive when an outpatient, surgical procedure can determine whether there is even a need for the medication!

As I hope you can see there is an urgent need for appropriate, in-depth media coverage on endometriosis. My fellow endometriosis and chronic health bloggers congratulate your corporation on the wonderful coverage you’ve given to the chronic illness community, now we implore that you do the same for the endometriosis community. Please help me and my fellow endometriosis bloggers to help the 89 million women and young ladies feel that the pain they feel is not in their minds, and that they are not alone. Help us to give endometriosis the voice it deserves in the media.

Sincerely,

Endochick (Put your real name)

Blog:
Endometriosis: The Silent Life Sentence

------

My hope and intention in the coming weeks is to post more sample letters to inspire YOU to write your stories to get the facts about endometriosis into the media once and for all.

Please keep those letters rolling into Ms. Azcuy and I'd really appreciate if you can copy me on them if at all possible!! If you copy me on your letter to the press (Ms. Azcuy or otherwise), please indicate whether you'd be comfortable with me posting your letter as a sample to inspire others to write in to support accurate media coverage of endo!

The response to the vlog/blog post has been fantastic. Please keep those letters and petition signatures rolling in. :)

Thank you!

This post is cross-posted with Endochick's post:

*ENDOMETRIOSIS AWARENESS* Letter Campaign Example!!

This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

HAVE YOU SIGNED YET?? Please Sign Endometriosis Awareness Petition Below! Awareness YEAR-ROUND!