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Showing posts with label Endometriosis Assn.. Show all posts
Showing posts with label Endometriosis Assn.. Show all posts

11/14/2008

Endometriosis Blog: "Endochick" Is Today's Guest Blogger On The Topic Of The Endometriosis Awareness Petition and Dancing With The Stars!

Meet Endochick.



She writes Endometriosis: The Life Sentence. I have followed this blog for quite awhile. It is fantastic!!

To date, we have 171 signatures on the petition referenced below to create awareness of endometriosis... Feel free to sign it if you like!

Endochick's witty sense of humor, great insights, and educated comments always keep me coming back for more. Endochick has given me permission to reprint her blog post from yesterday as a "Guest Blogger" post here today. What follows is her post from November 13, 2008. I greatly appreciate her allowing me to re-post it here and encourage you to check out her blog. For more of Endochick's endometriosis writings laced with an amazing sense of humor and the sad truths about what living with endo can be like, I encourage you to check out her consistently high-quality blog.


Endochick's "Dancing With the Stars - Endometriosis" post from her blog Endometriosis: The Life Sentence:

While I don’t watch this show, I have heard about the controversy surrounding two of the stars’ recent admittance of having endometriosis. The first being Julianne Hough’s. She is quoted as saying, “They want to clean out the cysts and take out my appendix, too, because later on it can be affected by the cysts.” I’m assuming - in this case - if these were endometriomas then there would be no need for a diagnostic lap because the doctor would know what she had. I’m sure, with the money that doctor is probably charging in Hollywood, a CA125 was done to rule our cancer for those thick walled cyst since she hadn’t already had confirmed endometriosis. Thus, leaving only a diagnosis of endometriosis and no need for a diagnostic lap. Still though, from a public relations perspective - it would’ve been wise for her to stay mum until after the surgery and then come out with her diagnosis since both the Endometriosis Association and Endometriosis Research Center say a laparoscopy is the only definite way to confirm endometriosis.

Now, Lacey Schwimmer is another issue. She is quoted as saying, “I went to go get checked out today and I actually have the beginning onset of what Julianne has, which is endometriosis, and it hurts very bad,” admits the dancer. “Right now I’m insanely weak, and the room is spinning.” If her doctor suspected she had endo, he should have put her in for a lap to diagnose it and clean it out, and help her pain and weakness (which I assume is from blood loss). The earlier endometriosis is diagnosed the better the outcome for the patient! Just tossing an endometriosis diagnosis onto every painful period or heavy period can be dangerous, and I’ll get into that after I offer two quotes below:

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 make better treatment choices”.

Endometriosis Research Center: ”Endometriosis can ONLY be diagnosed via surgery; diagnostic tests like MRIs and ultrasounds are not definitive”.

Now, with that being said: While endometriosis can ONLY be diagnosed definitely by a laparoscopy, doctors will often go on patient history coupled with family history, and symptoms and give a “possible diagnosis of endometriosis” or “suspected endometriosis.” Why is this important? Because there are a few medicines that insurance companies will not pay for until a laparoscopy has been done to confirm endometriosis. Until then, a doctor cannot use medicine like Danazol or Lupron to treat “suspected endometriosis.” I had “suspected endometriosis” for over 10 years. My doctors were sure that’s what I had based on my symptoms, what medicines worked and didn’t work, and the fact that my mother had it and my aunt. BUT even they told me it couldn’t be confirmed until I had the lap.

NOW - why do the EA and ERC and the American Medical Association (AMA) call for laparoscopy to confirm the presence of endometriosis in order to make the diagnosis? That is because there are a host of pelvic and abdominal maladies that can mimic the disease, and often endometriosis sufferers suffer from at least one of them as well (i.e. IBS).

These are:

Infection - this is especially true if your symptoms come on suddenly and out of the blue

Diverticulitis

Irritable Bowel Syndrome

Inflammatory Bowel Disease

PID

Vaginitis and BV

STD'S

Functional Ovarian Cysts

Ectopic pregnancy

Do you see the need for the laparoscopy protocol???

Let me provide a real life example of the importance for DIAGNOSIS:

My sister, she was 22 when this occurred, began bleeding profusely. Soaking pad after pad, months rolled into one after the other until she went three month without a single break in her period. That’s three months without a day where she didn’t bleed. I never had excessive bleeding with my endometriosis - mine is all pain. My mother, though, bled constantly. My mother told my sister that that was how her endometriosis started. Since my sister couldn’t get into the doctor right away, she felt she could wait another two months through this hell of constant bleeding until her annual exam. At her annual she described what was going on, her family history, etc. Her doctor said that it could be endo since my sister did have a history of some nasty periods and had a failed marriage because they tried for 2 years to have a baby and couldn’t get pregnant. My sister asked to be treated, doctor said all I can give you is a depo shot to stop the bleeding because it’s not confirmed. They agreed to see if that would stop the bleeding first because my sister didn’t have the time at work to take for surgery. Meanwhile, her pap results came back - she didn’t have endometriosis…. her bleeding was from cervical cancer.

I am not discrediting the fact that the women have endometriosis. I am sure they do and feel horribly for them. No one should have to get this disease. It’s a terribly chronic malady that needs a cure. It afflicts too many women! We should stop bickering and band together to fight this! That was the point of Jeanne’s petition. Endometriosis is getting attention right now because of the DWTS’s celebrity, but the wrong message is getting out there. Her petition is simply calling for more media coverage of the FACTS. And we need that. How is this disease DIAGNOSED and TREATED? Let’s get that covered on Oprah. A whole show devoted to it. Could you imagine the women we could reach in that ONE HOUR? Women who are sitting on there couches, laying on their beds, in pain pain, curled into balls, slaves to their heating pads, drugged on pain killers? We could reach them with a message of hope, a message of “there may actually be something wrong with other than just a painful period.” We could give them reassurance that it’s not all in their heads. There is nothing wrong with living with a “suspected endometriosis” diagnosis, especially if you’ve ruled out the biggies that could kill you. But the lap can confirm, open up pathways to better treatment, and can give you that “I told you so” leverage we endo sufferers need when we are laying curled up on the couch knee deep in tissues.

Please, let us stop this bickering and sign Jeanne’s petition. You can find it here:

Create Awareness & Understanding About Endometriosis

There is nothing wrong with more awareness and education when it comes to this disease - or any disease.

Let me finish by saying I do not discredit that either DWTS woman has endometriosis. I am not their doctor, nor do I have access to their personal medical records. I am just going off of how they are presenting their endometriosis to the public. As celebrities they have a responsibility to their fans to be responsible with their words. Before saying they have a disease or illness, they should make sure they have been accurately diagnosed with that disease. There are some diseases and illnesses that if a celebrity came out and said they had without a diagnosis, there would be a backlash - i.e. cancer. Could imagine if Christina Applegate had come out and said “Well, I felt a lump and knew it was cancer so I announced it as such before I had a mammogram.” No, she had a mammogram and a biopsy before she announced to the public that she had breast cancer.

People who suffer from diseases, especially chronic diseases, do not take it lightly when someone comes along and willy nilly says they too suffer from it without proper diagnosis. A doctor should always be cautious and add “suspected” or “likely” before a disease or illness until it is confirmed.

Related link (that contains MANY other related links):

Saturday, November 8, 2008 Endometriosis Blog: Endometriosis Awareness Petition Will Be Sent This Weekend To Oprah And The View

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

7/03/2008

Endo Blog: Holidays Can Be A Bit Challenging

As we head into a holiday weekend for those of us in the U.S., many are thinking of summer fun: barbeque cookouts, picnics, pool time, visiting with relatives, traveling, etc.

Holidays can also be an emotionally challenging, if not painful, time for chronically ill patients. Sometimes friends and relatives can have expectations of their chronically ill loved ones that are not realistic.

A chronically ill patient/chronic pain patient (endometriosis induced or otherwise) often cannot "keep up" with healthy peers on everything expected of them.

This can cause hard feelings, misunderstandings, tension, and isolation.

Some chronically ill patients push themselves HARD to "keep up" with "everyone else". Others lie low and avoid holiday visits because they find them too draining. Others are somewhere in the middle.

Self-care is very important! LISTEN to your body. If your body gives you signs and symptoms that it's hurting or tired, perhaps you may wish to modify your plans to fit your body's capabilities. Be flexible. The world will not come to an end if you don't "make everyone happy". In fact, making "everyone" happy is quite impossible. You can't please everyone.

Be true to yourself. Know your limits. Know when to quit. What fun is overdoing over the holidays and then paying for it for weeks (or more) afterwards?

Learning how to pace yourself can be a challenge. Gain support for yourself from other patients with the same or related illnesses. This can be from face-to-face support groups, emails exchanged, phone calls, instant messaging/chat rooms, message boards, blogs like this, etc. Suffering in silence isn't healthy. If you reach out to find even one person who "gets it", it will be well worth the time/energy invested.

For those of you who are about to celebrate the holiday weekend in the U.S., try to implement strategies that encourage self-care. For those elsewhere around the world (and I notice from my live traffic map that this number is growing!), it doesn't take a holiday to cause people to display unrealistic expectations of chronically ill patients. Assert yourself when needed. Being polite but firm & honest about your limitations can make things easier (or harder) in the short run, depending on with whom you are interacting. Doing this almost always works out better in the long run, though.

Don't be afraid to say "no thank you... I can't make it" if an activity is beyond your limits. You can't please everyone.

Please have a happy and safe holiday weekend and find something (just about anything) that brings you joy and do it/use it). Don't feel guilty if you worry people will "judge you".

For those who are traveling, try not to overdo things and travel safely this holiday weekend.

Self-care is so crucial to managing chronic illneses.

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

6/28/2008

Deirdre's Brilliant Comment Has Resulted (Unknowingly) Into a Full-Blown Endometriosis Post!

Hi all!

An enlightened reader of our new endo blog wrote an inspired AND inspiring comment to my June 26 post "Endometriosis Patients Get Their Fair Share of Stress!"!!!

It was so inspiring to me that I was sure I'd run out of character space in the comments section. Soooo, my response to Deirdre's remarks is below. To read her short but very inspiring feedback/comment, see the the June 26th archive file for "Endometriosis Patients Get Their Fair Share of Stress!". Here is my response to Deirdre's post to the 6/26/08 article I posted. This is from 6/28/08 and is doubling as a fresh post by me for today:

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Hi Deirdre!

I’m glad you found us! Welcome to the new blog. :)

Thank you for mentioning the Center for Endometriosis Care located in Atlanta, Georgia. I do now remember seeing their website a few years back when I was very heavily into researching endometriosis on the Internet! I will have to pull up their site and refresh my memory! I do remember they had a helpful library section that I haven’t visited recently. I will definitely have to “take another look” at their site, now that you have reminded me about them! Maybe the library area I’m remembering and the educational articles you talked of are in the same part of the website? I can’t remember but I will definitely check it out. Thanks for the great idea for another helpful link! (If you page through my archives, you’ll find one of my earliest posts on this blog had a number of web links). This one wasn’t one of them; I had forgotten all about it. I’m glad you jogged my memory!

Yes, I have known about the OBGYN.com site for awhile.

See the link to it:

http://www.obgyn.net/.

You know some great resources)! :)

The 'http://forums.obgyn.net/endo/' section, in particular, focuses on ‘endometriosis in general’:

http://forums.obgyn.net/endo/.

As you mentioned, there is a cool forum available within that endo section. I remember posting back & forth on the OBGYN.net message boards years ago. I’m pretty sure that site is where I had gone through a phase of reading/posting tons of stuff on OBGYN.net (using the endometriosis message boards) over 10 years ago. (I remember the timeframe because I just celebrated my 10 year wedding anniversary and it was before that when I used to spend lots of Internet time searching for endo data).

Thanks for mentioning this too! I actually just pulled up the main starting page for www.obgyn.net and if you click on “select a topic” in the top right corner, a pull down menu appears.

In the http://www.obgyn.net/ pull down menu if you click on Endometriosis Zone, it will route you to ANOTHER cool website:

http://www.endometriosiszone.org/.

It's a neat site too.

Thank you for mentioning OBGYN.net!

I just stopped this mid-post to check my archives section… I wasn’t sure if I had listed OBGYN.net in early June (as intended) or not. I did not list www.obgyn.net in my June 2, 2008 article on endometriosis links: "Endometriosis and Endo-related Links You May Want to Check Out" but now our blog readers will know about it anyway thanks to you, Deirdre!

Thank you again for reminding me of how much awesome info is available over the Internet. When I was diagnosed in 1992, I didn’t even own a PC yet and if there was decent endo info available then by Internet (???) I’m sorry to say I sure wasn’t reading it!

I had gone to my local library in 1992 and they had NOTHING on endo. Not a word. The librarian even looked for me. No luck. (It was a very good library normally too). Times have changed.

It was in Barnes & Noble in the self-help book section that I found a listing in the very back of a women’s health book for the Endometriosis Association phone number: (1-414-355-2200). They now also have a website http at:

http://www.endometriosisassn.org/


This led me finding a local Endometriosis Association support group near me (the endo support group active in my area at that time). I was quite shy then (hard to believe, I know!!!) and quite nervous about calling a stranger to inquire about the endometriosis support group BUT I did it! (THANK GOODNESS)!!! My need and desire for support,help, and info overcame my fear of calling a stranger about my "endo story" and asking about the the endometriosis support group.

Through the local EA support group I was introduced to real live human beings besides me who had endo! IT WAS SO AWESOME TO TALK WITH PEOPLE WHO REALLY “GOT IT” !!!!!! It was absolutely refreshing and a huge relief to make that connection with others!!

IMAGINE: An entire room with women who had also been suffering in silence, like I did, UNTIL they reached out and found some of their fellow endo patients somehow! Our meetings didn’t have very many women but had PLENTY for effectively sharing engrossing “endo stories”!!!) I’ve learned that a support group of 2 can accomplish as much as one with 20. (I’ve been to meetings of both sizes). my friend Cathy taught me that "2 people makes a support group". She was right! I began my endo support group in August 2001 this is so very true!

As long as exchange of information is happening, it is ALWAYS worthwhile to network with fellow patients (of any illness) any way one can do so: in person is awesome if you can get it, phone works well too, email is outstanding, message boards & forums are super… Books are certainly a wonderful source too. No one loves books more than I do.

The thing is that when you interact with another patient BACK & FORTH and truly EXCHANGE ideas & info… it is a whole new level of support than simply reading a book without also having that more tangible connection. Comparing notes on doctors, treatments, success stories, losses, etc. really HELPS so many! I have learned SOOOOOOOOOO much about alternative medicine from my support group members that it's not even funny.

The beauty of blogging and giving feedback posts on endo blogs is that we can have an exchange while you are in the comfort of your own home even when you’d be too sick to find/make it to a support group meeting. I’m not saying anything can replace a support group meeting. However, blogging is increasingly becoming an important tool for reaching out to others for various reasons… including endo blogs.

It was in either 1992 or possibly 1993 (?) that I found my first endo support group. (I was diagnosed in 1992 after 10 years of not knowing WHAT I had)! For me… the rest is history! I started “surfing the Net” in 1995 and have been hooked since. I am really grateful to Endometriosis Association for the springboard of info I got from that organization in 1992.

So, again, thank you for reminding me about www.OBGYN.net because it is a well-known/reputable site in the endo community.

There are many endo patients who experience both endo and migraines. Many women in my current and past endo support groups have trouble with migraines. While I have no personal experience with migraines, I know from others that hormones can definitely be connected with migraines!

I have acupuncture treatments done regularly. While I personally have had acupuncture done for other medical reasons than migraines, I personally still do hand out “Traditional Chinese Medicine for Migraine” brochures (that I obtain from my acupuncturist’s waiting room area, with his permission, in short stacks at a time for giving to my endo support group). I’m not sure who the author/maker (?) of that brochure is and I can’t check now because I ran out of them. (I try not to completely ‘clean out’ my acupuncturists' waiting room brochures of ALL its brochures. So I do run out of brochures sometimes between our monthly endo meetings. Although it can be tempting at times to "hog them" because I take good care of my endo support group)! Ha ha.

Seriously, though, it may be a brochure affiliated with a product (Chinese herbs) or may not... I recall it being a brochure that was not specific to my acupuncturist’s office but was specific to migraines. I believe it was called “Traditional Chinese Medicine for Migraine”. If I remember to get more the next time I’m in I will try to remember to post the author/company that made the brochure but acupuncturists do treat migraines as a general rule of thumb. I distribute the brochures to my support group members at meetings since so many women have both endo and migraines!!

For women with endo (or anyone with migraines), acupuncture is certainly worth investigating! Please see my June 4, 2008 post Alternative Medicine Is Amazing! AND various YouTube acupuncture video clips (available right here on this blog!) if you (or anyone you know) is interested in learning about acupuncture. ACUPUNCTURE DOESN’T HURT! I CAN ATTEST TO THAT PERSONALLY! I even know of children who will attest to that. I delayed trying acupuncture for years over a fear of needles and now I wish I had tried it much sooner!

My licensed acupuncturist uses very thin Japanese-style needles. They DO NOT hurt and I am extremely sensitive (skin sensitivity and internally) compared to just about anyone I know. If I can do acupuncture with no problem whatsoever, I doubt if anyone out there would find it painful. I find it extremely relaxing. It even puts me to sleep sometimes!!! Acupuncture is MORE RELAXING THAN SLEEP to me. (I have sleep apnea and fibromyalgia and I really mean that quite literally!) I do not get restful sleep (except at acupuncture).

The YouTube clips cycle through on acupuncture, alternative medicine, endo, pelvic pain, infertility, laparoscopy, etc. The cycling of the clips is done by YouTube so you may have to be patient for the acupuncture clips to appear but when it is their turn to pop up, they will do so.

To view endometriosis-related YouTube video clips (including those on acupuncture) just see the “Pink Arrows to Open Slideshow. Random Videos will Cycle Through. Not responsible for content!” section in the right sidebar of my blog. If you look in the right (light pink background, medium pink text) sidebar, you’ll see what I mean. HINT: The videos occasionally collapse between cycles/groups of various topics. This is normal and when the videos are loaded they will re-appear on your monitor automatically. You don’t actually 'click' on the arrows as I originally thought to open the slideshow (I thought that clicking helped when I first created this blog but I’ve discovered that YouTube controls that part in their programming code for the slides).

Last but not least… I appreciate you sending the site of Dr. John R. Lee:

http://johnleemd.com/.

I had not heard of it before now and I did not yet have time to read through it BUT I did a quick peek at it -- just long enough to see that it looks interesting (and in line with the notion of alternative medicine options... i.e. things OTHER THAN just “drugs and surgery only" for treating endometriosis patients.

I am not a medical professional. I ask all readers of this blog to refer to the disclaimer at the very top of my homepage for this blog for more info on this.

Sorry about that interruption, Deirdre. Whenever I mention a site for a specific medical professional or treatment option I do my best to make it clear so my endo blog readers know that I don’t have personal experience with or knowledge of the person/treatment, etc. (in this case, I guess that would be Dr. Lee’s teachings, site, or any endorsed products)... I will look at his site about natural hormone balance, natural HRT, and bio-identical hormones. I will also ask my local endo group support group co-leader if she is familiar with Dr. Lee. (My endo group co-leader is a great resource for “natural hormone replacement therapy/HRT” vs. “traditional HRT” vs. “no HRT” at all and I’m sure she’ll find the site interesting too.

Finally, Deirdre… I would like to extend my sincere thanks to you… for stopping by and providing a number of interesting links and pieces of information! You gave me so much “fuel” with your brief comments that I am devoting this post to what we’ve discussed!!! Your references have inspired me to create this new post that will refer readers to that somewhat older related post on our 27-day-old blog. :)

Oops. I just realized this probably won’t fit into the comment board. I may very well make this the actual "Deirdre post" post itself!!!

THANK YOU SO MUCH for an outstanding comment/feedback post/actual post!! I most certainly hope that you re-visit our new blog SOON (and often!)… You are clearly very well-informed about resources (and on everything from websites & links… to hormones… to “migraines and how they are connected to endo patients”!)

You made my day with your posted comment! You have no idea how much I have enjoyed replying to your comment. Also, as I said… your comment has inspired me to make a (this?) brand new post and the posts will reference each other for even more to see/stumble upon in this vast world we call the Internet. We’ll catch more readers by posting in TWO spots on such important topics/links than just ONE!

THANKS, Deirdre!!! Enjoy the remainder of your weekend! :) (I need to learn how to program smiley faces the "right way" in these comment boxes. I use them a great deal)!

Deirdre's initial comments (before mine above) are also listed below in response to the article that I posted called "Endometriosis Patients Get Their Fair Share of Stress..."

Thanks again,

Jeanne

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From: deirdre [mailto:noreply-comment@blogger.com]
Sent: Saturday, June 28, 2008 4:47 PM
To: endendo@frontiernet.net
Subject: [Jeanne's Endo Blog] New comment on Endometriosis Patients Get Their Fair Share of Str....

deirdre has left a new comment on your post "Endometriosis Patients Get Their Fair Share of Str...":

For any women with endo who find your site, this is an amazing place - the Center for Endometriosis Care in Atlanta

centerforendo.com, also look under ''educational articles''

and a chat board

http://forums.obgyn.net/endo/ENDO.0806/date.html

also, the pill and other things can lead to low progesterone, which can cause migraines

check out johnleemd.com

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Posted by deirdre to Jeanne's Endo Blog at June 28, 2008 4:46 PM
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This article was posted by Jeanne via "Jeanne's Endo Blog" at www.endendoat.blogspot.com.

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