 |
 |
 |
|
|
|||
|
|
||||
|
||||
Re: ENDOMETRIOSIS: Is LUPRON safe to use as treatmentFrom: Melanie M. (anonymous@obgyn.net)Thu, 21 Jun 2007 17:39:14 -0500 (CDT)
Hi ladies, this is my first visit to this website and I would like to share with you my experience. I am knocking on 35, had 2 laparoscopies, and 1 failed IVF. My dr recommended after my 1st lap. to get on Lupron. After much research, reading and discussion with my family, I opted against it. The biggest reason why is because endometriosis is a disease, there is currently no cure. After you finish with your Lupron shots and deal with all of the side effects, you may find a reprieve from all of the endo pain, etc but it will grow again. I will tell you that for years, I carried economy size bottles of tylenol and ibuprofen and this STILL did not take away the painful periods I had. I have given up on the "traditional" treatments of medicine that most doctors will refer you to. (sorry, not knocking any doctors here, this is just what has worked best for me) About 4 months ago, I began working with a nutritionist that specializes in endometriosis and infertility. Being extremely skeptical about it working, I gave it a shot anyhow because after all this time, nothing else has worked for me to get rid of the pain. I am SO happy to tell you that I now have nearly zero pain from endometriosis. I have not taken any pain meds for 2.5 months, I have energy and feel healthier than before. How great it is to be able to make plans during my cycle time and know that I will actually feel like doing something other than lay in bed. It really seems too easy to say that a diet change and nutritional supplements could be your answer. Maybe this is why it took so long for me to figure it out!! Remember, this is your body and your life. No one has to bare the pain or side effects like you will. It is ok to question your doctor's advice. You must be an advocate for yourself. I know you are probably still in shock from the diagnosis of endo, but I promise, you are not alone. There are thousands of women out there, support groups,and tons of information that will help you. Here are a few resources that might be of help. The nutritionist I would recommend is Dian Shepperson Mills, website is http://www.endometriosis.co.uk. I would suggest joining the Endometriosis Association, they have a very informative monthly newsletter, website is http://www.endometriosisassn.org. I hope that this is useful for you.
|
|
Return to ![[ Women's Health Forum ]](http://www.obgyn.net/images_women/wh-forum.gif)
Report TECHNICAL Problems ONLY to: webmaster@obgyn.net
Last Updated: Sun Nov 2 06:34:31 2008