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Re: catamenial pneumothorax

From: anonymous@obgyn.net
Thu Apr 28 20:02:07 2005


Hi. I read abby's posting and am interested in communicating with her. I have had 2 lung collapses and similar treatment. my doctor also recommends lupron treatment and I have the same fears. I would like to know what did you ultimately decide to do and with what results. thanks.

At Wed, 7 Jul 2004, Mindy wrote: >
>May I ask you two, what symptoms you had prior to this
>occuring....meaning the location of pain. I am having endo pain under
>my right rib cage on my right side and it radiates up to my shoulder.
>When I breath, burp, hiccup, the sharp pain gets worse. It concerns me
>that the sharp pain worsens as I breathe in. I have had stage 4 endo
>removed and have had no pain where it was removed. Now three years
>later it's now this high up.
>
>Thank you,
>Mindy :-)
>
>At Tue, 6 Jul 2004, anonymous@obgyn.net wrote:
>>
>>At Thu, 13 Dec 2001, Giovanna wrote:
>>>
>>>Abby,
>>>Sorry (maybe I'm dumb)but I didn't understand what's the relation
>>>between your past problems and a probable endo.Is it ONLY because it all
>>>started on the day of your period?
>>>Do you have any endo symptoms?
>>>
>>>At Thu, 13 Dec 2001, Abby wrote:
>>>>
>>>>Hi! This is the first time I've posted. I'm 26 years old and have had
>>>>three collasped lungs in the past year. Two have required chest tubes,
>>>>I've had thoracoscopy and also chemical pleurisy. Even though all three
>>>>began on the day I started my period, some of my doctor's will not say
>>>>for sure that it's endometriosis. It's been a rough year. I'm very
>>>>interested in finding someone I can talk to who's lived through this.
>>>>Maybe even someone who's found treatment that worked! My doctor right
>>>>now want's to put me on Lupron, but I'm horrified by the stories I've
>>>>heard. It's nice to finally find people who at least know what this
>>>>is!!! I've love to hear from anybody, with any kind of experience. Thank
>>>>you so much.
>>
>>>>hi my name is daw and i have five children and have had cp since 1999. i have had a thoracostomy and talc poudage. since that i have suffered many more collapses and needed a total of 7 chest tubes. i have had hormone therapy that was unsuccessful and even caused more problems that i still deal with. because this is sooo rare it is hard to find qualified doctors to care for me. i live with much stress as a result of this!




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