Hi im Lauren

[Lauren]

I really would love to speak w someone else about ppcm...I haven't ever met or spoken w anyone who knows what i feel like. Please feel free to email me anytime. OLENAMAC1@aol.com thank you :)

[tabs]

Lauren, All of us here have PPCM. Please join in our conversations. What would you like to talk about? How long has it been since your diagnosis? How are you doing now?

Twilah

[mikeyandBellesmommy]

Lauren welcome, all of us here have/had or have a family who has or had PPCM. We are all here for you and I am SURE we all can answer any questions you may have..

Read through the boards and tons of your questions will probably already be answered LOL!

Please feel free to e mail me anytime if you need to talk

CMarino@centercapitalcorp.com

[Karen T]

Hi Lauren
I'm Karen and also live in NH (Nashua). I have a soon to be 12 year old, 10 yr old and 3 yr old (my PPCM Baby). Sounds like you have been through so much! Please feel free to email me @ KThomasRN@comcast.net
Keep in touch!
Karen

[Lisa V]

Hi Lauren,
I would like to send you a WELCOME to this wonderful board of amazing woman. We are here for one another to listen, give advice and lend a shoulder too. I was diagnosed 5 years ago this month with an EF of 10% and I am currently holding around 50% now. I have been active on these boards since diagnosis and I have found them to be helpful and inspirational as well. I hope to see you around alot.

[dawn]

Hey Lauren! Glad you found us!

My bio is posted. Quickie: Diagnosed 7 days post partum, EF 15-20%, pulmonary emboli, lots of meds, fully recovered one year later. I'm 4.5 years past diagnosis.

Hope you find some friendship and support here.

dawn

[Special K]

Hi,

Welcome to the site. There are a lot of women here that understand what you are experiencing. It has been a great help to me knowing that I am not alone. I hope you find the same comfort from this site. :D