Pulmonary Embolism Support Group
By far the most common form of pulmonary embolism is a thromboembolism, which occurs when a blood clot, generally a venous thrombus, becomes dislodged from its site of formation and embolizes to the arterial blood supply of one of the lungs. Symptoms may include difficulty breathing, pain during breathing, and more rarely circulatory instability and death.
Rachael81
Hello everybody
I have been away from a long time and its good to be back
Most of the time i try to pretend i have a normal life, but I am tired to fool myself, my li
fke hasn't never been the same and its depressing
So, my last visit to the hematologist she said that I do have 2 mutations and I kind of Lupus in my blood, and that I will need to take xarelto forever. my PE was in may 2013.
She said I can not have kids and that I could die if I try, my husband got really scared and did a vasectomy.
She also asked me to cancel my plains to do a plastic surgery (breasts) and said this is not safe at all
So now, I am at age of 35 wondering if this it, I am just a sick woman incapable to be a mother, and this hurt me so much I spend mostly of my days wondering why this is happening to me, while my whole family and friends are having babies ( they do not know I am sick or a I had a PE)
I just felt the doctor were very cold about that and didn't care about me, and I am always wondering if maybe there was a treatment or something.
(she told me I could take lovenox during pregnancy but its still high risk)
I have been in 3 hematologist, and I kinda gave up to find a better one.
I am sorry for venting, I just feel less woman than everybody else after that, and i wonder how to get rid of the "this is not fair" feeling,
We are thinking about adoption later, but I don't want to rush and do it just to fix something
has anyone else going through this?
I have been away from a long time and its good to be back
Most of the time i try to pretend i have a normal life, but I am tired to fool myself, my li
fke hasn't never been the same and its depressing
So, my last visit to the hematologist she said that I do have 2 mutations and I kind of Lupus in my blood, and that I will need to take xarelto forever. my PE was in may 2013.
She said I can not have kids and that I could die if I try, my husband got really scared and did a vasectomy.
She also asked me to cancel my plains to do a plastic surgery (breasts) and said this is not safe at all
So now, I am at age of 35 wondering if this it, I am just a sick woman incapable to be a mother, and this hurt me so much I spend mostly of my days wondering why this is happening to me, while my whole family and friends are having babies ( they do not know I am sick or a I had a PE)
I just felt the doctor were very cold about that and didn't care about me, and I am always wondering if maybe there was a treatment or something.
(she told me I could take lovenox during pregnancy but its still high risk)
I have been in 3 hematologist, and I kinda gave up to find a better one.
I am sorry for venting, I just feel less woman than everybody else after that, and i wonder how to get rid of the "this is not fair" feeling,
We are thinking about adoption later, but I don't want to rush and do it just to fix something
has anyone else going through this?
Posts You May Be Interested In
-
Look at what my best friend did with my picture!
-
We all have 24 hours in a day. How we spend these hours is important. Watching a little bit of a video about how sitting affects us made me aware of how much sitting and laying down I do. Gonna have to work on that.Your turn. Tell me another truth.
I'm sorry you're going through this difficult time. I was pregnant with my second child when I had my PE and finished the pregnancy on blood thinners. I'm now pregnant with my 3rd and on blood thinners again. My situation is not the same as yours, so I'm not sure how much help I can be. For example, I don't take blood thinners when I'm not pregnant. I have Factor V Leiden but not any other mutation or lupus as you mentioned. One thing I might suggest is getting a second or even third opinion. My hematologist was supportive of us having another baby, but my obstetrician was a lot more cautious and not very supportive. I also consulted with a third doctor before making a decision about having a third child. My obstetrician considers me a high risk pregnancy but everything has gone very smoothly so far. The hematologist told me being on blood thinners this time around is a lot different from being on them the last time when I had several clots in my body. The dose was a lot higher then, now I'm on a lower preventative dose of blood thinners just to reduce the risk of a clot. I went on blood thinners as soon as I found out I was pregnant. I feel confident everything will be OK and I'm followed closely by my hematologist and obstetrician. But like I said, it doesn't sound like we have the same situation. Perhaps to put your mind at ease or give you some closure you could consult another hematologist who has experience following women in pregnancy. It's a big decision to make based on one doctor's opinion, so maybe one or two other opinions may help. Good luck.
One thing I am curious about. You mentioned lupus. Do you have lupus anticoagulant or lupus the autoimmune disease, because they're different and I'm not sure if by being "a sick woman" you mean that you are suffering from lupus the autoimmune disease.
Can I be honest? If you feel like you're pretending to have a normal life, comparing yourself to other women and feeling less than female, something is amiss, ok? I'd turn your focus to making peace with your body and your circumstances, and whatever may or may not happen in terms of children. I would really work on trying to not compare yourself to other women and to focus on you and your mental, physical and emotional well being. I don't have children but I never feel less than anything, certainly not less a woman, because I don't have kids. Do you think your husband feels less a man because he had a procedure that prevents release of his sperm when he ejaculates? Probably not. Do you look at other women who are infertile or can't carry a baby, or even choose to not have children and think, those aren't full-fledged women? Probably not (god, I hope not). So why on earth would you choose to see yourself that way? That kind of thinking is like poison.
Maybe seeing a therapist could help you sort through your feelings and help you reconcile some of this stuff. It's very hard when the unexpected happens in our lives and all that we planned comes tumbling down, I know. All you can do is adjust your plans and keep moving forward. That's all anyone can do when life throws them a curve ball.
Sorry for the delay, I was with no internet.
i want to thank you both so much for the words, I really appreciate and I was in much need of that.
I believe before jump to adoption or any kids relate treatment I need to make sure I don't see myself less woman because of my disease and go from there.
having kids won't make up for the hole in my soul, and I am stronger everyday
I have the lupus anticoagulant, and I don't know much about this yet, I have been in 2 doctors and they basically told me to don't worry about it
Thank you again