Recurrent Miscarriage Thread

Thank you Mandy that's really kind of you to even consider wishing me luck after what your going through, but I really appreciate it, also someone understanding, I feel like today is my angels day an she sent me another baby so i still haven't told him! Maybe tomorrow! Thanks for all your hope and support ladies xx

I wish you all the best with this pregnancy. I believe your angel did send you this precious gift :hugs::hugs: You give me some hope in TTC again. I lost my Ava at 18 weeks in March and all I want to do and be is pregnant again.
That is why i come to read this thread, it gives me hope, something I really need now..
XOXOOOX :hugs::hugs::hugs:
 
Hi andypandi that must be so hard i have had all first tri losses an thats bad enough so sorry for your loss. We do amaze ourselves what we deal with, as far as getting pg i had to take clomid every pregnancy but it really is a wonder drug for me! It gets me pregnant, I also read this thread an unfortunately there is always sadness but lots of joy to! Wonder drugs that actually work etc an it gives us all hope we will one day get our forever baby. I used a clear blue fertility monitor to i think that helped definately pinpoint ov! Good luck and thanks again xx
 
having a really bad day!!!

Just want this to be over with already. I had a termination due to severe kidney failure and had a kidney removed. and now 2 weeks and 1 day later, I am still bleeding.

this on top of the huge amount of miscarriages I have had, I Just bloody done know what I did to deserve all this???
It is one of those days where you just wonderif you will ever ever have happiness again.
 
Sorry to hear that 9babies!! Do they know the cause of the kidney failure? Have you ever had an HSG or MRI to check for uterine abnormalities? I know mullerian abnormalities (reproductive tract) have been shown to be associated with kidney issues. May be worth looking into if you haven't already with the large number of losses that you have had. May explain some things? :hugs:
 
having a really bad day!!!

Just want this to be over with already. I had a termination due to severe kidney failure and had a kidney removed. and now 2 weeks and 1 day later, I am still bleeding.

this on top of the huge amount of miscarriages I have had, I Just bloody done know what I did to deserve all this???
It is one of those days where you just wonderif you will ever ever have happiness again.

I am SOOO so so sorry :( :hugs::hugs::hugs::hugs::hugs: I know nothing anyone can say can ease the pain you are going through - just know that we are here to lean on and talk to if needed..:hugs::hugs::hugs:
 
yeah my lupus caused the kidney failure!!! It probably didnt help that doctors didnt think I had lupus for years evne though I told them I think I have it, and by the time they found out this year, I was having organ problems.

I am just so dang sad. and I want to be pregnant so so bad!! but it wont happen bc I am still bleeding.
 
Hi everyone, I have just been to my recurrent miscarriage clinic appointment. I had 10 vials of blood taken. They said they are going to run full checks on everything , but initially said not progesterone. This is what I believe to be my problem so they eventually agreed to check that aswell. I've been told its going to take 6-8 weeks for results to come back, is this normal for the NHS?
I was quite surprised at this, but maybe Im just impatient.
Only then when the results are back will I see some kind of specialist to discuss the results and an action plan put in place. Only then will I also see a consultant about my uterus anomaly..double uterus! The nurse I seen today knows nothing about this. I feel quite positive that we're moving steps in the right direction but I really thought I'd see a consultant sooner about my uterus and also my one kidney that they have discovered noone seems bothered at all about that. Not sure what to think
 
hey hun, 6-8 weeks is the general wait time im afraid (where i had my tests done we had to have some reapeated after 6 weeks and then had to wait a futher 6 weeks and get the whole lot of results together) im not sure ur kidney would effect u with reagrds to pregnancy, i think the general thing is these places are so busy so they like to review everything (scans, blood results etc) all at once. hoping you get and answer and solutions soon hun xx
 
That is a long time but I think some of those bloods need to be sent here in the states so that may add to the delay. Here in the states most results come back within 2-3 weeks.

Hang in there, your case sounds pretty unique and they may need more time to come up with a game plan.
 
9babies :hugs: I think we all have those days. You didn't do anything to deserve this. I often feel the same way, but I truly believe we just got handed a bad deck of cards.

Wow, I can't believe it takes 6-8 weeks with NHS! When I was having all of my testing, I had 17 vials taken and all the results were back in less than a week. I hope they get to the bottom of it and it is easily corrected Justkeeptryin.
 
Tina, I think we've all experienced people who have said the wrong thing. No matter how kind a person is, if they haven't experienced a miscarriage, they often say the wrong thing. What really bothers me is how quickly people expect you to recover from it. I've never received a card or anything after my losses. You send cards when people die. I don't know how this is any different. You asked about PPD. I agree that it can be part of the process. I also believe that long term PTSD is part of the process, especially if you've had recurrent mcs. I find myself getting triggered all the time. I read the formal description of PTSD and it fits me pretty well.

You know what's interesting is that with my most recent loss last week (my 4th), it was ectopic and I had surgery. I've had more people reach out to me about this loss than any other. And quite honestly, this one was the least meaningful to me because I knew it was doomed from the start. With my first loss, I made it to 10 weeks and had a heartbeat. I'm still not over that one, but I didn't get nearly as much attention. I think people can relate to surgery, but can't relate to miscarriage.

I'm making it my mission to educate people. I'm tired of hitting the ignore button. If people say something wrong, I let them know. I just don't care about sparing other people's feelings at the expense of my own anymore. I'm so sorry you had to endure stupid people saying stupid things. You don't deserve it. xoxo
 
Tina, I think we've all experienced people who have said the wrong thing. No matter how kind a person is, if they haven't experienced a miscarriage, they often say the wrong thing. What really bothers me is how quickly people expect you to recover from it. I've never received a card or anything after my losses. You send cards when people die. I don't know how this is any different. You asked about PPD. I agree that it can be part of the process. I also believe that long term PTSD is part of the process, especially if you've had recurrent mcs. I find myself getting triggered all the time. I read the formal description of PTSD and it fits me pretty well.

You know what's interesting is that with my most recent loss last week (my 4th), it was ectopic and I had surgery. I've had more people reach out to me about this loss than any other. And quite honestly, this one was the least meaningful to me because I knew it was doomed from the start. With my first loss, I made it to 10 weeks and had a heartbeat. I'm still not over that one, but I didn't get nearly as much attention. I think people can relate to surgery, but can't relate to miscarriage.

I'm making it my mission to educate people. I'm tired of hitting the ignore button. If people say something wrong, I let them know. I just don't care about sparing other people's feelings at the expense of my own anymore. I'm so sorry you had to endure stupid people saying stupid things. You don't deserve it. xoxo

You are so right and thank you so much!! :hugs: this means so much to me.. :( what's sad about that person is that she DID have a miscarriage, but since I said I was doing ok with it (at the time), she thought I didn't care, and in the end called me a fake, a liar and an attention seeker - and also selfish. I too knew this one was going to not go well from early on. I was more devastated the first time - at 8 weeks we found out the heartbeat had stopped at 7 weeks, (we had seen it at 6 weeks). I was a - well - I can't describe it. It was devastating - I am sure all here can relate. I had a D&C the day we had scheduled to celebrate our 12th anniversary. We checked into our cabin we had reserved that night after the D&C. It was - horrible. I tried to use that little get away to heal a bit, but 2 days at a cabin wasn't even close to what I needed.

It got worse, and i won't go into the gory details here - but I ended up quitting my job due to a cruel person that I worked with who told me she had been with people to have AB******S - seen the heartbeat - and it didn't mean a thing.

This time around, I knew what to expect (sort of), so when the HCG's didn't climb, which is what happened before, I wasn't caught of guard. We never had a Ultrasound, my HCG didn't get over 200, and I started bleeding. I was depressed, sad, and heart broken, but mentally dealing OK. Initially - I'm learning it takes a few days before the grief really kicks in - that's me anyhow, it wasn't instantaneous. I try to remain in control of my emotions. Anyhow - because I didn't totally break down as soon as I found out, someone thought I was blowing it off and didn't care. And when i tried to explain myself, I was accused of - well what i mentioned above.

I feel sorry for the person - they don't understand how I was trying to cope, they've had one miscarriage, not many (thankfully for her), so she can't truly understand.

It all was very painful and I feel some comfort here because I can post this in a location where we have all had more than one loss, and maybe find people who understand that each time may not be exactly the same, and, yes, maybe we are better prepared the second - or maybe third or fourth time - maybe we are more numb. I think - the further you are along, the more devastating it is. So, I was farther along the last time, and felt the worst of it, this time I was less along, so had already had WORSE, so was better handling it. If I had been farther this time, it would have been more devastating. I don't know - maybe i'm trying to rationalize too much.

:cry::cry::cry: reading your post, it just feels so spot-on....

Thank you so so so much!
 
hi ladies,

Sorry for interupting a thread but just want to tell my story.I relied on b and b so much last year after 3 missed miscarriages, each time not having news confirmed till the scan at around 10-12 weeks. I too had little support from family who thought i was 'maudlin' over the miscarriages and would dismiss me with things like its very common and its just one of those things. 3 months after last miscarriage i fell pregnant again. Consultant put me on progesterone pessaries 6-12wk , clexane injections and low dose aspirin up to about 26 wk. My healthy little baby boy was born in May!Btw all tests done showed everything was normal and no reason for miscarriages. I hope you all get some good news soon xx
 
poisonwood our storys are very similar!! i had 5mc's all unexplained nothing every came back from testing etc, did the progestrone pessaries til 12 week on baby asprin currently (should stop at 36 weeks) and am now 25 weeks gone with a perfectly healthy little boy! :) xxx
 
What great stories you two have. Mine is similar too. I had 3 mcs. Got pregnant 1 month after the 3rd mc, doc put me on progesterone and I put myself on the baby asprin. Stopped prog. at around 14 weeks and can't remember when I stopped asprin. The end result was a beautiful, healthy boy born at 37 weeks. So we may be onto something!
 
hi ladies, i havent been on here for a while but I just had my third mc last week. All 3 have been the same, I get a positive test and start spotting 2 days after getting it. I have loat all hope that I will every have a little one. Thanks for letting me share.
 
All of the above stories here give me hope. I just really hope that Im given progesterone supplements either way to support my next pregancy. There is too much evidence out there that it does work.
At my miscarriage clinic I got the impression from the nurse that she's not convinced about progesterone, she said there is still so much research going on into it. I dont know whether its better for my results to show something thats wrong so it can be treated or better to come back normal
 
It seems there are people in the medical profession who are not convinced about things that may help such as progesterone/aspirin/heparin/prednisolone. My consultant has prescribed me all of the above in the past but hammered it home to me that it was all empirical and that there was no guarantee. I accepted that but have been eternally grateful to be under his care. He's a very progressive man who believes anything is worth a shot but at the same time doesn't believe in giving false hope.

He summed it up to me when I saw him after the last scan which showed no growth of the sac and that I would soon be miscarrying. He told me that fifteen years ago they had no idea that clotting disorders could cause pregnancy problems and who knows what the next fifteen years will bring in medical knowledge :)
 
hi,
im sorry to hear about ur losses.. i am just curious, which tests have you had? and are they your first blood test or with a consultant?
the reason i ask is because after my 3rd m/c me and my partner had some blood test, and after suffering another m/c this year, i have been refarred to a consultant on aug1st, and i cant imagine what they are goin to look for or do?
 

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