Hi ladies and welcome Lucaswood, you're in good company here and will get loads of support. I'm 38 and a long history short I had 3MCs then my DS in November 2010, and then another 3MCs, all this year and the latest one was only last week

. As we're all in the 35+ bracket it is bringing with it the added difficulties and complications and I am currently getting investigated AGAIN, which you can read about below. Looking forward to getting to know you
Twotogo... glad to hear you are doing better this morning
Coy... what a gorgeous baby bump, I'm so green lol and wish it was me. You are looking fab honey and all this activity will mean you are so fit for labout, it'll be a breeze
Jess... how's the training going?
Babywhisperer and Terri... how are you ladies? Babywhisperer I read a post earlier but cant remember it and I was going to comment

. I'll look back this evening when I've got time to read properly

.
Sorry to anybody I've missed, I'm still in work so it's a quick catch up for now.
Happy Friday Everyone!
Angel - any more news from your DR? How are you doing? Big hug
Now Ali, I really couldn't forget about you


. I've been avidly reading snippets when I can this week to keep up with your progress. I'm glad things went well and sorry you probably have already posted this, but what happened the other eggs that they can't freeze them? I'll read back later this evening (GMT

). I hope you are taking it easy my lady?

Can't wait till next week when you test, this surely has to be your BFP!!!!
Well, here is my novel from my appointment at RMC yesterday. A mixed bag to be honest...
Upon arriving at 08.35 yesterday morning and making small chat to the nurse she showed me into a room with what looked like a bed and scanner etc. I didnt realise the senior consultant was already in there and I panicked and said that there was no point scanning me as I had another MC last week. She was very apologetic and introduced me to Dr Hunter (the highly recommended RMC I was meant to see a fortnight ago).
Well basically I got a gruntled hello and that was it. No sorry to hear that, no how are you, no are you still bleeding, any fever etc looking for signs of retained products. Nothing. So that got my back up a bit already
He went through my basic history, how many MCs, age and sex of my only child. In fairness as this is a new hospital I am under they do not have my years of notes from my 15+ years of gynae problems and procedures but he didnt even seem interested in obtaining them.
Long story short after a somewhat strained 20 minute meeting:
- Metformin for PCOS - NO, not thought necessary as I can conceive
(but it is meant to help prevent MCs for those with PCOS as well so I'm pissed at this comment)
- NK Cell testing - I asked his opinion and if he thought it would be necessary/useful. He banged on about different schools of thought and Prof Quenby in England etc and that if I wanted to look into it Google it. They could do the procedure at the Royal and then send the biopsy to Prof Quenby or I can organise a private consultation with Prof Quenby. Either way it's up to me to look into it and decide what to do

. He didnt mention if the procedure could be done under the NHS and then a small fee to Quenby or a full private fee 
- Progesterone - slight possibility of putting it in protocol as I'm in the 35+ bracket. I told him I knew the research

- Ages - he sighed and commented 'getting old' when I told him my DH's age which is 43

. He then mentioned the current trial going on (name I cant remember) researching sperm quality and age and to look into it and decide if we want to try it
. Like HELLO, how is this helping??? Give me the contact details at least

The better news;
- We (DH and I) are at last getting chromosome testing done next week at consultants request, which my GP (female) has helped me sort as DH is in a different practice to mine.
- Consultant wants to do a hysteroscopy which I dont think I've ever had done to check the shape of my womb etc. I have had a laparoscomy so I thought that information could have been confirmed then?
I can only remember from that I have an introverted uterus and hostile womb, i dont remember anything being mentioned about abnormalities with the shape etc. Can your womb shape change as that was done about 10 years ago?
- I had to choose to be in the 'pool of consultants in the Royal' or be dedicated to Dr Hunter. In my madness I have chosen to stay with Dr Hunter as he is meant to be the best here, was highly recommended by my GP and to be honest I am tired of having no consistency as I have to repeat my history at every appointment to a different consultant, who again may have a different view of treatment. The downside is his waiting list is a bit longer, it may take about 2 months to get the hysteroscomy but he said at that appointment we will discuss and decide a plan of care. So I am going to have to just be patient and WTT for a couple of months
. It makes sense we all know but yeah is pants 
.
Dr Hunter's protocol appears to be aspirin, high dose folic acid, claxane from BFP, and possibly progesterone which I will push for as I am in the bloody over 35+ bracket. He does have about an 80% success rate so I just have to keep reminding myself of this

. I'll look into the metformin more, perhaps my GP will give it to me or send me to endo.
I also took the bull by the horns at lunchtime and rang Dr Quenby's office at Coventry to get some advice. The secretary was a little bemused after I explained the outline I had been given regarding the NK Cell testing but we came to the conclusion Prof Quenby and Dr Hunter must have done this in the past so the secretary is going to talk to Prof Quneby about the 2 options (procedure at Royal or private consultation) and she will get back to me. I also fly frequently to Birmingham with work for meetings so I'm going to say if it is better to just get the testing done there we will try to schedule it in over the next couple of months

. It'll cost £360 though to get it done private and with my DH on a 3-day week this may be an issue but I'll cross that bridge if we come to it (the joy of credit cards


)
So phew, after that ramble I'm not really any further forward, a bit pissed but also trying to be positive that things are happening a bit and hopefully I'll get a care plan in place before the end of the year.
But if I am being open, I really do have this niggly feeling that the powers that be are trying to tell me something, hurdle after hurdle, is it ever going to end? Maybe I should just be realistic and be thankful I have one DS and give up on all this...