Dear Earthpower9 & Bella - welcome to the thread. I only found Dr Matthias thanks to a gorgeous woman I met at a Genea Support Group - so I feel it was meant to be as well. At least now I will know that I have really tried everything.
Just in terms of telling your doctor: I elected to swap FS to Dr Geoffrey Reid at Genea as he was recommended as being so much more open to immune therapy than my own FS at Genea. I am so glad that I did this as my husband is much more comfortable having all of the doctors in the loop. That said, you don't need to tell Dr Sacks - the last thing that you need to have is a negative doctor frightening you when he hasn't been able to help.
I did have to have an endometrial bioposy (at Hurstville Private). Dr M uses his own pathologist so gets the results that he wants. The blood goes to Chicago - they took 16 vials from me and 4 from my husband - as the clinic in the US is very advanced and can do the types of testing that you cannot get here. All good. I am 3 days into my 21 days of prednisolone prior to my stimulated cycle. Finally I feel like I am getting the treatment that I need rather than doctors just 'trying' something for unexplained miscarriage and implantation failure.
Nat84u - you lucky girl not having to do IVF this time. Good on you! Unfortunately, I will be having the whole kit and caboodle - clexane, prednisolone, IViG (at some vast cost!) and a whole lot of hope. M
Just hope that I get an embryo now that I have everything else all lined up.
Please let me know how everyone gets on. Sending warm wishes to you all.