Category: IVF Meds

FET #6 Lining Check

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Just a quick update about this FET #6.

I started taking Tamoxifen on 2/2. I took it, once a day for 5 days. On 2/6, I also applied 2 estradiol patches.

And the results today…..nothing.

My lining is non-existent(1mm and with fluid) BUT my follicles are not growing either…weird. Last time, I had 2 follicles around 20mm. That should have produced enough estrogen to grow my lining but it didn’t…only got to 5.1mm.

So we wait. I am to stop the estradiol patches and see if my body will wake up and produce some estrogen on it’s own.

And that’s the update….not exciting but I go back in on Friday to see if anything is going on.

I’ve had my frozen embryos since Nov.2013 and Jan.2014.

And I’ve never had a transfer.

I understand when women get sad, or frustrated when they can’t transfer their embryos in their fresh cycle and have to wait another month for an FET….but over a year?

It’s just not right.

When I go to my RE’s office, I think about them. How long they’ve been frozen there….just waiting too.

Makes me sad when I think too much about it.

But what can I do?

Keep waiting…and praying…gonna do a little more praying.

I just don’t know what else to do.

FET #4: Screw Estrogen

O.k….so after having a short 23 day cycle last month….I began FET#4…

So far I’ve been through 3 other FET’s to try to build my lining to an appropriate thickness to carry a pregnancy….it’s only ever gotten to 4mm……every….single….time….

I’ve used Oral Estradiol Estrace (of doses up to 8mg-10mg a day), Vaginal Estrogen suppositories(3mg a day), Viagra, Trental 400mg, Vitamin E 1000mg, Wobenzyme, acupuncture(for the past 2 yrs), I even went to a Chinese Healer…yes…he was on “Ripley’s Believe It or Not” show as able to heal the “unhealable”…I know…I sound desperate…..

and I am….

I’ve had these 6 blastocysts waiting to be transferred since Jan(and one little morula from my first IVF in Nov)….just sitting there…frozen….waiting for a home…..and I’m really trying to give them one…..

So we are here….

2 weeks ago, I started Estradiol Valerate(Delestrogen) shots. They use the same needle size as Progesterone shots. They look like GIANTS compared to the tiny IVF med shots…here’s a pic:

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But once again….no reason to freak myself out….we TRULY are stronger than we think….and they are not that bad…you just have to make sure you ice that area…and it’s really numb…, pinch your skin pretty tight…and don’t put the needle in too fast…steady and when I’m pinching my skin I poke my finger nail into my skin too…so I can’t really feel the needle or meds….just a little advice 🙂

Lining checks: Not good 🙁 There is still fluid in my lining and it’s only about 3.6mm…..boo…hoo…also, my E2 is at: 4108…too high….so I’ll lower my dosage of Estradiol Valerate and only 2 Estrogen suppositories instead of 3 per day.

So, to me, obviously estrogen does not work on me….too much, too little…I get the same poor results….thin lining.

I’ve realized I have to be my own scientist. I read all of the literature. All of the studies. ALL OF THEM.

Now that I know estrogen is not going to cut it for me…next month we are trying a drug called Tamoxifen to grow my lining.

It works a little differently than estrogen…it binds differently to certain estrogen receptors….and has shown promise for women with chronically thin lining.

Who knows if it will work….but I’ve gotta try right? I’m not giving up on myself yet.

Obviously, my RE continues to suggest a Gestational Carrier for me. He feels that, that is the only way I’m going to be able to have my own child. He believes that my endometrium has been severly damaged due to my appendix rupturing, causing chronic infection and inflammtion throughout my body. He says that looking into a gestational carrier now would be no harm starting the process because it takes a while and he knows that I still want to try to grow my lining…

What he doesn’t know is that I WILL carry my own baby. Period.

I will not give up on myself. I will not stop researching studies and various techniques throughout the world for women with my problem. There HAS to be a solution. Some link. Some medicine. Some sort of indirect association that just needs to be found to put it all together.

I’m not only doing this for myself….I refuse to give up on the hundreds of other women with this problem, Chronically Thin Endometrium. If they don’t have the strength or opportunity to search and test other options before having to turn to a gestational carrier…I will do the work for them. I will fight for them and I will post everything here.

I didn’t go to med school. I’m not a Dr. or an RE….and I never will be. But I am a patient…and I have a problem….and that problem needs a solution. I understand that certain treatments that “should” work are not working….so maybe we should think out of the box? Obviously my case is unique….therefore I need a UNIQUE plan….seems simple right?!

I am very thankful that my RE has agreed to try “experimental” protocols with me(let’s just say I wouldn’t take no for an answer…ha!). Don’t get me wrong, I don’t want to put my life in danger but I also don’t want to give up on something that I feel can be solved, can be figured out…with a little effort….

So, there ya have it. I will continue these Estradiol Valerate shots for the next week (maybe my lining will miraculously perk up??) and then on to Tamoxifen. It is one of those experimental things….it’s currently used for breast cancer patients but this study showed promising results….for us thin lining ladies….

Don’t give up on hope. Whether it be for thin lining, PCOS, poor egg quality, immune issues, overweight, underweight, no ovulation, RPL, etc…..you are not alone. Remember…there’s always someone in your corner….cheering you on..and fighting for you….

Determination…..that’s what it’s about and I’m ready to battle….

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