Experiences with

Cystic fibrosis

HiI was diagnosed with bronchiectasis at the beginning of the year, at the time it was mentioned i have a mutated CFTR gene, which I assumed meant I was a carrier. My daughter had CF in the 80's. I've just been to the CF clinic, i thought it was for gene studies , and was gobsmacked to be told I have

55yr old man born with no immune system, Brutons XLA , led to bronchiectasis or Non Famillia Cystic Fibrosis. Lung conditions went into freefall since Xmas, now on oxygen 24hs a day and being referred for transplant list . Anyone out there either been or going through the same process.

Here are some examples: Genetic Disorders: Cystic fibrosis, Huntington's disease, Muscular dystrophy, Ehlers-Danlos syndrome, and Gaucher disease. Metabolic Disorders: Pompe disease, Maple syrup urine disease, Fabry disease, and Sickle cell anemia.

We had our egg retrieval in early July and have 3 viable embryos on ice following PGT-M and A testing (testing for cystic fibrosis and PGT-A done as standard as part of that). I am eligible for medicated or natural FET (which will be in October).

my husband has finally been diagnosed with unobstructive azoospermia due to being a carrier of the cystic fibrosis gene. I am not a carrier so we are looking at SSR. It’s £5000 for a micro tese privately - and we don’t have that money to spare currently.

Notably, hemin had no significant effect on intracellular calcium signaling and cystic fibrosis transmembrane conductance regulator (CFTR), a cyclic AMP (cAMP)-regulated chloride channel, and it showed a weak inhibitory effect on ANO2 at 3 μM, a concentration that completely inhibits ANO1.

the consultant mentioned my husband had a low sperm count /morphology & advised ICSI but asked my partner to have karyotping /cystic fibrosis blood tests done first, we're still waiting on these results since April as they said it would take 6-8 weeks.

so title explains itself. Day three post 5 day frozen embryo transfer. I am drinking more to help blood flow ect but it feels like I’m bursting for a wee very quicky after drinking and then there’s not a massive amount. It’s not burning but feel it could turn into that? If anyone has any other symptoms

I just met with my doctor after my 7th embryo transfer from donor eggs failed. Now I have 5 embryos remaining which she let me know are poor quality - two day 5 4CB embryos, a day 6 4BC and two day 6 4CC embryos. My doctor advised that I thaw and PGT test my embryos before doing another transfer

Hello, Hoping someone has been in the same boat as me and can offer some advice or reassurance. I had my egg collection on Monday and my estrogen levels were quite high. I was prescribed cabergoline prior to this and advised to take until after transfer. At transfer yesterday my doctor said my follicles

Hey, Day 11 post embryo transfer. 5 day blastocyst top quality 2 embryos. Sore breasts, headaches the last 5 days not much nausea. Been spotting brown discharge last two days. Tested day 10 and negative. Realised it's not till day 13 I'm meant to test. Anyone have any information? Please🙏

hi ladies Those of you who have taken this medication above in the subject line did you take it rectally or vaginally? I start taking this from Sunday twice a day plus the Lubion injection. The last time I had my fresh embryo transfer I was taking Cyclogest rectally, but this time I’m wondering if

I’m torturing myself & my clinic won’t give me any direction.. At my lining scan, lining looked great but they spotted a polyp right where they would have placed my embryo. They stopped my cycle, cancelled my transfer & advised I get the polyp removed. I’ve an appointment with a gynae surgeon on

hi ladies I hope everyone is well x So it’s time for 2nd embryo transfer, this time it’s FET, not fresh. I am on Progynova right now (which I was not on first time). Then I will start Cyclogest 2x a day, plus a progesterone injection daily. My scan is next week just to check all is fine before booking

I've found out this evening that my latest embryo transfer has failed. I've had 3 IUI and 3 rounds of IVF (one transfer each time) using donor sperm. I've got low AMH. I have one son from successful donor sperm IUI 3 years ago. I feel that I'm done with IVF now. I don't want to use donor eggs etc.

I’ve recently found out I have genital herpes and I’m due to have a FET in April. Has anyone else got HSV and doing IVF? Did you take an antiviral before the FET to reduce chances of an outbreak? Would they effect your response the the medication? Thank you!

hello, I'm just wondering if anyone has taken NAD injections before or during IVF? Any stories or thoughts please do share. I’m deciding if I should take it during my next round. Any advice is appreciated.

I’m waiting to have a fully medicated frozen embryo transfer and I’ve had to take norethisterone to induce a period as my cycle is so irregular. I came in to the clinic for a baseline scan on 30th Jan and all looked fine (no cysts) but nowhere near my period so they took bloods and gave me norethisterone

To cut an extremely long story short. I'm 50, have had painful periods my whole life. The past 3 years the symptoms have been much worse, with constant pelvic pain with associated bladder and bowel issues.I had a hysterectomy a year ago for Adenomyosis and multiple Fibroids. All of my tests for Endo

HI All, I have PCOS (was very severe but not seems to have reversed with meds, diet and exercise!) and went through IVF. I had 2 failed transfers and am currently prepping for FET no3. As I appear no longer polycysic, my medical team suggested trying Letrozole to build uterine lining which worked