Ce maturoi :) Acum s-a inventat aspiratorul :))))
E bio:)))
Postat 10 august 2016 - 15:20
Ce maturoi :) Acum s-a inventat aspiratorul :))))
E bio:)))
Postat 10 august 2016 - 15:25
E bio:)))
Corect
Postat 10 august 2016 - 18:17
Buna,
Caut pe net in lung si in lat ce sa mai fac... si va rog si pe voi sa va dati cu parerea referitor la niste articole gasite azi:
http://natural-ferti...ampaign=NFI-Ads
http://natural-ferti...ing-a-baby.html
http://natural-ferti...-fertility.html
http://natural-ferti...y-wobenzym.html
As mai face ceva pe langa FIV, ca dupa ultimul FIV (cu ovulatie inainte de punctie) FSH-ul meu a devenit 35... astept sa vad daca si luna viitoare va fi tot asa, sau a fost doar o luna proasta (niciodata nu l-am avut atat de mare, insa acum am doar 1.5 luni de cand am luat cele 53 de fiole cu Menopur... poate a fost influenta de acolo).
Voi ce mai faceti ca tratamente alternative?
Multumesc.
Editat de laura_71, 10 august 2016 - 20:52 .
Postat 10 august 2016 - 18:28
Eu am facut/fac tratamente la Sovata (irigatii cu apa sarata din lacul Ursu + tampoane cu namol si impachetari cu namol din acelasi lac). Medicul de aici a vrut sa imi recomande Maca si Vitex, insa, dupa ce i-am spus ca iau zilnic Inofolic, a spus ca e mai bine sa nu le combin si sa-mi vad in continuare de Inofolic.
Editat de corinka, 10 august 2016 - 18:29 .
Postat 10 august 2016 - 20:47
Eu doar mananc sanatos,numai bio(adica ce produc eu),multe proteine in special cele care contin estrogen si f multa miscare si soare(asta ca sa nu iau vit D).Dar eu nu mai sper la a obtine o sarcina cu material propriu...doar vreau sa am corpul pregatit de sarcina.
Postat 10 august 2016 - 21:09
Postat 10 august 2016 - 22:34
Postat 10 august 2016 - 22:44
Referitor la sport, am ramas cu gura cascata cand am citit asa ceva, de exemplu: http://citeseerx.ist...p=rep1&type=pdf
Din cate inteleg eu sportul dauneaza...engleza mea e mai slaba.Eu vorbeam de miscare in general,nu de facut sport intr-o sala.Miscarea pune sangele in circulatie,acesta se oxigeneaza mai ok si nu cred ca ar putea avea vreo influenta nefasta asupra nici unei boli.Daca un medic mi-ar spune ca sedentarismul ma va ajuta sa raman gravi in nici un caz nu mi-as pune c...pe o canapea si sa astept...mi se pare absurd.Nu sunt de acord cu surmenajul fizic,nici psihic.
Postat 10 august 2016 - 22:59
Postat 11 august 2016 - 10:04
Bag si eu pe fuga un cap sa va mai zic ce s-a mai studiat, ce s-a mai descoperit. Sper sa ajung la zi si cu cititul din urma.
Age-related scarring in ovaries may explain reproductive decline
Women may be losing their ability to produce healthy eggs later in life due to excessive scarring - or fibrosis - and inflammation in their ovaries, according to a study in mice published in Reproduction. These findings could pave the way for new treatments that delay ovarian ageing.
Age is the most important factor in female infertility, and older mothers (aged 35+) are more likely to suffer from miscarriages and have a higher chance of embryos with chromosomal abnormalities or children with birth defects. As women worldwide delay motherhood, research into the mechanisms underlying reproductive ageing is increasingly needed.
One of the main conditions linked to ageing organs is excessive scarring which causes the accumulation of connective tissue. This condition, commonly known as fibrosis, occurs when tissues do not regenerate or heal properly. Fibrosis interferes with normal tissue function and has been previously linked to ageing in the heart, liver and kidneys.
In this study, researchers analysed ovarian tissue from populations of reproductively "young" (equivalent to women in their early twenties) and "old" mice (equivalent to women ages 38-45). They consistently identified fibrosis in the reproductively "old" mice. This age period is associated with a decline in reproductive function and egg quality in both humans and mice, raising the question of whether fibrosis in the ovaries impacts the growth and development of healthy eggs. In some reproductively "old" mice, up to 35% of the ovarian tissue was fibrotic.
Researchers also found a type of immune cell (multinucleated macrophage giant cells) in the ovaries of reproductively "old" mice only. When found in other tissues, these cells are associated with chronic inflammation, which can also contribute to tissue damage.
"The majority of reproductive aging research is focused on the eggs themselves and trying to understand why their number and quality deteriorate," said Dr. Francesca E. Duncan, currently the Executive Director of the Center for Reproductive Science at the Northwestern University Feinberg School of Medicine. She led this study while an Assistant Professor in the Department of Anatomy and Cell Biology at the University of Kansas Medical Center. "In this study we took a different angle and instead examined the changes that occur in the environment in which the eggs develop."
"Our work establishes fibrosis and inflammation as hallmarks of the ageing ovary and lays the foundation for considering the use of anti-fibrotic or anti-inflammatory treatments to delay or counteract the impact of reproductive ageing. This has wider implications for women's health because ovarian fibrosis is a key feature of Polycystic Ovarian Syndrome (PCOS) and is also an unintended consequence of medical interventions such as chemotherapy and radiation," Duncan remarked.
The research team is currently investigating how to therapeutically target the ovarian environment to improve reproductive function.