Puedo volver a tomar clomid ahora que han pasado más de cuatro meses de descanso?
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Our Medical Directors are outstanding physicians that you will find to be very personable and compassionate, who take care to ensure that you have the most cutting-edge fertility treatments at your disposal. This is your outlet to ask your questions to the doctors.
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Dear Patients,
I created this forum to welcome any questions you have on the topic of infertility, IVF, conception, testing, evaluation, or any related topics. I do my best to answer all questions in less than 24 hours. I know your question is important and, in many cases, I will answer within just a few hours. Thank you for taking the time to trust me with your concern.– Geoffrey Sher, MD
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No concebir con omifin
Name: Iman D
Puedo volver a tomar clomid ahora que han pasado más de cuatro meses de descanso?
Answer:
Please re-post in English!
Geoff Sher
Donación de óvulos
Name: Netzaly P
Cómo hago para ser donante de óvulos que requisitos debo cumplir para donar
Author
Answer:
Please re-post in English!
Geoff Sher
unexplained secondary infertilty
Name: CLARE TRICIA A
Dear Dr,
my husband and I have a 5year old daughter. we have been trying to get pregnant for the last 4 years but no success so far. we visited a fertility Dr and were subjected to hormonal profile test, HSG, semen analysis, heterescopy and everything was fine.
we did 4 rounds of stimulated ovulation and many eggs released but no pregnancy came
we did 2 rounds of ivf, no success
what should we do?
Author
Answer:
- UNEXPLAINED” INFERTILITY: A RATIONAL APPROACH TO MANAGEMENT
Infertility affects y 10%-15% of couples who are unable to conceive. In some cases, the cause of infertility cannot be determined using conventional diagnostic methods, leading to a diagnosis of “unexplained infertility.” However, it is important to note that in most cases labeled as “unexplained infertility,” a more thorough evaluation could have revealed an underlying cause. There are two main groups of individuals diagnosed with unexplained infertility: those without any biological problems hindering pregnancy, and those with unidentified reasons due to limited medical information or technology. Fortunately, advancements in testing techniques have made it easier to diagnose and treat infertility in the latter group.
To make a presumptive diagnosis of unexplained infertility, healthcare providers need affirmative answers to several questions. These include whether the woman is ovulating normally, whether the couple engages in regular intercourse during the periovulatory phase of the menstrual cycle, whether the fallopian tubes are normal and open, whether endometriosis can be ruled out, whether the male partner has normal semen parameters (especially sperm count and motility), and whether the presence of high concentrations of antisperm antibodies in the man or woman’s blood is associated with sperm incapacitation.
The diagnosis of unexplained infertility depends on the thoroughness of the healthcare provider in attempting to rule out all potential causes. The fewer tests conducted, the more likely it is that a presumptive diagnosis of “unexplained” infertility will be made. Below are a few causes of infertility that are often missed leading to the cause of infertility being mischaracterized as being “unexplained: :
- Subtle abnormalities involving the fallopian tubes without causing them to be “blocked”, often go unnoticed. Examples include subtle peritubal adhesions and/ or developmental or acquired defects involving the tubal fimbria (i.e., the finger-like “petals” at their outer ends), can prevent the collection and transportation of eggs to meet sperm. Detecting these conditions requires direct visualization of lesions through laparoscopy or laparotomy
- Chromosomal abnormalities in eggs or embryos can also contribute to infertility. Both eggs and embryos must contain the correct number of chromosomes (euploid) for successful fertilization and implantation. Until recently, there was no reliable method to determine their chromosomal status. However, the introduction of preimplantation genetic screening/testing (PGS/T), using genetic tests like next generation gene sequencing (NGS) has enabled the identification of embryo, numerical chromosomal abnormalities (aneuploidy) which when present will prejudice fertility. PGS/T has become an essential tool in diagnosing infertility.
- Luteinized Unruptured Follicle (LUF) Syndrome is another condition that can contribute to unexplained infertility. In this condition, eggs become trapped in the follicle and are not released, despite routine tests indicating normal ovulation. Hormonal dysfunction related to ovulation can also negatively impact the preparation of the uterine lining, hindering normal implantation.
- Immunologic implantation dysfunction (IID) can occur when the woman’s or man’s immune system attacks sperm cells, rendering them immobile or causing their destruction. Additionally, immunologic dysfunction involving the uterine lining can lead to early rejection of the implanting embryo, often before the woman realizes she has conceived.
- Cervical infection, specifically Ureaplasma Urealyticum infection of the cervical glands, can prevent sperm from reaching the eggs in the fallopian tubes. This type of infection is usually undetectable through routine examination or cervical culturing methods.
- Mild or moderate endometriosis is a condition associated with the production of “pelvic toxins” that reduce the fertilization potential of eggs. Approximately one-third of women with endometriosis also experience IID. Detecting mild or moderately severe endometriosis requires direct visualization of lesions through laparoscopy or laparotomy, and identifying IID requires sophisticated tests performed by specialized Reproductive Immunology Reference Laboratories. In some cases of early endometriosis the lesions are “nonpigmented” and cannot even be detected through direct vision, yet they can significantly impact fertility through establishing a “toxic” intrapelvic environment that compromises competency of the egg as it traverses the pelvic environment during passage from the ovary to the tube.
- Psychological factors can also influence fertility. Stress and negativity can interfere with hormonal balance and decrease the ability to conceive.
- Mild Male Factor infertility that are not readily detected through routine semen analysis.
- Antisperm antibodies (ASA) in the man or in the woman. This can only be diagnosed using high specialized blood and sperm test.
Management:
When it comes to managing “Unexplained Infertility,” a personalized approach is crucial for success. The first step is to identify any underlying causes whenever possible. For those experiencing ovulation dysfunction due to hormonal imbalances, ovulation induction with oral or injectable fertility drugs is often recommended. In cases where an IID is detected, selective immunotherapy will be required and in cases cervical mucus hostility is caused by a ureaplasma infection, specific and simultaneous antibiotic therapy becomes necessary.
For younger women (under 39 years) facing issues with sperm migration through the cervix, uterus, and fallopian tubes, intrauterine insemination (IUI) with or without controlled ovulation stimulation (COS) is often the recommended course of action. However, if these treatments prove ineffective, or if the woman is over 39 years old, has IID, harbors significant concentrations of antisperm antibodies, or has structural tubal abnormalities, IVF becomes the preferred option. In cases of male infertility that are intractable, moderate, or severe, where natural fertilization seems unlikely, injecting sperm directly into the egg through a procedure called intracytoplasmic sperm injection (ICSI)/IVF is necessary to achieve fertilization.
It is an undeniable truth that the majority of infertility cases can be diagnosed, which makes it disheartening when the label of “unexplained infertility” is used as an excuse for not conducting a thorough evaluation of the problem. Couples should not simply accept a diagnosis of “unexplained infertility” at face value. Instead, they should actively seek to have their treating physician identify the specific cause of their infertility, as treatment is most likely to be successful when the root cause is fully understood. By taking charge of their reproductive health and exploring all possible avenues, couples can increase their chances of achieving their dream of starting a family.
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PLEASE SHARE THIS WITH OTHERS AND HELP SPREAD THE WORD!!
Herewith are online links to 2 E-books recently co-authored with my partner at SFS-NY (Drew Tortoriello MD)……. for your reading pleasure:
- From In Vitro Fertilization to Family: A Journey with Sher Fertility Solutions (SFS) ; https://sherfertilitysolutions.com/sher-fertility-solutions-ebook.pdf
- Recurrent Pregnancy Loss and Unexplained IVF Failure: The Immunologic Link ;https://drive.google.com/file/d/1iYKz-EkAjMqwMa1ZcufIloRdxnAfDH8L/view
I invite you to visit my very recently launched “Podcast”, “HAVE A BABY” on RUMBLE; https://rumble.com/c/c-3304480
If you are interested in having an online consultation with me, please contact my assistant, Patti Converse at 702-533-2691 or email her at concierge@sherivf.com\
Donación de ovulos
Name: Brenda N
hola, buen día. Quería saber cuantos años tengo que tener para donar óvulos y cómo sería todo el proceso, tengo que pagar algo?
Author
Answer:
Please re-post in English!
Geoff Sher
FET inquiry
Name: Ziyi W
Hi,
My wife and I are doing IVF in Canada and going to transfer embryos to United States for surrogacy. Can I know the cost estimation of FET at your clinic? (including fees to receive embryos from other clinics, FDA screening kits for international parents etc)
Thanks!
Author
Answer:
Please call Jessie at SFS in New York (646-792-7476) for this information.
Geoff Sher
HLA matching
Name: Holly S
Hello,
I compared the markers of different HLA genes between myself and my husband from our raw genetic data which was produced by 23andMe and I found the following:
1. HLA-A: 3/3 markers matched = 100%
2. HLA-B: 2/4 markers matched = 50%
3. HLA-C: 2/2 markers matched = 100%
4. HLA-G: 2/5 markers matched = 40%
5. HLA-DQA1: 7/17 markers matched = 41%
6. HLA-DQB1: 3/9 markers matched = 33%
7. HLA-DRB1: 3/5 markers matched = 60%
8. HLA-DRB5: 9/9 markers matched = 100%
Some APA testing done and was negative. No elevation in thyroid antibodies. Normal karyotype between me and my husband.
What treatments or methods of conception would be helpful for us given this information?
A bit of background:
We have a son from a medicated timed intercourse cycle after trying for 3.5 yrs after 4 failed medicated IUIs and one failed IVF cycle. I had an elevated PAPP-A during pregnancy and uterine artery blood flow was normal, however, son was small for gestational age (basically didn’t grow much after 35 weeks). Been trying for baby #2 since 2020. Since then I have done 5 medicated timed-intercourse cycles, 6 medicated IUIs, 7 blastocysts transferred (not PGT-A tested), all in all only resulting in 2 chemical pregnancies (1 from an IUI, 1 from an FET). Had chronic endometritis and undiagnosed endometriosis all during those blastocyst transfers. I also transferred 6 cleavage stage embryos where I used lovenox, intralipids, prednisone, and other meds but no pregnancy. Endometriosis diagnosed via laparoscopy in the Fall 2023 at age 41.
Thanks in advance for your advice.
Author
Answer:
This is too complex for me to respond to authoritatively here. I request that you call my assistant, Patti Converse (702-533-2691) and set up an online consultation with me to discuss.
Geoff Sher