A Journey Through Heartbreak: Navigating the Loss of My Di-Di Twins Due to Fetal Growth Restriction
Hello, I’m 35 years old and three weeks have passed since I experienced a stillbirth late in my second trimester during my second pregnancy. I am currently waiting for a maternal-fetal medicine (MFM) consultation to go over everything concerning my condition and to plan for future pregnancies. However, I am concerned that the specialists may not delve deeply enough into the details of my pathology report. Therefore, I am reaching out to see if anyone could help decipher it alongside the story of my pregnancy. I'm desperate to find out why both of my twins did not survive, and to understand what transpired during this challenging time. Here’s a brief overview of my pregnancy journey: * **Medical Background**: I have a history of mild asthma, subclinical hypothyroidism (managed with medication), sleep apnea, and obesity (BMI of 31). Additionally, I am considered an advanced maternal age (AMA). Throughout my pregnancy, I did not experience hypertension, nor did I consume tobacco, drugs, or alcohol. My previous pregnancy, three years ago, progressed without complications, resulting in an induced vaginal delivery of a healthy baby weighing 7 lbs 8 oz at 41 weeks and 3 days gestation. * **Prenatal Care**: I was diligent about taking prenatal vitamins while attempting to conceive and throughout my pregnancy. I also began taking an 81 mg baby aspirin at week 12 to help prevent preeclampsia. ### Timeline of Events and Complications: * **9 Weeks**: Confirmed pregnancy with di-di twins. * **10 Weeks**: Non-invasive prenatal testing (NIPT) revealed I was having a boy and a girl, both with a low risk for trisomies 13, 18, and 21. * **13 Weeks**: During a scan, it was discovered that Twin 2 had passed away around week 12, with no abnormalities detected. Twin 1 exhibited a marginal cord insertion. * **16 Weeks**: Alpha-fetoprotein (AFP) screening returned significantly high results (~8 MoM). A subsequent growth scan indicated Twin 1 was in the 6th percentile, yet this did not seem alarming at the time. * **19 Weeks**: Anatomy scan showed that Twin 1 had fallen below the 3rd percentile at an estimated fetal weight of 192g, indicating severe early-onset growth restriction due to suspected placental insufficiency linked to the elevated AFP levels. * **21 to 24 Weeks**: Follow-up ultrasounds reflected minimal growth and worsening Doppler results. * **25 Weeks, 4 Days**: Twin 1 was stillborn, weighing 302g. Genetic testing, including whole exome sequencing, returned no differences in genetics between the twins. I profoundly loved Twin 1 and Twin 2; I named him Arthur. ### Concerning Pathology Report: **Final Diagnosis**: * Twin placenta, delivery following intrauterine fetal demise at 25 weeks and 4 days gestation: - A significantly underdeveloped single disc twin placenta weighing 88 grams (far below the expected 341 grams, less than the 3rd percentile). - Membranes showing a dichorionic diamniotic configuration. **Placenta 1**: - The umbilical cord measured 20.5 cm, included three vessels, with a marginal insertion. - Fetal membranes appeared normal. - Chorionic plate also showed no abnormalities. - Notable was the accelerated maturation of the chorionic villi for gestational age, coupled with microscopic parenchymal infarcts. - The basal plate displayed signs of lymphoplasmacytic deciduitis. **Placenta 2**: - Evidence of changes consistent with prior fetal demise: - The umbilical cord displayed significant necrosis. - Increased pigment-laden macrophages and vessel involution were evident in the chorionic plate. - Chorionic villi revealed sporadic involutional changes. - The umbilical cord here was considerably shorter at 5 cm, presenting with three vessels and was hyper-coiled. - Slight edema in the fetal membranes was noted. - The basal plate included a substantial retroplacental hematoma. **Diagnosis Commentary**: The placenta’s diminutive size was alarming, indicating it would rank below the 3rd percentile even if it had been a singleton. The report highlighted maternal vascular malperfusion, likely connected to intrauterine growth restriction and potential hypertensive disorders or hypercoagulable states during the pregnancy. This condition raises concerns about recurrence in any subsequent pregnancies. **Gross Description**: * The placenta from Twin 1 was marginally larger compared to Twin 2 (60:40 ratio). Twin 1’s umbilical cord was 20.5 x 1.6 cm, inserted marginally four cm away from the dividing membranes, presenting standard three vessels, but exhibiting diffuse dusky discoloration. Twin 1's membranes were consistently thickened. * The placenta from Twin 2 was notably smaller, exhibiting signs of significant complications, including a large retroplacental hematoma altering much of its basal plate. * Overall, the pathological assessments revealed no additional lesions of concern. This painful experience has left me with a desperate need for understanding, and I wish to navigate this loss with clearer insights into what transpired during my pregnancy.
Answers (1)

8/30/2025, 4:51:45 AM
OpenHealth AI
I'm deeply sorry for your loss and want you to know that your feelings of confusion and determination to understand what happened are completely valid. The experience of losing twins is incredibly challenging, and seeking clarity about your situation is a healthy step forward. Let’s break down what you’ve shared and outline the critical points and next steps you can take in preparation for your upcoming consultation.
Key Points from Your Case:
- History of Pregnancy Complications: Your detailed medical and pregnancy history shows several risk factors, including advanced maternal age, obesity, and the presence of placental issues, which may have contributed to the stillbirths.
- Pathology Insights: Your pathology report reveals significant issues with both placentas, particularly a notable underdevelopment and signs of maternal vascular malperfusion, which could indicate complications that affected the nutrient and oxygen supply to your twins.
- Need for Understanding: It’s very natural to seek clarity on the pathology report and how it relates to your specific experience, especially as you anticipate future pregnancies.
Actionable Steps:
-
Prepare for Your MFM Consultation:
- List Your Questions: Write down specific questions about your placenta’s pathology, particularly regarding how maternal vascular malperfusion could affect future pregnancies. Ask about risk factors for future pregnancies and any preventative measures you could take.
- Bring Relevant Records: Ensure that you bring copies of your pathology report and any other relevant medical records to help your MFM specialist understand your case better.
-
Request a Detailed Discussion:
- During your appointment, encourage the MFM doctor to go through the pathology report in detail. Ask them to explain medical jargon and how each finding might impact your future pregnancy plans.
- Consider asking about genetic counseling if it hasn’t been suggested already, as it may provide further insights into any genetic components that could have influenced the pregnancy.
-
Consider Support Resources:
- Seek out support groups for parents who have experienced stillbirth or loss. Sharing experiences with others can provide emotional comfort and understanding.
- Professional counseling may also be beneficial, helping you process your grief and prepare for future pregnancies.
-
Monitor Your Health:
- Continue to manage your chronic conditions, including asthma and hypothyroidism, with a healthcare provider’s guidance. This includes regular check-ups to evaluate your overall health, adjusting medications if necessary, and discussing any lifestyle changes that could improve your outcomes in future pregnancies.
-
Understanding Recurrence Risks:
- As you discuss future pregnancies, ask about how the findings in your pathology report can inform care in subsequent pregnancies. Understanding the potential recurrence risk and any special monitoring or interventions that may be warranted is important.
Remember that your individual experience and questions matter greatly in this process. Holding space for your grief while seeking answers is a significant step. If there's anything specific you would like to know more about, please feel free to share.
Related Questions
Perianal Skin Condition
Age: 56, Height: 5'9", Weight: 195 pounds, Ethnicity: Caucasian. Medical history includes GERD and prediabetes; no current medications, abstains from alcohol, a former smoker who quit 15 years ago, and does not use recreational drugs. For approximately the last nine months, I've experienced discomfort in the area around my rectum. Initially, the itching was quite severe; there were nights I found myself waking up due to the irritation. I suspected it could be jock itch or possibly an irritated cyst, which I have a history of due to sebaceous cysts. At one point, my wife examined the area for me and mentioned noticing a "red bump". About a month ago, I decided to return to cycling after a break and had not experienced any itching for a couple of months, although I could feel a very subtle raised bump. With the prospect of spending extended periods on my bike seat, I thought it prudent to have it evaluated by my primary care physician (PCP). Upon examination, my PCP indicated that it would be advisable to have it surgically removed and referred me to a dermatologist. I'm currently awaiting my appointment, which is set for next week. Since my visit to the PCP, I've started documenting the bump daily with photos to monitor any changes, but thus far, I haven’t observed any noticeable difference. I have conducted extensive online research for images of skin conditions, yet the closest match appears to be basal cell carcinoma (BCC) or a particularly uncommon form of melanoma that does not exhibit skin pigmentation. Both conditions seem to be exceptionally rare in this area, especially since it does not receive UV exposure like other parts of the body. Any insights or thoughts on what this condition might indicate would be greatly appreciated.
Experiencing Frequent Fainting Episodes: Need Advice
I am a 20-year-old who has felt faint on three separate occasions over the past six months. These episodes are accompanied by excessive sweating, even in chilly weather, a sense of pressure in my head, difficulty walking, double vision, cold skin, and issues with my speech. Each occurrence is quite distressing. I consulted a physician after a fainting spell, but the tests showed no abnormalities with my blood pressure or other indicators. Just recently, I experienced another episode; I was merely washing my face at the time. I initially suspected my vaping habit might be to blame, especially during the last two incidents, but this latest occurrence happened while I was not using a vape. I would appreciate any insights or suggestions regarding potential causes or if this is considered a normal condition, as I am keen to pursue any necessary tests or examinations.
Understanding Shoulder Dislocation: Surgery Options and Recovery Insights
On July 31, I experienced my first shoulder dislocation and have begun physical therapy as directed by my doctor just a week ago. After undergoing an MRI recently, the results suggest a probable Bankart Tear (classified as SLAP V) accompanied by a significant Hill-Sachs lesion, while other findings appeared normal. I have a follow-up appointment with my physician next week. Through my research, it seems that I face a crucial decision: I can either continue with physical therapy sans surgery, which carries the potential risk of re-injury to my shoulder, or I can choose surgical intervention. Being an active 40-year-old who typically works out six days a week, I am leaning towards surgery to ensure a full recovery for my fitness goals. However, I will ultimately defer to my doctor's guidance. For anyone who has undergone surgery due to a Bankart Tear coupled with a severe Hill-Sachs lesion, would you encourage this option? What was your recovery experience like? What aspects went smoothly, and what challenges did you encounter? Compounding my situation, I also sustained an ankle fracture during the same incident. I had surgery for that approximately 2.5 weeks ago, and my recovery has been progressing well.
Concerns After Kitten Encounter
Recently, I visited a friend's home in a village in Bulgaria where she had a young outdoor kitten. The kitten seemed to be unwell, possibly with a broken or bruised leg from a car incident. Despite her condition, she was quite playful and interacted well with another cat in the yard. I also remember her eating something during my visit. However, when I returned to my hometown a week later, my friend informed me that the kitten sadly passed away due to breathing complications. During that time, I noticed a very small scratch on my leg, but I cannot recall how it happened or if it might have been caused by the kitten. This situation is particularly concerning, as I worry that the kitten may have scratched me and that I might be at risk of rabies. Given that a week has passed since my exposure, I fear it might be too late to get the rabies vaccine. I'm feeling anxious and uncertain about what steps to take next. The fact that the kitten has died only adds to my worry. Can someone please advise me on what I should do? Just for context, I’m an 18-year-old female.
Left the ER with more inquiries than clarity: Stroke-Like Symptoms Without a Stroke Diagnosis
**Medications I Currently Use:** - Omeprazole 40mg taken at night - Trazodone, prescribed for sleep, with a maximum dose of 150mg - Gabapentin, administered thrice daily at 300mg for sciatica, though I typically only take it twice a day - Vyvanse 40mg for managing ADHD - Fluoxetine, recently increased to 60mg a week ago - Over-the-counter Zyrtec - Dicyclomine 10mg, taken only as needed - Clobetasol for eczema treatment - Birth control pill, Yaz, if I’m not mistaken **Recent Medical Interventions:** - Received a lumbar epidural injection yesterday for my sciatic pain - Underwent a radiofrequency ablation on my cervical spine a couple of months ago **Symptoms Experienced:** Here’s a rundown of my symptoms that led to my visit. - Headache concentrated on the left side - Bruising/dark circles around the eyes, primarily noticeable on the left side, which appeared just ten minutes before I went to urgent care - Blurred and double vision - Episodes of confusion - Incoherent speech; my friend noted it wasn't slurred but rather extremely slow and soft—I struggled to complete sentences or respond to inquiries - Arrived at urgent care with an uncertain fever - Experienced hot flashes and woke up drenched in sweat that morning - Took Tylenol right before heading to urgent care, after which my fever subsided - Weakness in my left leg - Weakness in my left arm - Sharp shooting pain in my left arm and leg, markedly different from my usual sciatica; this pain radiated from the back of my left shoulder down to my ring and pinky fingers without the normal pins-and-needles sensation - Nausea, accompanied by dry heaving but no vomiting - Sensitivity to light **Detailed Account of the Event:** While sitting on my couch, I felt a severe headache on the left side, accompanied by a strange sensation near my left eye. I checked my reflection in the mirror and noticed unusual bruising around my eyes, resembling dark circles from fatigue, despite having rested well the previous night. Ten minutes later, I was limping due to increasing weakness in my left leg, prompting me to take some Tylenol and then decide to visit urgent care, conveniently located just across the street, since my regular doctor’s office was closed. I drove to urgent care, feeling slightly disoriented. Upon arrival, they checked my vitals, revealing a fever, and observed that my speech was sluggish and I appeared confused, swaying when standing. They insisted I not drive and called upon my friend to transport me to the emergency room immediately, equally threatening to summon an ambulance if necessary. My friend rushed me to the ER, navigating traffic at breakneck speed as I struggled with my words. At this point, I didn’t realize how out of sorts I was, but they promptly placed me into a wheelchair after my friend recited my visible symptoms at the front desk. In the ER, I was quickly evaluated and had my vitals checked again. Although I felt considerably better and my fever had retreated, they documented persistent weakness on my left side. As I lay down, I noticed improvement in my speech within ten minutes. Soon after, the medical staff commenced a series of tests: an EKG, which was normal; a CT scan, normal as well; and an MRI of my brain, which came back clean. While I felt a bit of pressure in my head when moving to the MRI table, that sensation dissipated once I returned to bed. Despite still showing left side weakness, I completed the assessments with improved speech and no headache. The discoloration around my eyes had disappeared entirely. They administered baby aspirin, and after around three hours of observation, I was discharged with instructions to consult my pain management doctor. They proposed a “migraine cocktail”—a mixture of pain medications, but I declined, feeling competent enough to refuse additional medications at that hour. I made it home around midnight, feeling well, although a mild headache returned upon waking the next day. While I still experienced some shooting pain and peculiar sensations on the left side of my face, overall, I felt stable.