I was diagnosed with hyperemesis gravidarum (HG) during my second pregnancy, which resulted in many complications, including kidney injury and an IUGR baby, and ultimately, led to an emergency C-section due to oligohydramnios. It was an incredibly difficult time, especially since no one in my region of Oman understood what was happening to me or listened, particularly after the birth. I was even sent to a psychiatric ward, where I found no relief.

After giving birth, I began experiencing serious symptoms: insomnia, anger issues, balance problems, sudden falls, and, later, memory loss.
When I discovered the HER Foundation on Instagram, I began attending the monthly HG trauma Support Group. I found others who understand.
And, I learned about the importance of taking thiamin (vitamin B1). Then I realized I was showing signs of Wernicke’s encephalopathy and started taking benfotiamine (a form of thiamin). An MRI later showed an enlarged pineal gland affecting melatonin production. After increasing my thiamin dose to 1000 mg daily, a repeat MRI showed normal findings.
The HER Foundation played a vital role in my recovery. ~Tala
Tala’s HG recovery

Today, I am better. My memory has returned, my thinking is clear, I feel rational and calm, and I am no longer angry. Now, I can go out, drive again without feeling like I’m floating, and can learn and memorize normally.
I am deeply grateful to the HER Foundation and especially to Kimber, who was a huge part of my recovery. I truly could not have done this without HER. HG introduced me to wonderful people who are miles away, yet stood by me every step of the way.
GET INVOLVED
- Share your story.
- Become a HER Foundation volunteer.
- Participate in HG research.
- Become an advocate.
- Make a gift to the HER Foundation.
- Support other HG survivors.
- Share HER resources with local health professionals and hospitals.


