The personal story below is intended for informational purposes only. The National Blood Clot Alliance (NBCA) holds the rights to all content that appears on its website. The use by another organization or online group of any content on NBCA’s website, including patient stories that appear here, does not imply that NBCA is connected to these other organizations or groups or condones or endorses their work. Please contact info@stoptheclot.org with questions about this matter.


My Name is HelenHelen Smith picture Smith. I’m 36 years old and have a genetic blood clotting disorder (thrombophilia) that could have taken my life twice. This is my story.

In January 2008, I delivered my third son via cesarean section. Since this would my last planned pregnancy, I also elected to have a tubal ligation performed immediately after giving birth. Both the delivery and tubal ligation went very well and without incident. It was about 2 weeks after my delivery; I experienced a sharp pain in my upper wing area of my back after I would put the baby down. I assumed it was related to sleeping on the couch, which I had done during my recovery process, as it was easier than climbing the stairs to my 2nd floor bedroom.

The pain was mostly constant, but tolerable, so while at my newborn’s check-up, I decided to ask the doctor about the pain. I mentioned sleeping on the couch, but I also thought I could be getting sick so he checked my lungs. Everything appeared to be ok.

A few days later, while out shopping, the pain became progressively worse, very sharp, and at times it was difficult to breathe. Later that night, my mother argued with me to convince me go to the hospital to get it checked out. Of course, I argued that it was Valentine’s Day and brushed it off as something that couldn’t be serious. Ultimately, I gave in and went to the emergency room.

I provided the emergency room (ER) doctor with all of the details leading to my ER visit. He then ordered a CT-Scan with Contrast (an x-ray that takes detailed picture of the lungs). The CT-Scan revealed multiple small emboli (blood clots – plural of embolism) in both lungs. I was immediately admitted to the hospital, and anticoagulant (blood thinners) medication was provided in the hospital for a few days. I took anticoagulant medication for approximately 7 months after leaving the hospital.

After what I believed to be an isolated incident of PE due to surgery, it happened again!

In April 2010, the terrifying ordeal came knocking on my door again. It was an ordinary day in April, and I went to see my middle son’s soccer game. During the game, I felt a sharp pain in my chest especially when I took a deep breath in, or if I hiccupped. Again, I thought maybe I slept wrong. I went home after the game and took a muscle relaxer and lay down. After I woke up, the pain remained, so I immediately called my doctor.

After explaining the symptoms and in light of my history of PE, he recommended that I go to the emergency room.

The emergency room doctor checked my heart and performed some blood work. My D-dimer came back slightly abnormal. As a precaution, he ordered a CT-Scan to rule out Pulmonary Embolism (PE). To the doctor’s surprise, the results came back positive for PEs in my right lung — both the upper and lower lobes. He was truly shocked, since my vital signs (blood pressure and pulse) appeared to be within normal range. Once again, I was admitted to the hospital and started on anticoagulants. This time, however, I will be on them indefinitely.

After following up with a hematologist, I learned that my family has Prothrombin Gene Mutation (Factor II) (a genetic clotting condition). The doctor believes it was inherited through my mother, who also has a history of DVT and PE, but it didn’t reveal itself until she was at an older age. As a result of my experience with this, we now know that my brother, 3 sisters, and my nephews also have the condition.

We are in the process of getting my children and other family members tested. I am so thankful to know about this condition and getting a second chance at life. My recommendation is you know your body and if something doesn’t feel right go get it checked out! Waiting could cost you your life! It is my mission to share my story and learn as much as I can about clotting disorders to help STOP BLOOD CLOTS!

Take Home Messages:

  • Surgery is a risk factor for blood clots
  • Recently giving birth is a risk factor for blood clots
  • 30% of people who have a PE will have another one
  • If you have symptoms of a PE, it is important to tell the doctor about your past history of blood clots
  • If you have pain in your upper back and chest, pain when you try to breathe, and increase pain when you lay down, these are symptoms of a PE and you should consider going to an emergency room
  • Prothrombin Gene Mutation (Factor II) is a hereditary clotting condition that gives people a greater chance of experiencing blood clots, and often affects other family members
  • If you have a clotting disorder, you need to know the symptoms of DVTs and PEs so you can see a doctor or get help as soon as possible
  • If you have a genetic clotting disorder, you may have to be on anticoagulants to prevent more blood clots
  • As Helen said “you know your body and if something doesn’t feel right go get it checked out! Waiting could cost you your life!”
  • Sharing stories about blood clots increases awareness and can help stop unnecessary blood clots
Author: admin

2 Responses to "Helen Smith’s Blood Clot Story"

  1. Juan
    Juan Posted on March 17, 2014 at 7:28 pm

    Hi Helen,

    I read your story. Glad to know you’re okay. I am new to the blog and a recent survivor of blood clots and bilateral PE. I wrote my story and I’m just waiting for it to be posted. I pray for your continued good health.

    Juan

  2. Anthony
    Anthony Posted on September 14, 2014 at 7:31 am

    I too have been treated twice for clots and will be on Coumadin the rest of my life. They checked for genetic disorder but later threw out the results because the tests were done while taking Coumadin . I have many questions and often feel alone with my problem. If anyone with similar experience would like a pen pal to talk about it feel free to email.