Sarah Bell’s Story About May-Thurner Syndrome and Blood Clots

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 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 the 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 with questions about this matter.

Photo is Sarah, husband Dustyn, and daughter AshleyAt age 26 in June 2006, I was diagnosed with a deep vein thrombosis (DVT) that extended from my ankle to my groin on my left side.  I was unable to walk, because of intense pain and swelling in my leg, and I thought I was going to die.  I was too scared to move, breathe, or do anything due to fear that one wrong move would send the clot to my lungs and kill me on the spot.

I spent a week in the hospital and was discharged on Coumadin® and compression hose.  I didn’t know the reason that I developed the blood clot, and my doctor’s only thought was that it was due to birth control pills, which I no longer take.  During this time I was doing research online about what could be done about my problem, but everything I suggested to my doctor was dismissed.

I experienced severe anxiety during the months after my hospitalization, because I believed this clot could kill me.  Moreover, my leg had not really improved; I still had swelling and pain.  I asked several times for leg scans to see what was going on, but again my doctor dismissed my requests.  In December 2006, it came time for me to come off my 6 months of Coumadin® therapy and I was scared at the idea of stopping it.  I remember having this conversation with my doctor and he said that 6 months on Coumadin was standard practice for a DVT.  I have since found out that this is more often true when the cause of the blood clot is identifiable.

My leg remained swollen and painful into the early part of the following year.  I finally convinced my doctor to order a Doppler ultrasound in February 2007 that showed another clot in my groin, and I was admitted to the hospital for another week.  My suggestions for treatment based on my reading were still dismissed.  I was told that I probably had a genetic clotting disorder, and that I would probably be on Coumadin® for life, and was also advised against any future pregnancy.  I was tested for blood clotting disorders such as factor V Leiden, and the tests were negative.

I finally realized I was more than overdue to change my primary care doctor.  I chose a new doctor who saw me during my hospitalization, and was very receptive to investigating what was going on with my leg.  I went to a hematologist, a geneticist, and all were stumped because I had no genetic clotting disorder.

My body started changing soon after this; I started developing “lumpy veins” on my lower abdomen.  I went back to the doctor and he sent me to an interventional radiologist, who took one look at my stomach and said there must be a clot in my pelvis or stomach.

He scheduled me for an immediate venogram, although, at this point, it was already February 2008, an entire year and a half after my initial DVT.  The venogram showed an 8 inch clot in my pelvis.  I had been walking around for almost 2 years with a massive clot in my stomach that extended all the way down to my ankle at one point.  I don’t remember much of what went on in the hospital that time, but I was diagnosed with May-Thurner Syndrome (MTS) for which I was given a clot busting drug and a stent was put in my vein to improve blood flow.  Unfortunately, in the time that I waited for someone to listen to me and help, there was permanent damage to my leg, and it will never be the same.

This was the first time I ever heard of MTS.  MTS occurs when the left iliac vein is compressed by the right iliac artery and creates a clot due to pooling of blood.  MTS is more common in young women, although it is a rare condition.  I believe MTS should at least be considered a possibility when a young women presents with a DVT in her left leg.  One of my hopes in telling my story is that it becomes more common practice to keep MTS in mind during assessment of a DVT in the left leg.

I am, however, still here and alive.  I am lucky that I had my daughter Ashley before this nightmare started, because it is too risky for me to have any more children.  She is truly a blessing as well as my husband, Dustyn.  I would not have made it through this without his love and support.  I will be on blood thinners and wear compression hose for life.  My other hope in telling my story is that people learn how important it is to stand their ground and demand to be listened to when dealing with healthcare professionals.  Patients are more aware of what is going on in their body, and are usually right when they sense something is wrong, even though healthcare professionals are trained as clinical experts.

Take Home Messages

  • See messages of author within her story, particularly the possibility of May Thurner Syndrome when there is a DVT in the left leg that does not resolve.
  • Be an advocate for yourself in seeking care and trust what your body is telling you.
  • Birth control pills increase risk for blood clots.

Posted December 2011

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Author: admin

49 Responses to "Sarah Bell’s Story About May-Thurner Syndrome and Blood Clots"

  1. Kelly
    Kelly Posted on September 24, 2013 at 12:23 am

    Thank you for your story. I just found out Friday I have MTS. I have had pain in my legs for 5 years but it has gradually gotten worse. In addition to MTS, the valves in my upper legs do not work either. This is a scary, painful condition and I appreciate hearing about other peoples stories.

    • danni
      danni Posted on February 4, 2014 at 11:35 pm

      Hi, I have been diagnosed with MTS for about a year now. I had a DVT 10 years, due to this DVT 9 years later I developed the signs of PTS and Chronic Venous Inefficiency (the valves in my upper legs do not work either.)Everyday day I wear a compression stocking to help with my swelling and this seems to help. No living with Lympehdema and wanting to have children I wonder what the years a head hold for me.

      MTS is uncommon and not many people in Australia have heard of it. Most GPs I speak to need me to explain what it is and i have been given the option to have a stent put in however I have decided against this. At the moment my vein only has blood flow restriction when I lie down, and why put a stent in when there’s no guarantee it will help with my leg symptoms, due to me having a Chronic Deep Vein Thrombosis which is now calcified to my vein.

      There also seems to be little research / foundations in Australia for this kind of thing. Sarah my heart goes out to, and keep strong!! If i o\coudl do something I’d love to raise awareness, money for this Vascular Disease to make sure people understand the risks associated with DVTS and how life changing they are.

      Any feedback would be appreciated.

    • barb
      barb Posted on October 31, 2014 at 5:08 pm

      Hi. Recently my daughter suffered pain in groin. Taken to er sent to another hospital with a vascular surgeon. Was the largest clot he ever seen in a healthy 18 year old. She underwent surgery three days in a row. Found she had MTS right away. Went in on a Sunday released on Friday. Put on coumidon on lovanox. Permanent stent put in vein. Thankful they cought it right away.

    • Tanya
      Tanya Posted on March 28, 2015 at 4:33 pm

      Thanks for sharing all of these stories. Glad to
      Know I am not the only one out there with May Thurner Syndrome. I had my first DVT ankle to groin
      when I was 27. Two weeks ago at 37 I have my 2nd. After losing 120 pounds I did not think this would ever happen to me again. Now here we go again. My lifestyle has changed drastically. Eat healthy, work out daily and like I said here we go again. This time around they discovered MTS so put a stent in my pelvis. Radiologist said he would have also stented my hip but can’t due to contestant movement of hip. I am now on blood thinners for life doctors say. Got off of them after weight loss for about two years. Dr said may not have seen MTS due to me carrying extra weight, so I guess that’s a blessing so they could find it. After placing first stent they took it out and put in a bigger one because they could see vein closing. Placed largest stent and still vein wanted to close. Radiologist hopes body will accept it and more blood flow will get threw. So he was not 100% happy with placement but hopes it will improve. Compression stocking to my knee also. Swelling is brutal, sore from angio still and swollen behind my knee where they put catheter in to put drugs in to bust up clot & inserted stent. Also have purple marks around my ankle and on foot where it seems to swell terribly. Still feeling really crumby and tire out so easy.

    • kaylee
      kaylee Posted on January 11, 2016 at 1:29 am

      I had the exact same issue but in my right leg from my ankel to my abdomen. I am now 26 and two kids later I have developed a seconded blood clot. They also did a factor 5 and cane out negitive. I go to see a specialist tuesday. They have had me on lovanox and warfarin but my level is still at 1.4 and I have been one the medication for weeks. I am very nervous but also looking for answers. I am glad all is well hoping I can get the some answers

  2. Kieran O Leary Ireland.
    Kieran O Leary Ireland. Posted on September 24, 2013 at 8:29 pm

    Hi Sarah, Reading your story, my heart go,s out to you. My story is the same as yours, When they discovered the cause, M T S . IIt was too late to do anything about it.

  3. Chelsea
    Chelsea Posted on September 30, 2013 at 5:20 am

    Hi Sara my name is Chelsea
    I’m 15 years old and I start having a pain where my grown area is, well within 3days I couldn’t walk without crying.! I thought something was really wrong my mom said its probably a cyist.but I couldn’t walk so she took me to the ER. It took them 2 hours to get me in a room and by then my leg was swollen and have what looked like red spiterweb all over my left leg. When I saw it I thought I was going to loss my leg. I am 15 and before this I was a regular 15 year old they took a immediate ultrasound and found I had a clot from my ankle all the way up to my lungs and yes it was solid.! When i heard the new I thought I was dieing I was so scared and the rushed me to Cooks Children’s Hospital and I had 4 surgerys back to back I have a stent by my overys and if I do get pregnant it will be life threating and that scarys me any day I could relapse I was normal before this now I have to where this tight hoes and take 2 shots a day exactly 24 hours apart.! I want to tell my story but I don’t know how

    Love The (NotSo) Normal Girl

  4. Sandi
    Sandi Posted on October 16, 2013 at 4:31 pm

    Dear Sarah,
    I had a massive blood clot in my upper left leg/groin area in 2006, age 62 I figured it out myself–stiffness & some pain (not much) in back of leg, not front. Brighter pink coloring, turning to red, rock hard on the back,and the leg almost doubled in size in the half hour getting to hospital. Also, my heart rate went up, over 130 and blood pressure was 25 points above normal. In e.r. they did a Doppler & said it was a clot, a “biggie,” but they didn’t do a C.A.T. scan. If they had, they would have found the clot(s) extending into the iliac then and diagnosed the May-Thurner Syndrome I’ve had all my life, It was found this year,June, when I had another similar situation. This time (June 2013) I got there BEFORE the clots showed up in the leg.(there were lots of them, almost one big one in entire iliac area ) Dopler showed no DVT (clot) but very restricted blood flow and the tech knew there were clots in iliac, which was confirmed with the C.A.T. scan. Twelve hours later I was in surgery for the clot-dissolving , angioplasty and insertion of a stent, a 4-hour procedure done by an excellent, pleasant but very professional team–they even asked what music I liked & played both Zydeco and classical. Vascular surgeon gave me OK to resume normal activities (iincludes dancing, playing volleyballl and a job as a landscaper/gardener) two days later. My leg, which had been slightly swollen since 2006, looks normal now, I’ve lost a few pounds without trying, remain at ideal weight and have more energy. I appreciate what the medical establishment did for me, but shouldn’t have had to wait (at great risk without knowing it) SEVEN years.

    • Betty
      Betty Posted on May 31, 2014 at 8:18 pm

      Hello Sandi. I have MTS also. My story is similar to many others. As a result of my own research and insisting on seeing an interventional radiologist my clot was dissolved within 8 days of onset and a stent was placed in my collapsed vein. The first hospital sent me home with a huge leg, pain killers, Coumadin and said good luck. The second took excellent care. I was also treated by an amazing team and skilled interventional radiologist. It’s been six months and I feel great. Leg is almost back to normal size. I take xeralto each day and wear a thigh high compression hose during the day. I’m trying to understand the necessity in wearing the hose. My blood tested fine – had nothing to do with the clot. My hematologist wants me on xeralto for one year. Are you on blood thinners? Do you wear compression hose?
      If so, have you been told it’s temporary treatment?

      Thanks so much


      • Lisa
        Lisa Posted on August 30, 2014 at 6:38 pm

        Hi Betty, I have MTS as well. I walked around for years with a swollen left leg. I was told to walk more, drink more water, and take ibuprofen. We both know that none of this worked. After four years, I was finally sent to an interventional radiologist. Sure enough, I was diagnosed with MTS. I underwent IVUS with a stent insertion eleven days ago. I was sent home with some pain medication and a date for a follow-up appt. By Thursday of this week my abdomen was distended and I was in a great deal of pain. I went back to the hospital and after two CT scans they found a clot in the stent. I am now giving myself two shots of Lovenox for the next three weeks and I’m wearing compression hose. I was told that I may have to take coumadin and I am not looking forward to it after I read about the food restrictions and the constant blood testing. Do you know why your physician chose xeralto over coumadin? I too wonder why I am wearing compression hose. This is my first clot, I don’t have a history of clots.
        Are you still wearing the hose?



  5. Pauline Mansfield
    Pauline Mansfield Posted on October 17, 2013 at 12:40 am

    Hi sarah I would love to be able to speak to u as my 18 year old daughter sara has just been diagnosed with MTS. your story is absolutely identicle to yours. Anyway help and advice would be brilliant xx

  6. Carey Drum
    Carey Drum Posted on October 17, 2013 at 11:01 pm

    Hi Sarah, I just wanted to offer that occasionally, as is my case the right side is effected! As rare as MTS is right sided is even rarer! I also waited 2 years while I fought to find someone who would listen to me.

    • Jinn Kyja
      Jinn Kyja Posted on December 10, 2014 at 2:12 am

      I’m a 42 year old male, and I had right-side MTS diagnosed a couple of years ago. That diagnosis took several years to get, on the National Health Service, in the United Kingdom.

  7. Beth
    Beth Posted on November 8, 2013 at 2:11 pm

    Well I had an unexplained DVT in my left leg June 2012. Was on coumadin for 6 months. After 14 months of my left leg continuing to hurt like bruises I went to specialist that said my leg was completely clear of clots but wanted to do pelvic CT to check for MTS. He said I definitely had MTS and sent me to cardiologist for stent procedure. On Wednesday we began with venogram and was told no MTS was seen so no stent and for now no answers. Not sure next step.

  8. Tracy
    Tracy Posted on November 20, 2013 at 5:09 pm

    I have a similar story as well. I am a 43 year old female that developed groin and lower back pain on my left side in Nov., 2012. Since I was moving at the time, I figured I had pulled a muscle, but 1 week later when my leg was red and slightly swollen, I ended up in the emergency room and admitted to the hospital. The doctors figured it was caused by birth control pills and released me 1 week later. Unfortunately, less than a week later, I was being admitted into a different hospital, and finally, 2-3 weeks later realized I had MTS as I have no blood condition for clotting. Now, 4 hospital stays, numerous cath lab procedures, and 7 stents later, I am still completely clotted up and experiencing pain and minor swelling. I was switched to Xarelto earlier this year, which has been nice, but still concerned about the pain and swelling even though I wear compression stockings 24/7. If only they had diagnosed me sooner!! It should be automatic that if a person presents with a left leg DVT, it is considered MTS until and unless something else is found. It is also very difficult and frustrating to find doctors who can help, and I live in a large metropolitan area. I definitely sympathize with all of you!

    • Sherry
      Sherry Posted on May 16, 2014 at 12:06 am

      Be careful with the Xeralto. I go to Cleveland Clinic and i just tried switching from another blood thinner to Xeralto and a side effect of the drug is lower extremities swelling. I switched back to Jantoven. Be careful!!!!

  9. Yvette
    Yvette Posted on December 12, 2013 at 10:25 pm

    Hi All,

    I wanted to cry when reading your posts. I was 21 years old when I developed by first DVT – seven days after having my beautiful son. The clots were so severe – my leg was completely purple and only had minimal blood flow. I went to bed the night before with a little pain in my groin, pain the doctors attributed to childbirth, and woke up to what would be the most difficult years of my life. I spent the better part of two years in and out of the hospital with new and old clots, a pulmonary embolus, last rites, and the list goes on. Death and I have met at the doorstep a few too many times. At that time, I was counseled that more children were out of the question. My life would be in jeopardy. That was 25 years ago. Today, I’m 46 years old and last year, took the big step and had my tubes tied so as not to risk pregnancy. It took that long to come to terms with the decision. I guess I just wanted the option even if it was a life or death decision. I was told that there are NEVER complications after such a simple surgery – boy were they wrong. I had another severe set of clots, all veins from my ankle to my groin. I spent the better part of 4 months in and out of the hospital nursing myself back to the new, new normal after this episode. I was put on a new medication called Xarelto, which did the job for me – the longer side effects are another story, but livable. In October 2013, I took a fall off a chair and landed myself in the ER to look for bleeding, broken ribs and ruptured spleen. I was so lucky that day, all things considered! The radiologist decided to include my pelvis in the contract CT! The fall was so hard, that my organs shifted and they could see clear as day that I had text book perfect May-Thurner Syndrome. Like one of the previous posts, the damage is so severe now that stents aren’t an option for me, they will have to harvest a good vein from my right leg and re-route. It makes me sad to think that another child could have been a possibility, the ability to wear tall boots, not have one pant leg tighter than the other, permanent swelling…need I say more? Today, three months later, I have a beautiful granddaughter, healthy 25 year old son and I’m truly comforted that I’m not alone in this journey! Good luck to you all!

  10. Caitlin
    Caitlin Posted on January 13, 2014 at 10:44 pm

    Sarah and all,
    There is a great group for people who have MTS on both Google (more private, around 200 members) and Facebook (still a private group with around 325 members, but less so than the Google group) that are great sources of information, support and resources for those of us with MTS. You can find them by searching for the “MAY-THURNER SYNDROME RESOURCE NETWORK” or contacting the moderator of both groups, Diane Peterson. Please come take a look for us at

  11. Bg
    Bg Posted on February 10, 2014 at 1:37 am

    I had a DVT in my pelvis, thigh and calf. It took me going to the ER twice after three docs said there was nothing wrong with me. I went to the ER (second time) and was given Coumadin and heparin shots. The next day I was resting on the couch and a doc from the ER called and tole me to head there immediately. I went to the ER and had a ct scan and a large clot was found in my pelvis and I had may Thurner. Within 30 min I was in surgery to have the clot busted in my pelvis and three days later I had two stents placed. I was in ICU for four days. If you think something isn’t right stick with it even if multiple doctors tell you your fine. If you don’t like what one says keep going to different people until someone listens to you it could save your life! My surgeon said if I hadn’t kept with a diagnosis the clot would have killed me. I also have Factor V clotting disorder and am on Coumadin the rest of my life. You can still get clots while on blood thinners. A couple months ago I had a pulmonary embolism.

  12. Donna Edgerley
    Donna Edgerley Posted on February 16, 2014 at 11:05 pm

    I was diagnosed with DVT in 2201. I had an IVC filter inserted and live amost normally with the exception of heavy bleeding, nose bleeds etc. Now at age 58 my leg began hurting and swelling .I am on 10mg of coumidin nightly and have weekly INR testing.I have experienced limitations in this past year since as standing and walking with pain; actually limping at work which is in school setting.NOne of my excellent doctors in Rhode Island could tell me what was wrong. I thought i just had a clot in my left calf. I was not prepared for what the doctor told me after a venogram this month. I have a signficant clot in my groin that will require stenting and phlebectomie. I read a lot of limited lifestyle and this conerns me. Does anyone have any experience with stenting and pain outcomes? Thanks and live well; it is life’s greatest revenge.

  13. Pam
    Pam Posted on May 8, 2014 at 4:30 pm

    I have this same issue; I was told yesterday that there is nothing at this point that can be done due to June 6, 2013 will be a year. The blood flow is using my uterus vein for blood flow which is causing intense pain in the abdomen area. I truly would like some solution; with the intense pain in my leg and now stomach area it is unbearable!!

    • Charlotte
      Charlotte Posted on May 10, 2014 at 9:04 pm

      Pam, Have you had stents placed? My blood was also using every route it could fine through my abdomen and uterus vein. My surgeons were amazed when they went in to place the 4 large stents. They said it was like a whirlwind in there.

  14. Kolby
    Kolby Posted on May 9, 2014 at 6:57 am

    Hi Sarah i was diagnosed with MTS almost 2 weeks ago i am 18 and my blood clot went from my groin down to my calf so they went in and removed 95 % of it last Tuesday i went to the Dr 2 days ago and my left leg has already formed another clot my first blood clot was the biggest clot the Dr has ever seen in his career so it’s very scary i will also be on blood thinners for life and wear those crazy tight socks

  15. Charlotte
    Charlotte Posted on May 10, 2014 at 9:01 pm

    Wow Sarah! Your story sounds identical to mine. Only difference was I was full term pregnant when diagnosed with DVT. Discovered MTS two years after her birth and then had 4 stents placed as I was clotted from heart to ankle.. I’m now 42 and have been fighting this for 6 years now. Severe valve damage from size of clot and length of time not treated. I wear stockings religiously or I am in so much pain from swelling. 10 mg Coumadin a day.

  16. Megan
    Megan Posted on May 21, 2014 at 12:43 am

    I am 16 and literally just got an MRI and CT scan yesterday and figured out one hour ago that I have MTS. I am seeing a professional this Friday to determine next steps, which can be anything from blood thinners the rest of my life to surgery. Needless to say, I’ve taken the liberty of doing all the research I can. So far, not liking what I am hearing. We are ninety percent sure I had a dissolved blood clot about 5 weeks ago so when I got my Doppler exam, nothing showed up. Then they went on to see if it was compartment syndrome and a lot has gone on until as I stated before, the results came back for MTS. I have been having these issues for a year and a half almost and just spoke up about 5 weeks ago and now all this has happened. Life altering.

  17. Lequita LeGette
    Lequita LeGette Posted on July 26, 2014 at 8:11 pm

    please…help…my Grandaughter after having twins developed MTS…we need help desperately for doctor or clinic. Where is the best place you found. We are from a small town near Tallahassee, Fl. Please
    Lequita LeGette

    • Krisan
      Krisan Posted on August 5, 2014 at 10:41 pm

      The doctor I saw that was the lifesaver was the Interventional Radiologist- he is the one with the clot busting drugs, the one that placed the IVC Filter, and the one that placed the stent. Have your GD’s doc refer you to one.

  18. Jackie
    Jackie Posted on August 14, 2014 at 8:28 pm

    Hello, thanks for your story.

    I had my leg amputated a few months ago, I had a cluster of blood clots as a result of reynaud syndrome, this caused an ischiemic foot. This is all I know. I went to A+E 5 times before they would listen to me, by then all they could do is mainstream me heparin, they were meant to keep the tube in me but there was a lot of disorganisation and they kept leaving it out, my foot went purple and so agonising i begged them to cut it off. Then the stump did not heal, eventually after months it went black and they cut off my leg. I know I don’t know much I have been mainly coping with it all as it made me lose my job and home so you know, keeping my head up, making sure i stay positive and not lose my confidence has filled my mind.

    I haven’t written it out, i only just googled ‘blood clots’ now to try to start to find out why. thank you for sharing your story xxxx

    • Lisa
      Lisa Posted on July 11, 2015 at 2:27 am

      Jackie, I recently had 5 clots from my pelvis to the knee and diagnosed with MTS. I told the vascular surgeon and hematologist that I have Raynaud’s syndrome. They both said that Raynaud’s has nothing to due with the clotting.

  19. Elisha
    Elisha Posted on August 19, 2014 at 4:53 am

    I just was released from the hospital after being there for a week for DVT and having MTS. I’m 22 years old and I’m completely afraid for the rest of my life especially when i had no idea I had this just thought I had a pinched nerve. My clot extended from my ankle to my upper stomach and butt. They wanted to send me home after a day in the hospital and told me I couldn’t walk because of the pain and that was it. Thank god for the hematologist I asked to see who saw it was so much worse than they were telling me. I’m on xarelto for at least a year but I’m so afraid that I have clots in other parts of my body they never checked. My life has been changed forever and i feel terrible for anyone else going through this.

  20. Teresa
    Teresa Posted on August 28, 2014 at 2:51 am

    Sarah – I’m amazed to read your story. This past June I had difficulty breathing and found myself exhausted after doing something as easy as walking a flight of stairs. At that point I knew something was seriously wrong. I went to my doctor who x-rayed my chest thinking my symptoms were my asthma. I disagreed but they put me on steroids for 2 weeks. Finally on week three I called them and told the doctors the steroids weren’t helping and pushed for a cat scan of my lungs. Doctors were amazed to find numerous blood clots in both my lungs bilateral. I was immediately put on Zeralto. Just two weeks ago I started to experience the same symptoms so I went to the doctor. Another cat scan found a new blood clot (Pulmonary embolism) in my left lung lower lobe.This ffinally got the doctors attention to have them scan my legs and right arm that I had experienced pain in the past. They found no blood clots in any of these extremities. Perplexed they had me meet with a hemotoligist two weeks ago that said he believed that this last clot discovered was most likely the last one of the other clots. I disagreed. My gut was telling me that my body was making the clots that were ending up in my lungs. As a result of the blood thinner I had to have emergency surgery last Friday due to loss of blood from my uterus. Last night once again I experienced difficulty breathing and exhaustion doing the smallest of tasks. My gut was telling me once again I had a new clot in my lung. I reached out to a past doctor that had seen me for 20 years and she met with me today. I do know that she is not going to stop till we find out what is causing me to get clots in my lungs. She is the one who told me today about MTS and told me to read about it online. We will do a scan in a few days to see if this is the problem. Tge more I read tge more I’m amazed! I did not have the clots present in my legs but I have severe back pain which may be a symptom for me that was overlooked since I had already had bad back pain due to 3 compressed disks in my back. I do know that it’s not a blood issue as I did not test positive to any of these disorders. Right now I can definitely say there is an angel watching over me since I had so many clots embedded in my lungs. I have been proactive for the sake of wanting to live. What amazes me most is up to this afternoon tgere was no sense of urgency in finding the problem yet I too have developed anxiety that one morning I may just not wake up. Thank you for sharing yiur story and I will keep you informed as to my future diagnosis..

  21. Mrs jackson
    Mrs jackson Posted on October 27, 2014 at 3:36 pm

    I’m A 50 year old woman who has had a swollen right leg for the past six years the first Gp I saw told me I had a bakers cyst which had burst and that the swelling was just something I had too live with!! Then about three months ago the swelling had gotten worse in my groin area so u asked another doctor about it he ordered a ultrasound and when this was done a month ago a DVT was found!! I was put on blood thinners and now for about two weeks I have been weak and have pains in both legs plus I thought I was just having my period but now it’s been two weeks of bleeding is this fine or what should I be asking my GP to check is ther something to law wrong?? I am worried please help!!

  22. Karee
    Karee Posted on January 20, 2015 at 9:12 pm

    This is my exact story except I’ve never heard of MTS. Every detail… DVT from groin to ankle, passed every genetic testing, 6 months therapy, 3 years later have “bumps” in my abdomen/pelvic area… All of it. But I’ve never heard of MTS. I don’t have a stent, but yesterday a vascular surgeon found a massive clot in my left abdomen with an ultra sound. They sent me home and said they would do a follow up MRI in 2-4 weeks. I’m not getting answers and not sure what I should be doing now.

    • barb
      barb Posted on March 26, 2015 at 2:28 am

      I had 3 massive clots in my legs before I found one doctor who has soon as she seen me knew I had mts. I immediately had 9 Stents placed in my iliac and Ivc veins. Be your own advicate not all doctors care. Don’t stop asking until you find a dr who will help you. My email address is for anyone who needs advice. My first clot was 2010 my stents were done in 2013. I still have pain and my legs will never ever be the same.

  23. laura
    laura Posted on January 25, 2015 at 3:40 am

    While what we have is horrible it is comforting to see that I am not alone. I too have M T S. At 26 weeks pregnant I clotted from my waist to my knee. My left leg was 4 in bigger then my right. I could hardly walk. I was in the hospital for almost 2 1/2 weeks. I finished my pregnancy on blood thinners and shortly after the birth of my son received a stent. three years later I became pregnant again with my daughter. the entire pregnancy I was on blood thinners. thankfully no complications. I am almost 8 years from when I clotted. I was wondering for those that had stents placed, did they ever fail?

  24. Jason
    Jason Posted on March 19, 2015 at 6:31 am

    Hey everyone, I’ve had recurrent clot…ankle to IVC at least twice since 2011 with daily roving abdominal pain and both groins. Had every lysis/angioplasty and stenting procedure known by all the best IR guys 5x and all failed in days to months. Have lots of insights and advice for anyone who is interested. 775-276-4545. 21 yr old college guy

  25. Earleen
    Earleen Posted on April 1, 2015 at 8:05 pm

    Thanks for sharing everyone. Common theme undetected and misdiagnosis. I complained for last 8 years of leg, pain , pelvic pain on the left side. Gyn and MD never sent me for an MRI. Finally in December they saw congestion. I followed up with a Vein Specialist. Just speaking with me and listening to my symptoms he said 90 % I have MTS. I researched and they completed the Pelvic US and leg US. Confirmed pooling and block. My stent placement procedure is coming up in 3 weeks. I still have plenty pain where the compression socks. I can’t wait to feel better! Thanks you for sharing best wishes to everyone!

  26. Denise
    Denise Posted on April 6, 2015 at 5:58 pm

    Same story here. I developed a massive DVT in the left groin down to my knee after having my daughter in 2013. Was in the hospital a month because of lysis treatments and angioplasties that subsequently failed. Stents clotted off. A year after my diagnosis, Cleveland clinic was able to correctly stent where the compression is and increase blood flow. The pain got better for a while, but lately it seems like im having more and more pain. No swelling though. Lots of charley horses, cramps, aches into my groin and hip, back, and where my sciatic nerve runs. I can’t get comfortable. Pain medication isn’t knocking it out. I know if I go to the ER, they will tell me I have overdone it like they usually do. This is miserable. I cannot imagine living the rest of my life with this pain from the aftermath.

  27. Sheri
    Sheri Posted on April 22, 2015 at 7:35 pm

    I must say, it is so nice to hear other people dealing with the same thing; not that I want people to be in pain and wish ill upon them, but just helps me feel somewhat normal. Much like all of you, I went to my local hospital with a swollen, discolored leg. Wasn’t really in pain, it was just hard to walk because my leg felt heavy and tired. They did an ultrasound, no blood work, and sent me home saying I probably have some half-ass syndrome because they couldn’t think of anything else. Well inevitably I was back at the hospital in 9 hours and by now my leg was so swollen, they rushed me by ambulance to another hospital so that they could perform a fasciotomy. For the next 4 days I had 3 surgeries, tubes everywhere in ICU. The doctors were not getting the results they wanted and due to the severity of the swelling, were unable to place the stents so…they life flighted me to another hospital where I underwent yet another surgery. The doctors were able to place 2 stents and 2 days later I was released from the hospital. Now, a year and a half later, I’m having pain and swelling in my left leg again and scan shows that the stent is almost completely occluded. Back to the operating room…they placed new stents (longer ones) and I stayed in the hospital for 2 days. Back for a check-up a month later and there’s another clot in the stent…admitted me, went back in to clean it out and 2 more days in the hospital. Back in 3 weeks for another check-up, same damn thing!!! Obviously by this time I am very emotional and discouraged as I am still having swelling in my leg and lots of pain/aching. Doctors (at Stanford Hospital in Palo Alto, CA) are saying, “I have them all scratching their heads”. Not really what you want to hear a doctor say. I am curious if any of you are still dealing with residual pain/aching and what you do for it???

    • Renee R.
      Renee R. Posted on April 24, 2015 at 6:18 am

      I was diagnosed in 2003 for Factor V Leiden, As well as a blood mutation disorder. (Don’t remember the name). I learned this is genetic, and also found out that’s how my uncle and 2nd cousin died. My first clots were all over my lungs as well as my left leg . It was making my leg as big as a purple tree trunk. The pain was unbearable. The hospital assigned a cardio dr to me. This dr had to try for 3 days to do the procedure without dislodging the massive clot and killing me instantly. Successfuly ,a pelvic filter , and 3 stents in my left leg. I was put on warfarin 7.5 and 12.5 doses alternating daily. As well as Lovenox shots. That recovery was awesome. I was able to work out and play sports etc. July 2014 my leg started turning purple , hot, painful. All stents were closed. After 4 days in ICU and 2 surgeries later,( which I woke up during the 2nd surgery to the dr punching the back of my leg , as if forcing the stent into place, I screamed and within seconds I was given med and knocked under ). Did anyone know that’s the worse time to be in a hospital is the first week of July? I guess all new drs who just graduated start that week. Beware .. .well they gave new stents and Angio procedures they diag me with MTS. That was the first time I had ever heard of it. I have been on xarelto and it has pros and cons. But gets the job done . However, I have been in chronic pain. I’m not getting any answers and good IR rare to find a good one. I really think my stent is too big?! I can only walk a block or 2 without hurting , and now it’s gone to my hip. I pray I find a good IR and get better results. As we all know this treatment is very expensive. I’m waiting for my new insurance to start and it’s back to the dr. It’s sad I have to risk my life and wait for insurance. I’m very scared that I will have to live in this pain for the rest of my life. I have begun feeling depressed and weight gain since I can’t continue active lifestyle. Cant ride my bike,workout or play sports .
      I guess we all need to keep pushing forward, trust ur gut. Find a good dr. I TRUELY think my stent is too large , hopefully this can be corrected! I wish everyone luck . Stay on meds. (No homeopathic alt. avail unfortunately ) I think EVERYONE having any surgery should be tested for factor v . No one deserves to go thru this.

    • Dj
      Dj Posted on October 14, 2015 at 8:23 pm

      Hi Sheri –
      Try checking out Laura Pak in Greenbrae, CA (2nd office Novato, CA) – she was the one that diagnosed my MTS right away – before the CT scan verified it. She cleaned it out, installed a stent and so far so good.
      Good luck….

  28. Katherine
    Katherine Posted on May 19, 2015 at 6:10 pm

    My first stent last 14 years without any issues but I have been through heck this past year because of occlusion in the stent causing ankle through the abdomen clotting. After numerous attempts to try and clear the stent we put in three new stents. They soon became occluded so we lysis them and decided to do a femoral to femoral bypass using the vein from my right leg. The new vein failed so we immediately went back into surgery and replaced that vein with a plastic tubing that is coated in heparin. There is no any blood flow through the new plastic vein and so we wait for the next blood clot. He said we can go directly to the problem and replace my entire iliac with the plastic tubing. He said this would make me a coach potato and I am very active. He teasingly said we could always take the leg off or at least I hope he was teasing. It was helpful reading all the post as the continued blocking of the stents seems to be a common issue with May Thurner syndrome patients. It is time they find better stents.

  29. Tina
    Tina Posted on November 2, 2015 at 4:09 pm

    I am 39 and just found out I have MTS but I have it in both legs not just my left which they said the chance of that was very rare and unusual it hurts to walk it hurts to sit and laying down is painful also I did research for both legs but there is nothing on it only in the left leg so I am scared and have no clue what will happen, does anyone know about it in both legs?

  30. Ann D'Hondt
    Ann D'Hondt Posted on November 5, 2015 at 1:55 am

    So sorry to read so many stories of misdiagnosis or lack of. I was not treated due to my age (72) in spite of MTS diagnosis from CT . It is not typical at my age! I strongly recommend Mayo Clinic in Jacksonville FL for competent, rational care/advice!

  31. Adriana
    Adriana Posted on January 14, 2016 at 4:54 am

    Hi everyone. I wish I knew what was causing my pain as most of you have been diagnosed with MTS. I had a stroke and hemorrhage in March 2015. I underwent 4 angiograms while in ICU for 25 days. Once I was home and could actually walk around I began having severe pain in the angiogram site (right femoral artery). The pain only increased in severity and spread down my leg and to what I believe is the sciatic nerve. My primary doctor does nothing for it. I know it has to do with the 4 angiograms done on AME site. Instead of getting better my condition isgetting worse. Any advice on what to tell doctor so that he will listen is appreciated.

  32. Mandy
    Mandy Posted on January 29, 2016 at 1:23 am

    I know how you feel. I spent the past year complaining to my doctor that there was something wrong with me and I needed testing done. I had been having hip pain lower back pain and what I thought to be uterus pain. I was sent to a orthopedic doc who spent 30 seconds in my room never even touched me and ordered me to go to physical therapy. Which after 4 months I was worse. Next stop OBGYN. Who put me on birth control to stopu monthly cycles. Still I was in pain. Doctor gave me cortisone shots in my back. Still no relief. December 29, 2015 the OBGYN said a hysterectomy would give me relief. I said absolutely not until Somone does an MRI or cat scan or something to rule other things out. On Jan 6, 2016 I woke up unable to walk and my left leg was 2ce the size as my right leg. Went to the doc who sent me to ER who confirmed massive clot from my abdomen to my ankle. Through my own research or should I say my mother in laws research I read a story about another lady with May Thurners. I could have wrote her story. I was transferred to a different hospital as soon as I arrived they blamed the birth control. I said no the problem started before the birth control. Next doctor was the surgeon I said look for may thurners he said its the birth control. Just so happens all the meds they gave me would not put me to sleep so I was awake and alert through the procedure. I was able to tell him that whatever he was pushing on in my abdomen was what has hurt for a year. He looked closer and replied “oh my god you are right you have may Thurners I’ve never had a patient come in with their own diagnosis before.” Doctors do need to listen to their patients more.

  33. Gary D.
    Gary D. Posted on March 10, 2016 at 12:26 am

    I am a 46 yo male diagnosed with DVT and PE’s in September 2014. The PE’s are gone but the DVT remains in my left leg from my ankle to my groin. I was referred to a hematologist who found no reason for this to happen to me. I was not given options through the Drs. I was seeing in town so did some researching and contacted Johns Hopkins and went there for a angioplasty that is now going to be a two part deal. They started at my ankle and only got to my mid thigh where they said it seemed worse. If I am able to make a trip back up there they will start from the top and work down I’m told. I’ve already missed a month and a half of work do to this and still absolutely miserable! My job requires a lot of walking which I actually enjoy but this problem is really putting me down! I’ve never heard of this syndrome and see that it is mostly woman that have replied but I am going to mention this to my Dr. and request more diagnostics because I definitely feel something just isn’t right! Thank you all for sharing and good luck! Any questions, comments or suggestions absolutely welcome! I need to get to bottom of this and try and move on with a half way normal life!

    DORIS CANO Posted on June 28, 2016 at 6:18 pm


  35. Jessica Schafer
    Jessica Schafer Posted on July 13, 2016 at 4:13 pm

    I submitted my story on MTS as well (look up Jessica Schafer) and it always amazes me how many people have MTS when just a short time ago it was relatively unheard of. I highly recommend joining this MTS group: It is a community of people with MTS sharing their stories, and asking questions. I found the pregnancy sub-group particularly helpful and there is sub-group just for men as well (MTS is much more rare in men). The people discuss treatments, symptoms, share doctor information, and advice based on their experiences. It has been a wonderful resource for me and so I want to share it with others.