Essential Thrombocythemia: Looking for information and support

Posted by shenriq @shenriq, Jun 4, 2018

I was recently diagnosed with Essential Thrombocythemia, a rare incurable blood cancer. Platelet count aside, I am asymptotic. This current condition morphed from (constitutional) thrombcytosis, something I’ve lived with for 25+ years. While the new diagnosis was the result of a bone marrow aspiration and biopsy, my age was an additional factor, which was completely disarming, having been walking around unwittingly for the past 8 years! While at the low end of risk for clots, heart-attacks and stroke, nothing has truly changed - except the “C” word. No chemo yet, but active discussion about hydroxyurea. Uncertainty about ET is anxiety provoking and swoethatl, but I’m feeling betrayed by my blood. I’m looking for all information about ET, the chemo and support.
Thanks!

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Profile picture for 0612judy @0612judy

I am 78 and have been on hydrea for 7 years. Periodically, The doc and I have adjusted the dose down and up as my red and white blood count drops or my platelets get too high but my count has always remained under 700 and now is in the mid 400's. I have not noticed any significant increase in infections, even after adding Prolia for osteoporosis, which also lowers your count. Healthy diet, walking, avoiding crowds, getting all my vaccinations and masking in places like the supermarket have gotten me through so far. I believe my condition is the result of moving and playing on piles of foundry fill from the local steel mill, which my Dad got free to raise the soil around our house. Back then (1950) no one understood how toxic this material was. I had two brothers who died from multiple sclerosis which I also blame on the toxic metals.

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I think we all have theories about what caused our ET. My onset was age 55. I grew up in a chemical town where they made Agent Orange and napalm back in the pre EPA days. Dad, who also got ET, worked in the plant. My college roommate, who lived a block away from me growing up, died of CMML. Two cousins lived in the same town as kids and later got leukemia.

The VA is looking at putting ET on the presumptive list for soldiers exposed to Agent Orange and Napalm in Vietnam. But it's very hard to pinpoint causes. We all get exposed to a lot of stuff over a lifetime, and it hits some people and not others.

The tendency now is to look for personal behaviors that caused cancer--smoking, drinking, aerosols, diet, inactivity, etc.,--and blame the patient for "poor lifestyle choices." I've learned that the only thing worse than having cancer is having a lack of empathy for people struggling with chronic illness.

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Profile picture for dwlowrance @dwlowrance

Thanks for your message. I was diagnosed with ET about 7 years ago at age 70 and prescribed Hydroxyurea which I take daily. My platelet count went from 1600 to 600 which satisfied my doctor and reduced the risk of clots. No other obvious outcomes so far. I hope this helps you deal with this disease for which no cause is known. I have reason to believe that my exposure to chemical weed killers may be a possible cause of the disease.

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I am 78 and have been on hydrea for 7 years. Periodically, The doc and I have adjusted the dose down and up as my red and white blood count drops or my platelets get too high but my count has always remained under 700 and now is in the mid 400's. I have not noticed any significant increase in infections, even after adding Prolia for osteoporosis, which also lowers your count. Healthy diet, walking, avoiding crowds, getting all my vaccinations and masking in places like the supermarket have gotten me through so far. I believe my condition is the result of moving and playing on piles of foundry fill from the local steel mill, which my Dad got free to raise the soil around our house. Back then (1950) no one understood how toxic this material was. I had two brothers who died from multiple sclerosis which I also blame on the toxic metals.

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now into my 4th year of HU for ET Jak2. My platelets rose for 3 years before I went to hematologist/oncologist. With HU it took a year of trial/error to get my dosage right and side effects subside plus baby aspirin. While I'm not happy about daily chemo, its better than getting stroke or heart attack. My best advice is get a good MPN Dr take care, stay safe

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Thanks for your message. I was diagnosed with ET about 7 years ago at age 70 and prescribed Hydroxyurea which I take daily. My platelet count went from 1600 to 600 which satisfied my doctor and reduced the risk of clots. No other obvious outcomes so far. I hope this helps you deal with this disease for which no cause is known. I have reason to believe that my exposure to chemical weed killers may be a possible cause of the disease.

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Profile picture for Lori, Volunteer Mentor @loribmt

Welcome to Connect, @jlore. Hydrea is a good first line medication for blood conditions such as ET. It’s been used for decades to help control over production of platelets such as you’re experiencing. I hope this works well to reduce your numbers. You mentioned there is another medication that you’d prefer but it isn’t recognized. Could you share what it is please?

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Según mi hematología es buena pero baja glóbulos rojos y blancos y por eso trae otras enfermedades.Apenas sepa bien el nombre lo paso por aquí.Gracias por su respuesta

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Profile picture for shenriq @shenriq

The side effects from the AI drugs - of which I've taken all 3 - were difficult and I opted-out! It was an emotional struggle to make that decision, but my quality of life was awful. While Tamoxifen wasn't an option, I did my due diligence and have moved on to another unrelated cancer issue.

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Cuales fueron tus nuevas opciones y quería saber si bajaron tus plaquetas

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Profile picture for jlore @jlore

Es muy útil tu comentario .A mí me diagnosticaron con trombositemia esencial desde 2020 ,hoy tengo un millón de plaquetas y el hematólogo me va a medicar con Hydrea,hoy hay una medicación mejor que esa pero la obra social no me la reconoce.

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Welcome to Connect, @jlore. Hydrea is a good first line medication for blood conditions such as ET. It’s been used for decades to help control over production of platelets such as you’re experiencing. I hope this works well to reduce your numbers. You mentioned there is another medication that you’d prefer but it isn’t recognized. Could you share what it is please?

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Profile picture for misty45 @misty45

For me, ET has meant being on Hydrea for the past 20+ years, getting a cbc every 3 months or so, and checking to make sure I have no spleen enlargement. It is a strange blood disorder because I have no symptoms that I'm aware of, however if I cut back on the Hydrea, then my platelet count zooms back up. So I have had to continue taking it and probably always will. Docs all say I will have a stroke if I don't take it and that if I don't take it, it is at my own peril.

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Es muy útil tu comentario .A mí me diagnosticaron con trombositemia esencial desde 2020 ,hoy tengo un millón de plaquetas y el hematólogo me va a medicar con Hydrea,hoy hay una medicación mejor que esa pero la obra social no me la reconoce.

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Profile picture for nyjean @nyjean

I was diagnosed with ET in November after my platelet count had been rising slowly for several years. A test showed I have the JAK2 mutation. My platelet count was 580 according to the lab, but a test in the blood doctor's office showed 450. I started taking HU daily & the last reading was 340; my doctor told me if it continued to drop the medication could be reduced to fewer days per week. Fortunately, no side effects that I've noticed.

I will see the doctor next in a few days. A few questions I want to ask him, including (1) am I now "immuno-compromised" because of the HU? and (2) if my white cells are also dropping, increasing the risk of infection, can anything be done about that?

The diagnosis was scary, but I'd been worried the rising platelets might indicate ovarian cancer (which my mother had), though I've always tested very diligently for that & everything looks good. My new gynecologist has recommended having my ovaries removed as a preventative, but I've been reluctant to do that though I'm past menopause -- but that's another issue.

For now, again, I'm very thankful to learn of this forum & will read all of the posts. It's a great resource for support, information & connection. Thank you to Lori & all who have posted & shared

Jean

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Another Jean here! 70, ET-CALR for 15 years. Have been on HU for six years. Talk to your doc about immunity suppression. I was told that, yes, it adds to compromised immunity along with age and co-morbidities. I was advised to take a daily multi vit.

I caught a bug mid-December (not covid or flu) with a cough that dragged on for 8 weeks. Husband brought it home after he did a musical presentation for preschoolers, and his was much milder and lasted a couple weeks.

But until this year's bout I haven't been sick since before covid. I keep a mask in my purse that I put on if a store seems crowded. I avoid theaters, church, and peak restaurant times. Have been vaxxed to the max. I wash hands a lot.

But that's just me. HU and compromised immunity seems to be different for everyone.

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Profile picture for nyjean @nyjean

I was diagnosed with ET in November after my platelet count had been rising slowly for several years. A test showed I have the JAK2 mutation. My platelet count was 580 according to the lab, but a test in the blood doctor's office showed 450. I started taking HU daily & the last reading was 340; my doctor told me if it continued to drop the medication could be reduced to fewer days per week. Fortunately, no side effects that I've noticed.

I will see the doctor next in a few days. A few questions I want to ask him, including (1) am I now "immuno-compromised" because of the HU? and (2) if my white cells are also dropping, increasing the risk of infection, can anything be done about that?

The diagnosis was scary, but I'd been worried the rising platelets might indicate ovarian cancer (which my mother had), though I've always tested very diligently for that & everything looks good. My new gynecologist has recommended having my ovaries removed as a preventative, but I've been reluctant to do that though I'm past menopause -- but that's another issue.

For now, again, I'm very thankful to learn of this forum & will read all of the posts. It's a great resource for support, information & connection. Thank you to Lori & all who have posted & shared

Jean

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Welcome to Connect, Jean! As you’ve discovered, there are a number of members in the forum who have Essential thrombocythemia along with the JAK2 mutation. It helps to know you’re not alone when you’ve been given a diagnosis that you may not have heard about before.
It’s really encouraging that Hydroxyurea is helping to get your platelet levels back down into the normal range so quickly. I’m sure that’s a huge relief for you! I know no one wants to be on these meds but they’re around for a reason. They work.

You may have already read some of the other posts with information about the JAK2 mutation and the conditions this acquired mutation can cause. If not, here are a couple of links for you that might be helpful.
https://www.verywellhealth.com/jak2-mutation-5217909
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https://www.healthline.com/health/primary-thrombocythemia
You have some great questions for your doctor about being immuno-compromised while using HU. Unfortunately that is one of the potential side effects of taking a medication such as HU. The medication suppresses the immune system. There’s not much you can do to change this. However, making sure you get plenty of sleep, eat healthy foods, exercise, etc…all the basics will help keep your body healthy. You’ll also want to be cautious in public or even family settings where there are a number of people gathered. It’s important to avoid exposure to illnesses, whether airborne or food related. Having Covid around helped prepare those of us who are compromised. Same protocols apply. So you may want to grab a mask to wear when you’re in an elevator, crowed store, church, etc., just to give yourself some added protection.

I’m sorry to hear about your mom and her ovarian cancer. I can understand your concern. That’s a big decision whether to have your ovaries removed or not. Have you had genetic testing to see if you carry the BRCA mutation?

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