Essential Thrombocythemia (ET) and viruses
I was diagnosed with Essential Thrombocythemia a few months ago, and I’m positive for JAK 2. So far, I have a “mild” case (platelets are below 600) and currently taking only 2 low-dose aspirin a day. Since my diagnosis I’ve gotten 2 colds/viruses. The first one turned into pneumonia, and I’ve never had pneumonia in my life; I’m currently sick with another cold or virus and on day 6. I feel like it’s getting progressively worse each day instead of better. Is this because of the ET? Is this how every little illness is going to be from now on?
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My MPV was high so I had very large platelets. I started to take black seed oil and my numbers actually decreased.
I was diagnosed with Essential Thrombocythemia Hemorrhage in 01/2009 during my yearly physical. My doctor prescribed me 500mg of Hydroxy a day and referred to a oncologist. I was examined intensely for about three months. I was 55 then. The oncologist talked to me about my life over many years and took blood panels twice a week. He brought me to tears. This disease would make me ill for short periods and then disappear. I had issues since a teanager, particularly acid indigestion, unexplainable psychological incidents and other odd things periodically. Not often, and I didn't know how to explain it to anyone. The Doctor asked, before telling me the issue ," You thought you were losing your mind ". I said yea, kind of. He said you were not, it was this disease, i cried,. "Everything you spoke about and more it causes". He said some doctors claim they can treat it but can't. It can cause so many different issues they will diagnose them as something else going on when it's not and cause a disastrous situation. . He increased my dosage from I pill a day to alternate with 2 every other day. The pills made me terribly ill and the worse pain in my life. I was having acid attacks. It took time and lots of suffering before it stopped. Now 14 years later I take two a day. My platelet count stay around 300. I have no issues at all. I don't believe the pills do the trick alone. I taught myself to eat a anti inflammatory diet and other foods that work with my condition. I fast two weeks, every four months.( My choice was the Master Cleanse). I am 70 years old , I look as young as 40 , not a day over 50. I got covid at least twice and never had any symptom. My hematologist see me twice a week for immunotherapy support by infusion. I credit the most, WHAT I EAT AND REFUSE TO EAT. I DON'T CHEAT. IT'S NOT OVER NIGHT, IT'S A PROCESS. THERE'S SO MUCH GOOD STUFF THAT'S AS GOOD AS MEDICINE. IT'S NOT A OVERNIGHT THING. TAKE YOUR TIME AND HAVE FUN. IF YOU DO IT RIGHT , YOUR AGEING WILL SLOW DOWN AND YOU'LL STAMINA WILL INCREASE. ONE MORE THING, IF YOU INVEST IN A GOOD ELLIPTICAL. START OUT DOING ONE MINUTE TWICE A DAY, NOT A SECOND MORE. INCREASE IT BY ONE MINUTE ONCE A MONTH, NOT A SECOND MORE, STAY CONSISTENT, WHEN YOU GET TO TEN MINUTES, STAY THERE. YOUR MIND BODY AND SOUL WILL BE FULLY REJUVENATED. YOU WILL ALWAYS BE THE CENTER OF THE CONVERSATION, FRIENDS AND FAMILY WILL NOTICE BEFORE YOU. YOU WILL BE ADDICTED TO THE REGIMENT AND FEELING SO GOOD, HELL YEA. IT'S EASY.
I agree. It took my body a year to stop the side effects. Some were worse than others....I'm in year 4 now.
I had a TIA at the end of 2014. After seeing many Doctors one Doctor referred me to a hematologist. Who is also called an oncologist. I have chrons and most of the past 9 years I have been anemic and I would just go and have an iron infusion. I usually have low red blood, white, hematocrit but high platelets. I have infusions for chrons also. I was looking for something on my My Chart and found I had Essential (hemorrhagic) thrombocythemia. I have so many conditions on My Chart I never noticed it. I never really fill great but I thought it was because of my chron and fibromyalgia. My Oncologist has never suggested I take anything for this disease and never really mentioned it. I can't take asprin because of chrons. I do take a blood thinner which was prescribed by another Doctor. I am usually given a choice of whether to come back to the Doctor in a month and a half or three months. I just thought if I get to feeling too bad I would just make an appointment and have another iron infusion. Does the name ( hemorrhagic) make the disease I have different from essential thrombocythemia?
I am curious as to what foods you eat and what foods you refuse to eat? I am struggling with sweets. Other than that I remain on a very healthy diet.
I have a question, my sons cbc is constantly abnormal. All fighter cells high and high platelets. Dr confirmed he had mild case of what ur talking about. He’s been sick for 7 months and no specialist knows why. He has chiari 1 if that helps. Can it be an autoimmune issue?
I just posted below and m son (27) has that also on cbc
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I am also curious to what foods you eat & don’t eat. This is my second request.
I just avoid sugar and anything artificial. I don’t eat anything enriched or fortified because they are synthetic vitamins. I also have the MTHFR gene mutation so I cannot process folic acid (synthetic vitamins made in a lab) I use the Walmart organic flour or King Arthur (the red one) they are not enriched. I also have to look for organic or imported noodles that are not enriched with folic acid. ALDIs has organic noodles that I can eat.