night sweats and mpns and myeloproliferative neoplasms | myMPNteam

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Top 10 Search Results for "night sweats and mpns"

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Does Anyone Get Phlebotomy As Their Only Treatment. Also Does Anyone Have Issues With Instant Recall For New Laws And Procedures, For Work?
A myMPNteam Member asked a question 💭

I have PV JAK 2 positive. My numbers have not gotten too high. I get pins and needles itching and and I’m tired. At work I have issues with instant recall of new laws and procedures.

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A myMPNteam Member

Thank you Tta, this list of symptoms really helps.

Do Others With Just ET Have Persistent And Nightly Night Sweats? A Nurse Had Said That Night Sweats Don't Normally Occur With ET.
A myMPNteam Member asked a question 💭
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A myMPNteam Member

You have below a list of symptoms present in MPNs, ET included. Several other studies found that risk score and symptom severity are not necessarily overlapping, meaning that it is possible for… read more

Has Anyone Experienced Bone/joint Pain? I Am Still Waiting On My Bone Marrow Biopsy Results But Was Diagnosed With ET + JAK2
A myMPNteam Member asked a question 💭
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A myMPNteam Member

I have hip pain... keeps me up at night. No clue if it's arthritis, bursitis, or just joint pain from ET. I'm going to see the osteo doc soon.

I Have Persistent Nausea And Retching That Happens Regularly. Is Anyone Else Experiencing This Too? Or Is This Related To Another Condition?
A myMPNteam Member asked a question 💭

I found out I have hypothyroidism, I had a hysterectomy in November. It is not as bad as last year, but continues to happen. Was hoping someone can provide some guideance.

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A myMPNteam Member

Regarding thyroid: I've been treated for Hashimoto's thyroiditis for 40 years. 100 mcg of Synthroid has kept my thyroid level normal, ever since the correct dosage was found. Also: Does… read more

Wondering If Abdominal Issues..stomach Aches And Often General Abdominal Discomfort Is Related To ET Or Just Another 80 Yr Old Body Issue?
A myMPNteam Member asked a question 💭
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A myMPNteam Member

Hi Pat. Causation is difficult. I have had a sensitive stomach for years, long before ET was diagnosed in 2022. I think it comes from being a high-performing but anxious person. For me, a nighttime… read more

Brain Fog
A myMPNteam Member asked a question 💭

I have been diagnosed with ET 4 months ago, my platelets are at 900.000, I have what I'm guessing is brain fog. Anyone every have it? Is it due to being under stress? This weekend, Easter, I forgot single things, a lot!!! I'm a little stressed. Is it just stress and my ET? Does this new symptom mean my platelets are increasing? Is this what brain fog is? Worrying a little bit if simple things I forget.

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A myMPNteam Member

If that is an option, take it. You can get support for cognitive dysfunction and that makes life easier.

Anyone Else Experiencing Memory Issues? Not Age Related But Connected To This Cancer?
A myMPNteam Member asked a question 💭
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A myMPNteam Member

Yes, I definitely have memory issues!! I'm afraid it's from the ET itself or the HU. I feel so self-conscious when I'm talking to someone + I forget a word or 2, or even forget what I'm talking… read more

Hi All Recently Diagnosed With ET Jak 2 Pos Lately I've Been Waking Up In The Night Sweating And My Bones Are Hurting Is It Related To ET?
A myMPNteam Member asked a question 💭
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A myMPNteam Member

Yes, i would say so. Jakafi medication stopped my inflammation so i have no more night sweats. No longer bone pain either. We're all different but good to discuss this with your haemotologist or… read more

Is There A Way, A Test, Blood Test, Etc. To Find Out When We Actually Acquired Our MPN, And/or When It Activated Itself?
A myMPNteam Member asked a question 💭

Many of us myself included have said we noticed changes in our bodies and self and symptoms long before we were actually diagnosed.

This bothers me bc I want and need to know, as do we all.

It’s wrong to go by the date we were diagnosed.

Anyone? Thoughts?🤔

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A myMPNteam Member

Depending on the type of mutation you have, you can sometimes distinguish between inherited and spontaneous, as well as using VAF % between different testings (it is good to repeat the genetic testing… read more

My Chiro Who’s Also A Functional Med Dr. And Renowned Worldwide For Both Said That SOP And Stem Cells Together Fix Blood Disorders, MPNs.
A myMPNteam Member asked a question 💭

🌟Anyone familiar with this
Says it’s a revolutionary specialized treatment for chronic infections, cancer, blood disorders, vitality, longevity, etc.

Apparently, many ppl do this worldwide for multiple reasons.
Reports say no known reported side effects and safe for all ages.

🌟I’m quoted it’s about $8,000 total, told the stem cells last for your life and they’re from umbilical cord blood with NO DNA from healthy babies and mothers
Said they’re tested to be safe and thankfully non- Covid… read more

A myMPNteam Member

Tatiana, I was only sharing my single person experience. I'll add, I was quite sick when I had Covid.

The trial for immunity measured 52 different 'proteins', antibodies related to sars covib2..And… read more