numbness tingling and myeloproliferative neoplasms and myeloproliferative neoplasms | myMPNteam

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Top 10 Search Results for "numbness tingling and myeloproliferative neoplasms"

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Does Mpn Cause Peripheral Neuropathy?
A myMPNteam Member asked a question 💭

I have had peripheral neuropathy in my feet and now in my hands and forearms.

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A myMPNteam Member

It is a important to distinguish the different types of numbness-tingling that can occur in relation to MPNs and their treatment.

MPN related paresthesia is a known phenomenon. While not… read more

Does Anybody Has Ringing In Ears With ET??
A myMPNteam Member asked a question 💭
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A myMPNteam Member

I have continuous ringinging in ear and my doc says it's nothing to do with MPN. But I think it is because of low blood flow in head and neck
What could be the possible reasons of this ringing in… read more

MDS A MPN?
A myMPNteam Member asked a question 💭

My father had Mylodysplastic Syndrome (MDS). Is this considered a MPN?He died from leukemia in the end. He was diagnosed 10 months prior.

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A myMPNteam Member

I and several other people on here have MDS and MPN and JAK2 mutation as well as other mutations. Leukemia is what we’ve been trying to avoid with treatment. Some have less or more of a propensity to… read more

I Asked My Dr If My ET Could Be Myelofibrosis? Dr Said "since My WBC Is Normal And I Have No Anemia, It Is Unlikely. Do I Do The BMB Or Not?
A myMPNteam Member asked a question 💭
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A myMPNteam Member

Dear Renee,

The 2016 WHO classification and diagnostic criteria for myeloproliferative neoplasms always includes a bone marrow biopsy to distinguish between ET/PV and PMF
https://www.ncbi.nlm.nih.g… read more

Does Anyone Here Know If JAK2 Inhibitor Meds Work If You Are JAK2 Negative? Just Curious...I'll Ask My Doc Next Visit As Well.
A myMPNteam Member asked a question 💭
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A myMPNteam Member

I have MF with negative Jak2. I take Jakafi. Goal is to decrease my spleen size. I will not know if working till after six months. I'm about to enter my 5th month this month (Aug)

Has Anyone Had Ringing/humming In The Ears? It’s Continuous And Has Been Going On For A Few Weeks?
A myMPNteam Member asked a question 💭
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A myMPNteam Member

Hi Edna,

Tinnitus in ET and PV is considered to be due to too many blood cells (platelets in ET and red blood cells in PV) in the blood vessels
"ET may also cause hearing problems, such as tinnitus… read more

Can PV Ever Be Cured?
A myMPNteam Member asked a question 💭
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A myMPNteam Member

The official information is that there is no cure. I could read about the odd case that went into remission, but that seems to be more the exception than the rule. Several of those cases needed bone… read more

Anyone With Familial MPN? My 27 Y/o Was Just Diagnosed With ET Nearly One Year After Me, 52 Y/o.
A myMPNteam Member asked a question 💭
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A myMPNteam Member

Here's another source to consider. It's a 2017 scholarly article that discusses familial cases of MPNs (genetic predisposition. The authors say this: “In our experience, about 7% to 8% of patients… read more

How Many Are On Disability Because Of Their Condition?
A myMPNteam Member asked a question 💭

I was diagnosed with Polycythemia Vera in Jan 2024.

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A myMPNteam Member

I receive disability for multiple conditions

I Have Continuous Ringing In Ear And My Doc Says It's Nothing To Do With MPN. But I Think It Is Because Of Low Blood Flow In Head.
A myMPNteam Member asked a question 💭

I have continuous ringing in ear and my doc says it's nothing to do with MPN. But I think it is because of low blood flow in head and neck.
What could be the possible reasons of this ringing in the ears??

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View reactions
A myMPNteam Member

I've got big time ringing too, but some of it is from all the loud music over the years. Having ET has definitely made it worse. Over the years I have gotten used to it and I'm able to put it out of… read more