are people with mpns eligible for moderna and johnson and johnson booster shots and myeloproliferative neoplasms | myMPNteam

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Top 10 Search Results for "are people with mpns eligible for moderna and johnson and johnson booster shots"

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Are Others With Well-managed ET Considering Getting A Covid Booster Shot This Fall?
A myMPNteam Member asked a question 💭

I had two Pfizer vaccine shots in the spring of 2021, a booster in Nov. of 2021 - and then actually had a very mild case of Covid this past summer (2022). I get a flu shot every fall and I’m in general good health so am not sure I need another Covid booster at this point. So I’m curious what others are doing.

A myMPNteam Member

Nope never had the first one as was still trying ti determine what was wrong . Then the clots started on people with shots already had clots
I'm like 7up never had it never will its gene therapy not… read more

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.

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

Third Dose Covid Vaccine
A myMPNteam Member asked a question 💭

Has anyone who is on Hydrea been advised to get a third full dose as opposed to booster of the covid vaccine? My hemotologist advised a third dose since I take Hydrea,but my pharmacist said the CDC is not considering Hydrea an immunosuppressive drug and thus a booster is all I need

A myMPNteam Member

I've just been to an MPN specialist who told me the Moderna booster is all I need. So far I've been told by a hematologist to get third full dose, CVS pharmacist said booster and MPN specialist said… read more

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

Has Anyone With ET On Hydrea And ASA Been Advised To Get 4th Dose Of Pfizer/Moderna Covid Vaccine?
A myMPNteam Member asked a question 💭
A myMPNteam Member

My Dr. had me get the 2nd booster.
It was the Pfizer all 4 were Pfizer.

Covid Booster Vs Full Shot
A myMPNteam Member asked a question 💭

I have PV and am on Hydrea. My hematologist has recommended a third full dose of Moderna since Hydreain his words is an immunosuppressant. An MPN specialist however just told me all that is needed is a booster of Moderna. Have any of you gotten this differing of opinions?

A myMPNteam Member

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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 💭
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

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

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?🤔

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 Husband Has Jak2 ET.COVID Question
A myMPNteam Member asked a question 💭

My husband has Jak2 ET. He’s currently sick w/COVID for 2nd time in a month. Took Paxlovid and symptoms got better. Now sick and positive again. Is ET considered an immunocompromised disorder? Seems regular docs don’t know a lot about ET.

A myMPNteam Member

Dear Debra,

Some doctors tend to minimise risks and use absolute terms. In absolute terms, someone with ET only and without treatment might not fit the bill of being immunocompromised if by… read more