Celtic background & thalassaemia: Hi, When we... - MPN Voice

MPN Voice

10,887 members15,205 posts

Celtic background & thalassaemia

Vicky_b profile image
28 Replies

Hi,

When we were at guys prof Harrison mentioned a link between having a celtic background & mild thalassaemia. Does anyone have this?

We had genetic tests done & I suppose this will show it up

Written by
Vicky_b profile image
Vicky_b
To view profiles and participate in discussions please or .
28 Replies
mhos61 profile image
mhos61

Not heard that before!

I know there’s a link between haemochromatosis and Celtic background. I find that very interesting, as I have Irish heritage.

Swede profile image
Swede

Hi,no I am Scandinavian without any Celtic blood for atleast 5 generations back.

jointpain profile image
jointpain

My wife has been diagnosed with myelofibrosis. Though she has just had a BMB last Tuesday, so results not for two weeks+. She was tested in France and is JAK2+ she only really has high platelets, and of course now no spleen. Being a Welsh girl, she is probably Celtic in origin.

Lab-Rat profile image
Lab-Rat in reply tojointpain

I am sorry your wife has MF. I have read your posts and you have been through so much. I am interested to know how the diagnosis of MF was made when results of BMB are still pending? All the best to you.

jointpain profile image
jointpain in reply toLab-Rat

The diagnosis was made by a French hematologist, after a bone marrow biopsy from the sternum, though it was apparently contaminated by blood. The hematologist here said that sternum biopsies had been phased out forty years ago in Wales. We asked, and he wanted to, verify the diagnosis, which is why my wife had it done last Tuesday, with no bruising and absolutely no pain at all, during and after. Hope that satisfies your curiosity! It will hopefully satisfy ours, as she never really had any symptoms before the 1st May, other than her bp had risen over six months and she was getting a red face when she got hot. Best wishes xx

Lab-Rat profile image
Lab-Rat in reply tojointpain

Sternum biopsy, how traumatic. Please let us know the outcome of the recent BMB. Btw I am 3d generation living in South Africa of Scottish/German/French ancestry...

Lab-Rat profile image
Lab-Rat in reply toLab-Rat

ET Jak2+

Mallard profile image
Mallard

I have ET jak+ and I am Northern Irish 🍀

bordeauxgirl profile image
bordeauxgirl

This is very interesting , my husbands visiting cardiac nurse told us if you have Irish ancestry you are very susceptible to PV especially, I have PV +jak2. My DNA says I am 48 % Irish, The nurse said her husband and his father, both Irish, have the condition. I wonder why?

Vicky_b profile image
Vicky_b in reply tobordeauxgirl

I can only think it must be in the genes

westlieght profile image
westlieght in reply toVicky_b

Well am Devonshire born in Devon ! not sure of Irish ancestry !have post ET/MF sure of being 95%Devonshire small Welsh 5%?

CommonDaisy profile image
CommonDaisy

Hm this is interesting! I have ET and I’m Australian but have Irish heritage.

fernie profile image
fernie

I'm Scottish/Irish decent and also carry a haemochromatosis gene.

Wyebird profile image
Wyebird

Hi I’m at least 50% welsh

katiewalsh profile image
katiewalsh

Hi. My father was Irish, and maybe something else but not my mother. I’m ET JAK2+ Katie

At the London Patients Forum last year Dr MF McMullin an epidemiologist from Belfast mentioned Celtic heritage, but as far as I can remember it was related to haemochromatosis as another poster has mentioned. Very interested to find out more, I am half Irish.

SDJD profile image
SDJD

I have ET Jak 2+ and my father was from N Ireland. Interesting!

Suzy

Vicky_b profile image
Vicky_b

I'm going to check with guys incase i remembered it wrong. There was lots to take in!

Mica11 profile image
Mica11

I'm Scottish/Irish/German/English decent....as far back as I have checked. Interesting!

spaniels2conies profile image
spaniels2conies

Yes,interesting! I have ET Jak 2+ and my father was Scottish.

kp27kathleen profile image
kp27kathleen

Wow! My ancestry says 100% Irish Ulster and I have ET Jak2+. I live in US. I am having health DNA done and will report back

fee13 profile image
fee13

I'm Irish/Scottish decent, ET JAK2+ and haemochromatosis is in the family, I'm a single carrier so can only pass the gene down.

Vicky_b profile image
Vicky_b

I checked with guys and its thalassaemia thats linked to celtic blood not thrombocythaemia. Sorry for the confusion!

mhos61 profile image
mhos61

Thanks for the clarification on this matter.

Sheryljean profile image
Sheryljean

Vicky,

This is so interesting for this is the first time I have seen thalassmasia in any discussions. This is what I was first diagnosed with and then came PV. My hematologist was asking if I Mediterranean background and not Celtic. Since I did the dna tear I do have more Celtic background and also German. Will have to be sure to follow for fighter info so that I can pass along to my doctors. Good luck.,

Sheryl

Vicky_b profile image
Vicky_b in reply toSheryljean

Hi. Thats interesting. Are you jak2 positive?

Sheryljean profile image
Sheryljean in reply toVicky_b

Yes..this too

Sheryljean profile image
Sheryljean

Vicky,

Where and who is Dr. Harrison??

Thank you,

Sheryl

Not what you're looking for?

You may also like...

Using T-Cells To Fight MPN - CALR And JAK2 Vaccine

Being developed by the Danish team at Copenhagen University hospital. Professor Mads Hald Anderson...
PVReporter profile image

Has anyone had a bone marrow transplant who has PV?

My husband has PV he was diagnosed in 2012. He's had a scan and his spleen has doubled in size....
tracey13 profile image

Kindness matters

I am fairly new here (one year post-diagnosis) but have a comment to share after reading recent...
doglover57 profile image

Something to make you smile

I hope this Pam Ayres (or maybe not by Pam Ayres - see below) poem will make you smile. It was...
Ebot profile image

Let's start loving one another again

I know we are all worried at the moment about how the virus may affect us and our loved ones. This...
jillydabrat profile image

Moderation team

Debinha profile image
DebinhaAdministrator
Mazcd profile image
MazcdPartner

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.