Jakafi

[Anouchka]

Hi All, lost the plot again because of hospital stay and info coming at me from all sides. Is Jakafi actually a chemo treatment for my PV diagnosis?

TIA for your insights.

Hope you’re all doing well.

[ainslie]

it’s not chemo

[Anouchka in reply to ainslie]

Thank You!!

[hunter5582]

Jakafi is not chemo. It is in the class of JAK Inhibitors.

[Anouchka in reply to hunter5582]

Thank you Hunterh5582 for getting back too me. Keep well!

[Spanelmad]

Hope you feel less overwhelmed now, and hopefully out of hospital

[Anouchka in reply to Spanelmad]

Thank you. I’m indeed out of hospital but not quite out of the woods yet. 🤞🏼🤞🏼🤞🏼

[lizzziep]

Hope you’re feeling better soon!

[Anouchka in reply to lizzziep]

Thank you. Hope all well with you.

[LFCLove]

Glad to hear you’re out of hospital. Give yourself time to go through all the “data” coming at you and try to relax. Remember it’s a marathon, not a sprint.

And we are all here to try to pick us up when we falter.

G.

[Anouchka]

😊😊 thank you for your encouraging words

[Lallybroch1]

I am om Jakavi, for Primary Myelofibrosis, i was told it is a targeted chemotherapy drug, and ive been taking it for a year now. I am classed as immuno supressed due to taking it.

[Anouchka in reply to Lallybroch1]

That’s interesting but maybe it ass also to do with your MPN …. I’ve got PV but a friend here has myelofibrosis but we’ve not got round to our respective meds …

Thank you for your input. Be well.