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Chiari and pacemakers

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Hello fellow Chiarians,

I'm wondering if anyone has had experience with

pacemakers.

After having a positive tilt table test where I

fainted after about 20 mins, my cardiologist has

written to me saying that they could offer me a

pacemaker of the type DDDR (I have no idea what this

acronym means!). He said that on the tilt table, my

heart rate was fast initially but then slowed quite

considerably and my bp dropped which was when I

blacked out. He said that there were no guarantees,

but I could have a pacemaker and then they could

medicate me for tachycardia (I presume he is talking

about beta blockers).

It all seems a bit drastic to me... I thought they

would offer me medication first. If anyone has any

info or experience I'd love to hear it... especially

anybody who is living with Chiari and has a pacemaker.

I'd particularly like to know if the pacemaker helped

and how it's affected day to day life... I know it

means you can't have an MRI which is inconvenient for

us Chiarians!

Many thanks in advance,

Amy (UK)

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