vickster
Legendary Member
Bah, resurrecting this again 
I have been offered three choices to try to treat my recurrent tennis elbow and was wondering if those of you with experience of this pesky condition could offer any insight!
Very swift history - started in autumn of 2011 - not sure of cause, possibly due to riding a too big bike...anyhow, tried PT for 3 months, no better, saw specialist and then had a steroid jab in mid Jan 2012 - couple of days of pain due to the steroid flare, back to PT, all good...
Flared up again about 8 weeks ago - probably due to lugging a heavy briefcase around the globe on business trips...anyhow, 4 weeks of physio, physio says my elbow is his nemesis (never seen such stubborn TE, and is unusually in my left, and thus non dominant arm)
and back to specialist with you!
Saw specialist this afternoon and the 3 options are...
1) TE is self limiting, but could take 6 months, 12 months, 2 years to go, no way of knowing...and I still need to lug bags around the world for work
although I have now got a briefcase with wheels
2) Activated Platelet injection - not common here in the UK, done lots in the US - from what I can tell this is basically PRP. Spec says he has been doing for a year, seen a 90% success rate, insurance should cover it - BUT involves a big needle, it hurts a lot, cannot drive straight after (not an issue) and will need to be very careful for a month, then 3-6 months to get properly better
...it looks like I may have to go to Japan again in mid Sept and mid Oct (but will figure out the bag carrying, acquire a donkey, tie my arm behind my back so I am not tempted to use it or something
)
Best thing - my spec had TE, had this done and is now better!
3) Surgery - tried and tested, 90% success, similar post op protocol and recovery to the jab, covered by insurance, and can still be done if jab fails...BUT is surgery with anaesthetic and all the usual risks, would have a 3cm incision, probably hurts a lot after
I have decided to try option 2) first (less invasive and also as poor success if after failed surgery) and would like to hear from anyone else who has had TE and what treatment, especially such an injection or similar
Cheers in advance

I have been offered three choices to try to treat my recurrent tennis elbow and was wondering if those of you with experience of this pesky condition could offer any insight!
Very swift history - started in autumn of 2011 - not sure of cause, possibly due to riding a too big bike...anyhow, tried PT for 3 months, no better, saw specialist and then had a steroid jab in mid Jan 2012 - couple of days of pain due to the steroid flare, back to PT, all good...
Flared up again about 8 weeks ago - probably due to lugging a heavy briefcase around the globe on business trips...anyhow, 4 weeks of physio, physio says my elbow is his nemesis (never seen such stubborn TE, and is unusually in my left, and thus non dominant arm)
and back to specialist with you!
Saw specialist this afternoon and the 3 options are...
1) TE is self limiting, but could take 6 months, 12 months, 2 years to go, no way of knowing...and I still need to lug bags around the world for work
2) Activated Platelet injection - not common here in the UK, done lots in the US - from what I can tell this is basically PRP. Spec says he has been doing for a year, seen a 90% success rate, insurance should cover it - BUT involves a big needle, it hurts a lot, cannot drive straight after (not an issue) and will need to be very careful for a month, then 3-6 months to get properly better
...it looks like I may have to go to Japan again in mid Sept and mid Oct (but will figure out the bag carrying, acquire a donkey, tie my arm behind my back so I am not tempted to use it or something
Best thing - my spec had TE, had this done and is now better!
3) Surgery - tried and tested, 90% success, similar post op protocol and recovery to the jab, covered by insurance, and can still be done if jab fails...BUT is surgery with anaesthetic and all the usual risks, would have a 3cm incision, probably hurts a lot after
I have decided to try option 2) first (less invasive and also as poor success if after failed surgery) and would like to hear from anyone else who has had TE and what treatment, especially such an injection or similar
Cheers in advance
