Theragun Massager TSV 04/10/21

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It will be interesting to see the price as they’re also sold on Amazon … not that I want one.
 

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They had this in my shopping centre demoing on passers by. It was very firm like a bullet pummelling if you had fibromyalgia I can see this being very painful...
 
Theragun Mini Massager with Supersoft Attachment
Item Number: 721698
QVC Price £200.00
Todays Special Value Price £164.88
P&P £3.95

Theragun Mini is a pocket-sized, agile massage device designed to provide quality deep muscle treatment to help temporarily relax tension, relieve muscle soreness experienced post-exercise and increase flexibility, plus it comes complete with the Supersoft attachment created specifically for areas of the body that need a lighter touch. Compact yet powerful, soothe and massage muscles wherever you are with the Theragun Mini.


  • Delivered to UK Mainland only

Goes wherever you do - the small size of this device makes it easy to take on trips away, keep in your gym bag or even take out walking or running with you. The long battery life offers 150 minutes of continuous use, so it will always be there when you need it.


For your workouts - the Theragun Mini is ideal to use pre and post-workout to temporarily relive tension, soreness and stiffness in your muscles. With shown results, in a study of 40 athletes aged between 24 - 27 showed Theragun percussive therapy accelerated recovery from exercise when compared to foam rolling or vibration.


Small yet powerful - a QX35 motor with QuietForce technology helps to harness the powerful, practically silent treatment, while three speeds help you choose the correct pressure for your muscle groups.


  • Ergonomic grip
  • 3 speeds: 1750/2100/2400 percussions per minute
  • 150 minutes of continuous use

Choose your colour:

  • Black
  • Desert Rose
  • White

What's in the box?

  • 1 x Theragun Mini
  • 1 x Standard Ball attachment - perfect for overall use on large and small muscle groups
  • 1 x SuperSoft attachment - for sensitive areas
  • 1 x soft case
  • 1 x power adapter

How to use:

  • To turn on the Theragun Mini, firmly press and hold the multi-functional power/speed button on the right side of the device for two seconds
  • Float the device across areas in need of treatment making perpendicular contact with the skin, gradually applying light to moderate pressure as needed
  • Only the attachment of the device should make contact with the skin. Do not use the device at an angle that puts the percussive arm of the device in contact with the skin
  • To toggle between the speeds, press the power/speed button again
  • To turn off, firmly press and hold the power/speed button until the device shuts off
  • To connect an attachment, align the attachment with the tip of the rotating arm and push to connect
  • To remove an attachment, grip the attachment, placing one finger on each side of the plastic connector, and pull off the attachment

 
They had this in my shopping centre demoing on passers by. It was very firm like a bullet pummelling if you had fibromyalgia I can see this being very painful...

Excuse me being personal but do you have Fibromyalgia? Feel free to reply by PM. Not asking for a friend. 😢
 
Hmmmm, TSV PRICE £164.88 QVC price after today £200, yet Jill Franks said that on the High Street it would be £175. ergo not much saving with p & p on High Street price, so why is QVC charging £25 MORE than the High Street after today ???
 
Hmmmm, TSV PRICE £164.88 QVC price after today £200, yet Jill Franks said that on the High Street it would be £175. ergo not much saving with p & p on High Street price, so why is QVC charging £25 MORE than the High Street after today ???

There are extra heads with the Q.

I've wondered do the extra heads fit in the case? Would be daft to have a case with attachments outside that are bound to part ways.
 
I tell you what it feels like someone shooting a rubber bullet into your body. its very painful.
 
Yes I do PP.

I was diagnosed last week. But I'd guess I've had it a good 4-5 years. My fatigue is just off the scale and sometimes too fatigued to sleep. Currently my pain is at least 15/10. My quads are so painful and tender I didn't know my quads could feel pain, they've never been like this. I would say my bum cheeks are so sore and tender but I know most are very delicate here so won't mention that. But think a three hour squash match when you've not played for a month. I'm trying to be positive. I was thinking a good massage would sort my legs out but if you say no I'll listen to you. Any sources of info you can suggest will help. I watched a video Saturday and they suggested a restricted diet. When I say restricted I might as well die, no dairy, no meat, no carbs, very restricted list of veggies. As bad as my pain is going into a British winter with such a small amount of food NO. Perhaps if it was the summer at the caravan with fresh fish and salads I could try. But with gusting swirling rain as we've had today nope need comforting food. I might change my mind about this when the pain flairs.
 
Anyone hear that Dale had a freebie to try?

I think I know the BA but never heard her soeak English only Welsh and she sounds so different.

She has some vids on YT, but now and again throws a tough one in, which I might or might not have done.
 
I was diagnosed last week. But I'd guess I've had it a good 4-5 years. My fatigue is just off the scale and sometimes too fatigued to sleep. Currently my pain is at least 15/10. My quads are so painful and tender I didn't know my quads could feel pain, they've never been like this. I would say my bum cheeks are so sore and tender but I know most are very delicate here so won't mention that. But think a three hour squash match when you've not played for a month. I'm trying to be positive. I was thinking a good massage would sort my legs out but if you say no I'll listen to you. Any sources of info you can suggest will help. I watched a video Saturday and they suggested a restricted diet. When I say restricted I might as well die, no dairy, no meat, no carbs, very restricted list of veggies. As bad as my pain is going into a British winter with such a small amount of food NO. Perhaps if it was the summer at the caravan with fresh fish and salads I could try. But with gusting swirling rain as we've had today nope need comforting food. I might change my mind about this when the pain flairs.
Penny that sounds horrendous. Why has it taken so long for you to receive a diagnosis? Do you know what's caused the condition? Sorry for being so personal & I'll understand if you don't want to reply.
 
Sorry to hear your story PP. Its between a rock and a hard place getting any relief and its a case of trial

and error and having a good GP who will refer you to a rheumatologist. Then thats just the beginning.
 
Penny that sounds horrendous. Why has it taken so long for you to receive a diagnosis? Do you know what's caused the condition? Sorry for being so personal & I'll understand if you don't want to reply.


I had a head injury Jan 2014 and whilst the bump itself was not a major head injury ie I'm alive, no blood, no bones sticking out I have a huge (20+) range of symptoms. Pain, tremors, shaking, always chuffing freezing, lots of pain, headaches, from the 41 symptoms I score 19, about 3 I'd say half but five of them mega. Of the test which is part 1 and 2a +2b. Overall I scored about 16/19 and 10/12, so it's pretty conclusive. Minimum scores were 7+5, but as my scores were high.

Ive had crap doctors. Some of the favourite comments have been,
It's your age
Learn to live with it
The pain is not real
Being sent for test that have never existed for what I had.
I wish I could sleep for 11 hours.
I've never heard of that as a symptom.
When I said I had difficulty with Welsh grammar I was told "so you speak English". So what I'm bilingual always have been, to ignore half of my language, my culture, etc. I'll leave it to your imagination my reaction.

Because I've complained that doctors are crap they discharge me. It took over 10 doctors to diagnose my vertigo, that included 3 neurologists and 2 GPs with special interests with ENT. I said from the start that there was something odd with the balance semicircular things and that took 3 consultants, plus 2 that specialised only with balance. Have to say 4 of that five were very good.

One doctor told me because I still had higher results for memory and other stuff she said she couldn't help. But if you knew where I started from....

Doctors have too much power to discharge you and that is it. This isn't the place to put all the gorey details vone had me down as a beauty therapist when I was a computer programmer. When I complained nobody did anything. The senior GP has proven to be less skilled than I gave him credit for. I hope to meet him when he's retired so I can give him my opinion. He's great to promise and the opposite to deliver.

I also have some Head Injury symptoms different to FM stuff.

I think I've not used words that doctors understand. So I said I've vibrations but they only understand shakes or tremors, there are just so many examples of that. I've said I feel full quickly after food but they only understand bloated. I've said huge discomfort they only register pain. Pre pandemic I went to see ond doc with a huge Oxford English Dictionary and told him the words I used were perfectly acceptable for my symptoms.

I'm not sure if I've answered the question but the whole thing is a mess it's difficult to know how to unpick it all.

Feel free to PM.
 

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