compression pump
I just found out my insurance is miraculously going to 100% cover a compression pump for me for the constant swelling in my ankles. (apparently lymphedema can occur anywhere after surgery).
I think it's called the FlexiTouch pump. Does anyone have any experience with this or any other pump?
Comments
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Hi pesky,
That's great news that your insurance will be covering this cost!
We're sure others with more knowledge on this type of pump will be by shortly to weigh in. In the meantime, we thought it might be helpful to share this page from the main Breastcancer.org site on Pneumatic Pumps for Lymphedema, to get a good understanding about how these devices work.
We hope this helps and that you find your pump helpful!
--The Mods
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I got my Flexitouch pump for my arm a month ago. It is great having it at home and able to use it daily instead of having to go to PT 1-2 times a week. I hope yours is successful for you.
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I love my flexitouch, have used it about a year now. I no longer have to use it as frequently as Idid in the beginning. My arm and torso lymphedema responded right away. I wish you the same success!
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Thank you for the replies! I will be honest, I'm mostly looking forward to not having to drive the 35 minutes to PT all the time.
My issue is mainly in my ankles so I think I'm getting one that covers my torso and legs. My PT is working with the FlexiTouch folks to set up a time for them to come to one of my PT appointments so I can try it out and make sure it's something I will be okay using at home, and then after that I'll just use that and not have to go to PT anymore.
I've only had 3 appointments so far with PT, but don't see any difference at all from it. I'm hoping using the pump daily will be beneficial, in addition to continuing to use my compression stockings, which were super expensive and only help minimally. Elevating my legs does absolutely nothing for me.
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Hi ladies,
My name is Crystal and it wasn't until this blog that educated me about lymphedema that I was able to talk to my doc about it with my arm about I was feeling and he agreed and prescribed therapy and the compression sleeves. But I could never get my stomach to feel right after my diep flap surgery (6/3/19) or the lipo (9/3/19) procedure for fat grafting. I didnt have a flat stomach but now my arm, breast and stomach feel bloated and tight. I'm pretty miserable--°and my PT lymphedema specialist just resign. So I'm asking your opinions on the compression garment for the torso? I want to bring it up to my doc.
BC is the gift that keeps giving doesn't it 😔
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cwins1218, I got the torso part of the FlexiTouch Plus free and I use it along with the leg compression. I don't have the lymphadema tightness in my abdomen so I can't really say, but I will say that the pump is easy to use and is working well for my legs. They just measured me again and I lost a full centimeter in my ankles after 10 weeks of use. Not great, but not bad.
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cwins - since you had a DIEP surgery, I'd be sure to clear a pump for your torso with your docs.
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Thank you both! I had an appointment and told them about the machine and also getting a new lymphedema specialist. This site is my saving grace
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Pesky904, If I may ask, which company do you have for your primary insurance? I had a Flexi years ago and it really was difficult to use. I'm pretty confident things have progressed over the years and would love to try again! I hope you are comfy in sharing this info!
Thank you! Katie Jane
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Please my flexitouch pneumatic pump doesn't pump the lower half of the breast where the swelling is more concentrated neither does it pump the axilla. I have trunk and upper limb garment. The trunk is working fine even though I noticed that it works more on the groin of the unaffected side than that of the affected side. The chest garment is always hard to put on for it to lay flat on the shoulder and touch the upper chest. I don't want the unaffected breast to be pumped but that's what the pump does. Two trainers from the company tried to help set it up but I know something still isn't right. I called the helpline but nothing came out of it. Please any suggestion to make it work on my breast and for it not to stimulate the normal breast? I watched videos about how to put it on but the garments used in the demos doesn't look exactly like mine.
Thank you.
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Hello,
I am wondering if anyone has had success using the Flexi pump for breast edema, post-lumpectomy? Massage techniques did not work for me, even after strict usage, doing it daily. I do have the pump, and I was also fortunate to have my insurance pay for it. I have only used it twice, so far, so I’m wondering if anyone has had success reducing the inflammation and pain.
Thanks!
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I got mine in Feb 2020. I too have had so complaints and they tried to fix it by sending me a vest which is better than the arm-chest garment that I was using before. There are still some issues even with that, it still cannot massage the lower breast region where my swelling are located. I did it lying down to see if it will be better, but it's not. The vest did a better job however. So I have come to conclude that it's for daily maintenance to keep it from progressing. If you have significant pain and noticeable swelling, you still need to see your LE Therapist, once it's controlled, then you can go back to daily maintenance. Flexitouch is better than nothing. So I use the vest for my chest, then use the arm-chest garment for my arm, forearm, and fingers. At the moment, I am having a flare, so I'm seeing the therapist. Hope this answers a bit of your questions. Do stay safe.
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Hi MsPrecious
You wrote about a vest, is it this type ? bottom of the page for head and neck https://www.tactilemedical.com/products/flexitouch...
My PT recommended a pump and Tactile Medical told me to get the Entre system which only works on the arm, forearm and fingers, but I felt my breast is swollen. Hoping to get something also works on the breast. I am too scared to go to the PT.
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Yes ma'am. That is the vest and I also have the upper arm and core garments that I use for my arm, forearm and fingers. Take whatever garments you are given and your PT knows what to prescribe for the breast swelling.
My PT has been using an instrument on me that works so well. Basically what it does is that it pinches a small portion of the skin at a time, more like pulling up the skin to aid movement of the lymph underneath. It works like magic. Usually I see her once a week and I'm able to maintain it with flexitouch pump until the next appointment. I did missed a day or two of flexitouch and I am still fine by the time I go for my next appointment. She called the instrument lymphitouch (I don't know the spelling) and it's old name was physiotherapy touch. She said it's made in Finland. You can ask if your PT has it. My former PT didn't have it.
Hope this helps.
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Thank you. I went back to my PT this week after stopping for nearly three months. She said she is going to talk to Tactile Medical to get the Flexitouch. Will see how it goes.
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I started using a "Sequential Circulator" for the Right arm at home. Now looking for how to self measure since I probably will not be seeing the therapist as frequently ,since she thinks I am am managing it well, even though it goes up and down . I usedtodo manual massage 2x/day, and need to get back to that.
Has anyone found a "user friendly" measuring tape to help with self-monitoring? I find perception unreliable. My left hand is just too clumsy to measure the right arm. I see some tapes measures on amazon geared towards body builders that let you snap the end into a lock. They are cheap, but maybe an answer. Probably won't see the therapist as often . Any experience out there with laser therapy or surgical node transfer? Are they just temporary relief? I think there is more than one forum for lymphedema, so might post this on those as well.
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I just found out I can get a new flexitouch garment at no cost because warranty garment is 5 yrs.
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Castigame - Good news that it is no cost to you. Expecting my new pump system, Tactile Flexitouch today. Decided to go ahead and purchase since I met deductables/catostrophic, even though I will only pay 15%of cost, it is spendy. If I waited till next year and had to pay almost full cost, I do not think I could afford it. I have not tried self measure with the myotape yet. This article suggest that self measure is not accurate as perometer. But I think I am more interested in general monitoring rather than actual numbers, because I find self perception unreliable.
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