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Non-surgical breast lift and enlargement

There are some alternatives to having a breast lift implant or breast enlargement implant surgery for someone wishing to lift or increase the size of breasts:


Brava Breast Enlargement Shaping System
The Brava Breast Enlargement Shaping System uses a tissue expansion technique popular with medical professionals for 30 years.  It works by placing a gentle amount of tension (a 3-dimensional pull) on the breasts to allow new breast tissue to grow.  With the BRAVA Breast Enlargement and Shaping System women can expect to achieve an increase in breast volume from 35cc to 250cc of lasting tissue growth, different to simply using a breast pump to increase the size of the breasts because tension placed on the breasts actually helps breast tissue to grow.  It costs around 25%-30% of the average cost of breast augmentation.

Breast Pumps
Breast Pumps are a popular and natural way to enlarge the breasts (also used by mothers to extract milk) and there are a number of available pumps, from hand held manual pumps to battery (or AC) operated.  Breast pumps work by creating a vacuum around the breast that pulls body fluids into the breast tissue, thereby enlarging the breasts.  The result of the pumping makes the breasts larger and firmer but the breasts will eventually return to their former size unless the pump is used on a regular basis.


Breast Feather Lift (APTOS® procedure)
The Breast Feather Lift is an alternative to a breast lift implant. It uses the APTOS® procedure: biocompatible barbed threads are used to lift the breast with no visible scarring. The Breast Feather Lift works to help breasts with moderate droop to uplift and correct asymmetry.
Aptos® threads are inserted under the skin at different angles using an adapted hypodermic needle, which leaves only tiny entry and exit marks that heal quickly. The threads are then activated to lift the excess skin leaving no scarring as the skin is literally pulled tighter using threads which are invisible under the skin.


Aptos® procedure involves minimal discomfort, no scars, and quick recovery as one may return to work in less than a week. The Aptos® lift procedure is safe, quick and easy to perform. Aptos® lift is performed under local anesthesia using a very thin needle. The Aptos® threads are inserted into the subcutaneous fat, at a required depth, along the contours that were previously marked.


Since no skin is removed and no incisions are made, this Aptos® lift technique is not advantageous for people with excess skin.

Caci Bust Treatment
The Caci Bust Treatment helps lift, tone and strengthen, muscles around the bust area, and is another alternative to a breast lift implant.  Apparently, after just one session patients experience a “lift” for up to five days.  This treatment is available at beauty treatment centers.
The CACI Bust Treatment uses a machine originally developed to treat muscle injuries, but it can create a half-inch lift on each breast. The machine sends out electrical impulses which cause muscles to clench, strengthening and lifting. The treatment could be painful for candidates having sensitive breasts. A course of ten treatments is recommended.

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  • According to the results of a pilot trial published early online in the Lancet Neurology, early intensive lowering of blood pressure after acute intracerebral haemorrhage (ICH) is clinically feasible and warrants further investigation in a large, randomised trial. This study was conducted as a run in to a larger clinical trial, and involved over 400 patients with acute ICH who had elevated systolic blood pressure (150-200mmHg). All had been diagnosed by CT within six hours of symptom onset, and had no known definite indications or contra-indications to treatment. They were randomised to intensive lowering of blood pressure to a target systolic of 140mmHg (n=203) or to standard management (target systolic 180mmHg; n=201). The primary efficacy endpoint was the proportional change in haematoma volume at 24 hours. The main findings were as follows: • At 24 hours, the mean proportional haematoma growth was 36.3% in the guideline group and 13.7% in the intensive group (difference 22.6%, 95% CI 0.6–44.5%; p=0.04). After adjustment for initial haematoma volume and time from onset to CT, the inter-group difference was no longer statistically significant (p=0.06) • The absolute difference in haematoma volume was 1.7mL (95% CI -0.5 to 3.9; p=0.13). • From randomisation to 1 h, mean systolic BP was 153 mmHg in the intensive group and 167 mmHg in the standard group (inter-group difference of 13.3 mmHg, 95% CI 8.9–17.6 mmHg; p<0.0001) • Between 1 and 24 hours, the mean systolic BP was 146 mmHg in the intensive group and 157 mmHg in the guideline group (inter-group difference of 10.8 mmHg, 95% CI 7.7–13.9 mmHg; p<0.0001). The authors conclude that a large randomised trial is needed to define the effects of early intensive BP-lowering treatment on clinical outcomes across a broad range of patients with ICH. [Editor’s note: this summary was taken from the abstract, which did not contain any details of the drug regimens used.]

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