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Product Description

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ABOUT WALK•HERO COMFORT AND SUPPORT

WALK•HERO is the developer and manufacturer of a new insole technology that helps correct over pronation (also known as flat feet).

In the past year, we has helped change many of people’s lives with our insole, recently, we produced the latest series, more solid support!

ENHANCED PERFORMANCE

Our Multicolor Series shoe inserts offer the orthotic-grade arch support, yield maximum alignment of the ankle joint, and provide a stable foundation and alleviates discomfort caused by plantar fasciitis. It provides superior relief by redistributing pressure about the foot to minimize repetitive stresses with full-length, semi-rigid stability cradle. This means enhanced performance with more support, less stress, and fatigue.

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MOBILITY

Excellent mobility allow for free and easy movement of the foot, without locking it in place.

ALIGNMENT

When you step into the plantar fasciitis insoles, you are aligning your kinetic chain. Align the ankle into a more neutral position, providing stability, support, and comfort which allows you to move and feel best.

SUPPORT

Our orthotic inserts provide firm and resilient arch supports to the subtalar joint, guiding the foot through natural movement while preventing overpronation or supination.

CUSHIONING

The cushioning system of our shoe insert is integrated with sponge souffle foam base and EVA molded for contour, provides full length cushioning and comfort.

APPLICABILITY

Our orthotic inserts are suitable for wide shoes, such as sports shoes, work boots, etc.

Plantar Fasciitis Orthotics Arch Supports Inserts - Thin and Cus

CURRENT ISSUE
September, 2021

No. 106 (9)

2020 Impact Factor: 9.941 Submission > Acceptance: 52 days
ARTICLES IN THREE SENTENCES
Article

Long-term outcomes from the phase II L-MIND study of tafasitamab (MOR208) plus lenalidomide in patients with relapsed or refractory diffuse large B-cell lymphoma

This open-label, single-arm study investigated the long-term efficacy of tafasitamab plus lenalidomide in 81 patients with relapsed/refractory diffuse large B-cell lymphoma. The response rate was 57.5%, including complete responses in 40.0% of patients, and the median duration of response was 43.9 months. This treatment is a valuable option for patients not eligible for autologous stem-cell transplantation.

Johannes Duell et al.

Case Report

Clinical genomic profiling of novel grey zone lymphoma paired lesions with sequential central nervous system involvement in two adolescent patients

Grey zone lymphoma is a B-cell lymphoma, unclassifiable, with features intermediate between those of large B-cell lymphoma and classic Hodgkin lymphoma. The in-depth study of the two adolescent patients described in this case report expands the clinicopathological and genomic spectrum of this rare pediatric disease. Moreover, it provides information on their response to treatment.

Cagla Y. Benkli et al.

Article

CAMT-MPL: congenital amegakaryocytic thrombocytopenia caused by MPL mutations - heterogeneity of a monogenic disorder - a comprehensive analysis of 56 patients

The clinical picture of 56 patients with congenital amegakaryocytic thrombocytopenia due to MPL mutations was much more varied than previously thought. Twenty-five per cent of them had no signs of thrombocytopenia at birth, and 50% had non-hematologic defects. Pancytopenia developed in (nearly) all patients and hematopoietic stem-cell transplantation was effective in 87% of cases.

Manuela Germeshausen et al.

Article

Oxidative stress activates red cell adhesion to laminin in sickle cell disease

Sickle red blood cells exhibit abnormal adhesion to laminin mediated by Lu/BCAM protein at their surface. This study provides evidence of the involvement of oxidative stress in post-translational modifications of Lu/BCAM which impact the protein’s distribution and cis-interaction with glycophorin C at the cell surface activating its adhesive function in dense sickle red cells. The authors speculate that antioxidant drugs might attenuate this phenomenon.

Maria Alejandra Lizarralde-Iragorri et al.

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