Patient Choice

Patient Choice Patient Choice is an independent and impartial Dispensing Appliance Contractor for NHS prescriptions.

A wide range of medical appliances (including non-prescription products) are also available to purchase from Patient Choice Direct. Patient Choice has received start-up funding from the Big Lottery Fund via Big Venture Challenge and UnLtd the foundation for social entrepreneurs.

18/06/2026

“I knew something was seriously wrong.”

For years, Sherry lived with heavy, painful and swollen legs, while feeling self-conscious and dismissed when seeking answers.

Her story shows why lipoedema awareness matters, and why listening to patients is so important. 💛

You can watch and read Sherry's full story using the link in our bio. 🔗

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists.💛

17/06/2026

For Sherry, the signs of lipoedema started young, but it took decades to understand what was really happening.

Her story highlights the impact of living with undiagnosed lipoedema and why diagnosis and awareness matter so much. 💛

You can discover Sherry's story from the link in our bio. 🔗

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists.

Please share to raise awareness for lipoedema this June.💛

17/06/2026

Match day essentials, sorted.⚽

Whether you’re cheering from the sofa or heading out to watch the match, comfort is always part of the game plan.

You can see our range of compression hosiery at https://www.patientchoicedirect.com/ or go to the link in our bio. 🔗

15/06/2026

After living with lipoedema for 40 years, Sherry shares her journey to diagnosis, management and finding the support that helped her feel understood.💛

Her story is a powerful reminder that lipoedema is not your fault and that you are not alone.

Read and watch Sherry’s full story here: https://www.patientchoicedirect.com/sherry-s-lipoedema-story-40-years-of-lipoedema

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists. 💛

12/06/2026

After years of feeling alone, Dymphie found her confidence again. 🩷

Through the right compression, management and support, Dymphie was able to regain her confidence and even proudly shows off her compression tights.

Dymphie has ever so kindly shared her inspirational story, including key information on how she manages and supports her lipoedema.🩷

You can discover Dymphie's story from the link in our bio. 🔗

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists.

Please share to raise awareness for lipoedema this June.🩷

10/06/2026

Even after surgery, Dymphie faces a lifelong journey of managing lipoedema.

Dymphie has ever so kindly shared her inspirational story, including key information on how she manages and supports her lipoedema.🩷

You can discover Dymphie's story from the link in our bio. 🔗

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists.

Please share to raise awareness for lipoedema this June.🩷

✨ Patient Choice is proud to be supporting the Lymphoedema support network (LSN) roadshow in Derby.✨The upcoming LSN...
10/06/2026

✨ Patient Choice is proud to be supporting the Lymphoedema support network (LSN) roadshow in Derby.✨

The upcoming LSN roadshow will be held at the Museum of Making, Derby, on Monday 22nd June (10am–4pm) and we're delighted to be attending!

This fantastic event brings together people living with lymphoedema, healthcare professionals, and industry experts for a day of learning, support and shared experiences. Attendees will hear from leading specialists, connect with others in the lymphoedema community and explore the latest products and services available.

Come and visit the Patient Choice team - we'd love to meet you and chat about how we're supporting patients living with lymphoedema. 🩵

To book your place (£10 per person), please email [email protected] or phone 0207 351 0990.

09/06/2026

After years of living with swollen, painful legs, Dymphie’s journey led her to a diagnosis of lipoedema and varicose veins. Then, a search for the right support, treatment and compression.

Her story is a powerful reminder that being heard, understood and supported can make all the difference.

Read and watch Dymphie’s full story here: https://www.patientchoicedirect.com/dymphie-s-story

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists. 🩷

05/06/2026

When Hannah began to research Lipoedema, there wasn't much support in the UK. Hannah's story echoes the importance of awareness and how education is a crucial part of living well with lipoedema. 🧡

You can discover Hannah's story from the link in our bio. 🔗

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists.

Please share to raise awareness for lipoedema this June.🧡

04/06/2026

Lipoedema led Hannah into a cycle of dieting and unhealthy restriction, even sometimes making her sick. Her story is one of resilience that brings light to just how much lipoedema can affect people in so many different ways. 🧡

You can discover Hannah's story from the link in our bio. 🔗

This Lipoedema Awareness Month, we're sharing the real experiences of those living with lipoedema and raising awareness for a condition that affects so many globally, many of whom are unaware that it even exists.

Please share to raise awareness for lipoedema this June.🧡

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Wellington
TA219FN

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