Listen "09: Margaret-Anne explains Lymphoedema and support"
Episode Synopsis
In this episode, we have such an interesting conversation with Margaret-Anne Garner, one of the lymphoedema specialists Lymphoedema Team.
Margaret-Anne gives us insight into her own career path and how she got into supporting people with Lymphoedema and Lipoedema, as well as explaining more about how to identify these conditions and support local people living with them.
As the only specialist #lymphoedema clinic in @NHSForthValley, if you’ve the condition, or know someone who may have, speak to us about possible treatment: [email protected] if you’ve any questions.
Information:
- Strathcarron's Lymphoedema and Lipoedema team: Lymphoedema Services | Strathcarron Hospice
- Join the Lymph Notes Choir: Join the Strathcarron Lymph Notes Choir | Strathcarron Hospice
- If you are a professional, you can also get in touch or refer: METLymphoedema Services | Strathcarron HospiceUPUK (start.page)
Thank you Margaret-Anne.
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By sharing people stories, we help to raise awareness of Strathcarron's services and impact, as well as to reduce the fear of Hospices and encourage more conversations about death and dying.
Hosted by Ailsa (from Communications) and Ross (from IT) sees us out and about, speaking to our own staff, as well as people living with life limiting conditions and the families they support.
We're nurses, doctors, social workers. We're volunteers, cleaners, cooks & therapists. We're fundraisers, administrators, accountants & physiotherapists. We will share their stories.
We also aim to ask and answer your questions.
The conversations we’ll have with our teams will be around their roles, impact and how each person supports people with life limiting conditions. We will also speak to volunteers, local organisations, fundraisers, schools - a whole host of people connected to the Hospice too.
If you have any questions re hospice or palliative care, Strathcarron Hospice, or would like to be on the Podcast, or have a story to tell, please get in touch via our email [email protected].
Margaret-Anne gives us insight into her own career path and how she got into supporting people with Lymphoedema and Lipoedema, as well as explaining more about how to identify these conditions and support local people living with them.
As the only specialist #lymphoedema clinic in @NHSForthValley, if you’ve the condition, or know someone who may have, speak to us about possible treatment: [email protected] if you’ve any questions.
Information:
- Strathcarron's Lymphoedema and Lipoedema team: Lymphoedema Services | Strathcarron Hospice
- Join the Lymph Notes Choir: Join the Strathcarron Lymph Notes Choir | Strathcarron Hospice
- If you are a professional, you can also get in touch or refer: METLymphoedema Services | Strathcarron HospiceUPUK (start.page)
Thank you Margaret-Anne.
======
By sharing people stories, we help to raise awareness of Strathcarron's services and impact, as well as to reduce the fear of Hospices and encourage more conversations about death and dying.
Hosted by Ailsa (from Communications) and Ross (from IT) sees us out and about, speaking to our own staff, as well as people living with life limiting conditions and the families they support.
We're nurses, doctors, social workers. We're volunteers, cleaners, cooks & therapists. We're fundraisers, administrators, accountants & physiotherapists. We will share their stories.
We also aim to ask and answer your questions.
The conversations we’ll have with our teams will be around their roles, impact and how each person supports people with life limiting conditions. We will also speak to volunteers, local organisations, fundraisers, schools - a whole host of people connected to the Hospice too.
If you have any questions re hospice or palliative care, Strathcarron Hospice, or would like to be on the Podcast, or have a story to tell, please get in touch via our email [email protected].
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