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Bring Depression into the Light
BlogMental HealthVolunteer Bloggers

Bring Depression into the Light

In today’s blog post our guest blogger, Stacey Mensah, discusses depression and very powerfully shares her personal experience with us. Get involved in the discussion and please do leave a comment below for Stacey.

Today’s blog post comes in somewhat of a sombre note. The topic we’ll be discussing is mental health, but more specifically depression. Many see this as simply a word, unable to comprehend the intensity of such a thing. Some, ​however, have experienced the feelings of hopelessness and darkness that come with this condition. Depression, whatever that may look like is real, you may not be able to understand it but it’s there lurking in the background. Coming from an African family but also a Christian one, my perception of mental health has always been an interesting one; and when I had depression as a child my mother was not quite convinced. In this blog post, I’ll be sharing with you, my experience of depression and my mother’s perception of it and what we have both learned from the experience.

The World Health Organization defines mental health ‘as a state of well-being; of complete physical, mental and social well-being and not merely the absence of disease or infirmity.’ Going on from this, depression can be understood as a persistent feeling of sadness and loss of interest. This typically affects how you think, feel and behave. This could lead to a variety of emotional and physical problems. This topic has always been of great importance to me not only because I’ve experienced this, but as a society, I feel like it’s so easy to focus on the outward appearance. If you’re smiling, then everything must be ok – surely. If you ask someone how they’re doing and they reply with, ‘I’m fine’, then all must be well. I have found that in the past this has not been the case at all. Anyone who has been around me for an extended period of time will know that I have a tendency to frequently ask the questions – How are you feeling? What are you thinking? How do you feel about that? And no, this is not because I’m a maniac who wants to get inside your head. It’s because I know it’s far too easy to hide your negative emotions and to some, in the end, this does become destructive.

I experienced depression from the age of 11 until the age of 20. I know I don’t have the condition anymore as I don’t have that persistent feeling of sadness. Although I do realise that depression does not have an expiry date, everyone does experience it differently. This post is not about telling you how we all experience the condition but rather encouraging you all to not be so eager when it comes to labelling or formulating certain medical conditions. One size does not fit all. During this period, I experienced intense feelings of loneliness, rejection and just overall darkness. The interesting thing however is that though I have always had my family around me, but that didn’t matter at the time. I was mostly inwardly focused, focusing on my own feelings – exaggerating my feelings of negativity and isolating and marginalising my positive emotions. They did not matter. I would always focus on the negative. This would be accompanied by 3 am phone calls to family members about how everything I did in my life was so wrong. The more than occasional bursts of tears would follow and just general misery. Although I was deep in the pits of depression I never did seek professional help. I didn’t want to be labelled as damaged or different. This was, of course, to do with the stigma of depression in society. I can talk about it now because I can look back at that time and think wow. I’m glad I went through that because it made me a stronger person and I’m able to empathise with people with mental health issues. It also brought my mother and me​ together. Here is what she had to say:

‘When you had depression, honestly, I felt helpless. I didn’t know what to do. I was always worried about what you were going to do as you were quite unpredictable. The only thing I could do was pray for you and answer those 3 am phone calls. Although you do mean everything to me, I had to understand that there was only so much I could for you. At the beginning, it was incredibly difficult as I just thought you were being dramatic and didn’t want to be put into certain social situations. After a while, though I learned to listen to you and from there we just had to work through it together.’

To describe depression as being a rough journey would be an understatement. It’s not easy. Some people have to seek medical help for it whereas others do not. Everyone is different. Families and cultures deal with it differently. The key thing that helped me during this time was having a strong support network – made of family and friends. What are your views on mental health? Comment down below or on our Facebook page and let’s open up the discussion.

See you soon x

***********************

The Lake Foundation would like to say a big thank you to Stacey for sharing her experience with depression, we hope that through her experience you have gained some insight into this condition.

For more information about depression you can visit Mind, Rethink Mental Illness and Croydon Drop In  

Out and About: Reducing Childhood Obesity Event in Croydon
BlogChildhood ObesityObesityUncategorized

Out and About: Reducing Childhood Obesity Event in Croydon

Over the past month or so we’ve had the opportunity to attend a number of interesting events to discuss a range of health issues and in today’s blog, we’ll give you a quick summary of a childhood obesity event we attended a few weeks ago.

Reducing Childhood Obesity

Childhood Obesity

On 18th January, we attended the Croydon Children, Young People and Families’ Network reducing childhood obesity event. This event brought together organisations in Croydon who are tackling childhood obesity to share experiences and also to understand Croydon’s new childhood obesity strategy.

The main speaker on the day was Bernadette Alves, Consultant in Public Health at Croydon Council, who took us through the Croydon Healthy Weight Action Plan for Children and Young People which aims to cover their plans from 2017 to 2020.

The Scale of the Problem

Bernadette Alves started by setting the scene with some background information stating that childhood obesity is a major priority for Croydon being one of their five main priorities for children in the borough. She explained that obesity causes children harm impacting their physical health, mental health, behaviour and day-to-day life (such as school attendance). She explained the extent of the problem telling us that 20.3% of children in reception (4-5-year-olds) are overweight or obese and 39% in year 6 (10-11-year-olds). When we look across the borough there is a lot of variation with Broad Green, New Addington, Selhurst and Thornton Heath having the highest levels of year 6 obesity levels and Sanderstead having the lowest year 6 obesity rate.

Croydon’s Action Plan for Childhood Obesity

We then heard how Croydon Council aims to tackle childhood obesity with their new strategy. Bernadette explained that their core priorities would be :

  • Sugar: to sign a sugar declaration and develop a borough wide sugar smart approach
  • Targeting and Integration: they will ensure that services are targeted to those most in need and develop an integrated interactive pathway of all services that are available to support children to reach and maintain a healthy weight
  • Physical activity: roll out the Daily Mile campaign to schools
  • Engagement of residents and the community: they will raise awareness of the impact of childhood obesity and support and empower residents to make behaviour changes.

The Council’s action plan, at the time, was in a draft phase and going forward they were conducting a consultation on the plan; the deadline for this was the end of January.  We also learnt that a Healthy Weight Steering Group was set up and is being led by Croydon Clinical Commissioning Group and Croydon Council; they will monitor the implementation of the action plan.

Unhealthy High Streets

Following Bernadette’s presentation there was time for questions and one of the issues raised was the large number of unhealthy takeaway restaurants in close proximity to schools.  In response to this Bernadette stated that there is a lot of work being conducted to create healthier high streets. She acknowledged that there is a major issue with fast food chains being placed near schools that target children with very cheap deals on their products.  Even data from the Royal Society of Public Health has shown that  Croydon has a particular problem with Central Parade in New Addington being the second most unhealthy high street in London.

Developing Better Relationships Between Local Government and Charities

Another issue that was raised during the Q&A was the lack of communication between small groups and the Council. It was felt that there needs to be a better working relationship between community groups and the Council that would enable all organisations working in this field to work effectively together, reduce duplication and align their objectives with the local approach. It was felt that the Council could provide more support to community organisations that goes beyond providing funding through their grants programmes but promoting projects and working in collaboration to ensure that projects are successful.

The event ended with a networking session where we could learn about the work being conducted by local community groups and charities.

This was a really interesting event and provided some good insight into local plans for tackling childhood obesity.

 

Fibroids Twitter Chat
FibroidsNews

Fibroids Twitter Chat

We are delighted to announce our next fibroids Twitter chat will be on  Wednesday 15th  February 2017 from 7pm-8pm. We will be joined by special guests Dr Sydney Dillard, CEO of Fighting Fibroids, Candice Bryan, CEO and Founder of Noire Wellness and Leah Salmon, Founder of the Naturally You Coach with host, our own Abi Begho, founder of The Lake Foundation.

This Twitter chat has been organised to allow for an in-depth discussion on fibroids, diet and exericse.

We’ll be putting questions to our expert panel and you can put your questions to them too. So if you have a burning question about fibroids or just want to get involved in the discussion then do join us on the day. To take part in the conversation please use the hashtag #FibroidsChat.

We look forward to tweeting with you!

We’ve Teamed Up With Voices for Autism
News

We’ve Teamed Up With Voices for Autism

We’re delighted to announce that we have teamed up with Voices for Autism to host our first Autism Health and Wellbeing Conference. This event is aimed at parents, carers and teachers of children with autism and will cover a range to topics to empower attendees with the information they need to successfully care for a child with autism.

On the day we’ll be looking at therapeutic options and the impact of nutrition and physical activity on autism. We’ll also explore autism friendly initiatives and hear personal stories from parents.

Autism is quite common in the UK affecting approximately 700,000 people. It is a lifelong developmental disability that affects how a person sees the world. It also affects how a person communicates with, and relates to other people. It is a spectrum condition which means people with autism have a range of difficulties in common but it affects everyone differently. It can be hard for those caring for a child with autism to find support and advice on how to manage their child’s condition and so organisations like Voices for Autism have been organising a range of much-needed support services.

Our conference aims to connect parents, experts, teachers and carers to create the perfect environment for shared learning.

This conference will be held on Saturday 15th July at the Bernard Weatherhill Community Space in Croydon. More details will be available from April 2017, but please save the date.

For more information please email events@thelakefoundation.com

Let’s Get Real About Dementia
BlogVolunteer Bloggers

Let’s Get Real About Dementia

In this week’s blog freelance journalist Stacey Mensah discusses dementia. 

Welcome back, you lovely people! It’s the end of another week and I don’t know about you but I’m glad it’s here. I’ve also just realized that it’s the last weekend in January! How are we feeling about that? I don’t know whether to be excited by the fact that we’ll be saying bye-bye to January blues, or sad because we are another month closer to bikini season – or should I say overall season. Ha! Let’s leave the issue of bikini season to one side – for now – and let’s discuss dementia, and how regular exercise can reduce the odds of developing this disease.

Dementia 101

Dementia refers to a set of symptoms that include, but are not limited to, memory loss and deficiencies with thinking, problem-solving and language. Although these changes are incredibly minor to start off with, over time they do become severe enough to affect everyday life. Of course, the best thing to do would be to get a proper assessment of problems but the waiting times of the NHS stretching as far as two weeks it’s best to take preventative measures while you still can.

In a recent study, it was found that people who exercised regularly appeared to have lower odds of developing dementia than those that didn’t.  This study followed more than 1,500 adults, aged 65 and older. This isn’t to say that if you’re younger than 65 you can stop reading – carry on, you’ll be surprised.

The symptoms of dementia can be seen in those that are younger than 65. This is usually referred to as having young-onset dementia. The stressful events of life including weddings, job losses and divorce have also been linked to this development. Unfortunately, there is a wider range of diseases that trigger young-onset dementia. Most importantly, people with this type of dementia are far more likely to be diagnosed with a rarer form of the disease. In both cases getting a diagnosis would be the best thing too – regardless of how long you may have to wait, it is worth it!

Getting Real

Here at the Lake Foundation, we take health incredibly seriously. It’s not a fad, but we do struggle. We are simply normal peopleand at times we have questionable eating habits. And of course when I say we, I mean me. Eating healthily and exercising regularly as always been an obstacle for me. Actually, to call it an obstacle would be a major understatement, as obstacles are usually overcome within time. This obstacle has become that piece of furniture in the corner that you just can’t seem to throw away. When you wake up, it’s there. When you go to bed, ooooh wait…no, ​it’s still there. When my family and friends ask me about it, I rationalize its being; somehow relating it back to the core of my existence. I know, how dramatic, right?

I tell you this because we are all in this together. For the start of February, my plan is to change the rules that I live by. For a wise woman once said that some rules are nothing but old habits that people are afraid to change.

Have a great weekend!

We’re Recruiting Volunteer Diabetes Community Champions
DiabetesNews

We’re Recruiting Volunteer Diabetes Community Champions

The Lake Foundation has teamed up with Diabetes UK to run a 12 month Diabetes Community Champion project in Croydon that is aimed at the African and African-Caribbean community.   Through this project we’re hoping to raise awareness of diabetes and how it can be prevented, and for those with diabetes, provide information on  how best to manage their condition and secure better health outcomes.

We’re currently looking for volunteers to take on the role of Diabetes Community Champions.

Diabetes Community Champions will raise awareness of diabetes and this may involve giving presentations, hosting information tables at events, distributing leaflets and information, taking part in local radio interviews, writing blogs and exploring creative ways of engaging with the black community.  In addition volunteers, if interested, can work with local GPs to identify pre-diabetics and work with them on a one-to-one basis to reduce their risk through a behaviour change programme.

Community Champions can dedicate as much time as they are able to this project, but ideally we’d like volunteers to commit to at least 1 – 2 days a month to ensure we can make the most impact possible.

Full training will be provided to all volunteers.

If you’re interested in being a Diabetes Community Champion, please complete an online registration form here or email info@thelakefoundation.com for more information.

The All-Party Parliamentary Group Asks for Written Evidence on Fibroids
FibroidsNews

The All-Party Parliamentary Group Asks for Written Evidence on Fibroids

The All-Party Parliamentary Group on Women’s Health is a cross-party group of MPs and Peers in the UK Parliament of Westminster. They have launched an inquiry into whether women are given an informed choice about the treatment options available for particular conditions. Fibroids and endometriosis are among the conditions the group would like to shine a spotlight on.

The group will produce a report which will assess if women are given an informed choice about treatment options and outline what improvements  need to be made.

As part of this inquiry the group is inviting interested parties to submit written evidence. Evidence can be submitted via the following links (endometriosis) (fibroids) or emailed directly to appgwh@mailpbconsulting.com using the pro forma below. Patient experience, anecdotal evidence as well as any sort of data would be gratefully received.

The group would like to hear about current practice as well as potential barriers and issues in order to understand what key recommendations the group can take forward. The group will be accepting written evidence until the end of February 2017.

If you’ve been affected by fibroids we strongly encourage you to submit written evidence on your experience when you were offered treatment. This will make a significant difference and help identify any issues that exist can be identified so that these can be addressed to ensure that the diagnosis and treatment pathway for all women is improved.

If you would like any further information about the inquiry or the group’s work more generally, please contact the group secretariat at appgwh@mailpbconsulting.com or call 020 7735 6963.

We Attended the Launch of Prostate Cancer UK’s Stronger Knowing More Campaign
BlogCancer

We Attended the Launch of Prostate Cancer UK’s Stronger Knowing More Campaign

Last week, we had the pleasure of attending the launch of Prostate Cancer UK’s Stronger Knowing More campaign. This campaign is aimed at black men and puts the spotlight on the fact that black men have a higher risk of developing prostate cancer. Black men have a 1 in 4 chance of developing prostate cancer, which is double the risk faced by white men.

The campaign was formally launched on 17th January at 15 Hatfields . The event started with a networking session where we were able to speak to staff members involved in developing this much-needed campaign, hear from men who have been affected by prostate cancer and view the very powerful images being used for Stronger Knowing More.

Powerful Imagery

Our first mission as we walked around the beautiful venue was to look at the exhibition of images which were created for the campaign.

Prostate Cancer UK worked with photographer Dennis Morris to create a collection of photographs of black men from the worlds of sport, politics and the arts as well as prostate cancer survivors in a show of strength against prostate cancer. The collection of images featured former WBA World Heavyweight champion David Haye, Olympic gold medallist, Linford Christie Labour MP, Chuka Umunna, writer and musician Benjamin Zephaniah, ex-England footballer Viv Anderson and Red Dwarf star Danny John-Jules.

Reading through the captions of the each picture was really inspiring, moving and empowering and we’re sure that as men see these it was make them reflect on their health and perceptions of prostate cancer.

It was also interesting to read the behind the scenes view of the creation of the pictures with photographer Dennis Morris explaining that each shot was carefully thought through. For his photo shoot he asked each of his subjects to select a location where they felt the strongest and he was able to capture moments of defiance, strength and vulnerability.  It is hoped that the pictures will tap into the inner strength of men and when combined with information will defeat the silence and stigma around prostate cancer.

Moving Stories

During the networking session we spoke to several men with experience of prostate cancer and were so moved by their experience and the fact that despite their health they were working tirelessly to raise awareness and support other men.  It was also interesting to learn of how some men came to be diagnosed, many by chance encounters with people who made them think which really highlighted that small gestures can make a huge difference in someone’s life.

We spoke to one man whose first words to us were: “that man saved my life” as he pointed to one of Prostate Cancer UK’s most well-known patient volunteers, Errol McKellar. He told us that he was waiting at a train station one day when Errol began speaking to him about prostate cancer and ended the conversation by giving him a leaflet, which he only took to “shut him up!” He said that leaflet stayed on his desk at work for two weeks and then during a slow day at work he read the leaflet and realised he had some of the symptoms of prostate cancer. He visited his GP and was later diagnosed with prostate c,ancer, which he said was devastating.  All he could think about was not being there for his wife and children and not being around to see his children grow up, “they are still so young”. Luckily he was diagnosed at a fairly early stage and his future is bright, but had he not met Errol McKellar his story could have been so different.

Inspiring Speeches

After the networking session it was time for speeches. We first heard from Tom Shrophire, Trustee of Prostate Cancer, UK who gave some background to the campaign and how it came into being. He said that there was a need to publically acknowledge the heightened risk black men have and start implementing a solution that seeks to raise awareness as many men don’t realise they are at an increased risk.  He said this work is part of Prostate Cancer UK’s aim to tame prostate cancer in the next 10 years and this means they have to make black men, black families and black communities a priority.

We also heard from Prostate Cancer UK ambassador, Errol McKellar, who shared his touching story about his experience with prostate cancer. He was diagnosed after reading a leaflet about the PSA test and then decided to have the test done. He explained how prostate cancer totally changed his life and was the most difficult challenge of his life. He described the importance of having a good support system and said he would have never made it through this disease without the support of his wife (“my wife was my strength”). He gave hope to men by saying his prostate cancer diagnosis had knocked him down, yes, but it hadn’t knocked him out.  He gave a realistic view telling the audience that he is still battling some of the side effects of treatment and of the disease itself and it has taken him a long time to come to terms with how it has affected his life.  He also described his more vulnerable moments, like when he was diagnosed, he said “he cried like a baby.”

We were so inspired by all the work Errol has done since his recovery.  After he recovered from his treatment and was fit to return to work he was contemplating how he could make difference. So he decided that he would speak to every man that came into his mechanic shop about prostate cancer.

On his first day back to work he started with his first customer and  asked him: “When last did you get your prostate checked?”  He then offered his customer a 20% discount if he got a PSA test done and reported back to him. Sure enough a few months later the man return for his 20% discount having completed his PSA test but was shockingly diagnosed with early stage prostate cancer. The man said that Errol should donate the discount to charity and keep raising awareness. That was back in 2011 and since then Errol has spoken to hundreds of men about prostate cancer which has resulted in 26 men being diagnosed with prostate cancer, sadly two of those men have since passed away.

Finally we heard from actor Rudolph Walker, who has been working with Prostate Cancer UK for a number of years to raise awareness. Whilst he hasn’t had prostate cancer himself he spoke of his close friend who sadly lost his life to prostate cancer, but had he known the symptoms and been diagnosed earlier he may still be here today.

Getting Involved

On the night Prostate Cancer UK asked us all to make a pledge to support their campaign and raise awareness and we’ve pledged to do just that.

You can also get involved in this campaign and Prostate Cancer UK have said you could do any of the following:

So let’s all get involved in raising awareness, breaking down the walls of silence and work towards saving our husbands, fathers, brothers, uncles, grandfathers, cousins and friends from prostate cancer.

Prostate Cancer UK’s Stronger Knowing More Campaign
CancerNews

Prostate Cancer UK’s Stronger Knowing More Campaign

This week Prostate Cancer UK launched their ‘Stronger Knowing More’ campaign which is aimed at black men and puts the spotlight on the fact that black men have a significantly higher risk of developing prostate cancer. Black men have a 1 in 4 chance of developing prostate cancer, which is double the risk faced by all men who have a 1 in 8 chance of developing prostate cancer.

In addition to this increased risk of developing this devastating disease black mean are twice as likely to die from prostate cancer.  Black men have a 1 in 12 lifetime risk of dying from prostate cancer whilst all men have a 1 in 24 lifetime risk of developing prostate.

As a result of these alarming statistics Prostate Cancer UK recognised the importance of ensuring that all black men are aware of their risk so they can take steps to do something about it.

Prostate Cancer UK’s Stronger Knowing More campaign uses positive and empowering portraits of black men from the worlds of sport, politics and the arts as a show of strength against prostate cancer. Former WBA World Heavyweight champion David Haye, Olympic gold medallist, Linford Christie and Labour MP, Chuka Umunna are among the well-known faces supporting this campaign.

Stronger Knowing More is calling on the black community to confront the increased risk of prostate cancer and break down longstanding taboos that have prevented black men from speaking about the disease.

It is not known why black men have an increased risk of developing prostate cancer but genetics is thought to play a role. We can all do something about this by being aware of the symptoms and men acting quickly and visiting their doctor, without delay, if they have symptoms they are concerned about.

For more information about black men’s risk of developing prostate cancer visit Prostate Cancer UK’s website here, view the video below or if you have any concerns you can call their helpline 0800 074 8383.

Did you miss our fibroids Twitter chat with Dr Sydney Dillard and Renee Brown Small?
BlogFibroids Twitter Chats

Did you miss our fibroids Twitter chat with Dr Sydney Dillard and Renee Brown Small?

Last night, we were so excited to host our first fibroids Twitter chat. We were joined by special guests Dr Sydney Dillard, CEO of Fighting Fibroids and Renee Brown Small Co-founder of The Fibroids Project with host, our own Abi Begho, founder of The Lake Foundation.

If you missed our Twitter chat you can check out our conversation below and look out for our next Twitter chat on Wednesday 15th February at 7pm (UK time).

Update June 2018: Please note that tweets from Renee Brown Small are no longer available so some information is missing from the chat below.