#ilnesses

[shuuenka]

WATERCOLOR PROJECT ~ Okita Souji + Anemone

But I must be cruel to be kind

Deep within a my head of stone

[ivanabajcer-blog]

“Sickness” (drawing,black ink,watercolor)

[diabetesyoyo]

Diabetic medicine should be free and available to everyone. Insulin, test strips and so on are saving our lives every day. Denying free access to them is inhumane. Shame on every government who does not give free diabetic care!

[longlivethereaper]

Guys

Guys

Sole survivors with

Hypo/Hyperthyroidism

Diabetes (type one or two)

Arthritis

Sciatica

Social Anxiety

Anxiety in general

Depression (and not just after they wake up, but like before hand.)

Chemical Depression

Eczema

Bad teeth

STRETCH MARKS

[pharmageek-lionelreichardt]

Invisible illnesses: what are you fighting for? #fsp15

  “I fight to get up in the morning, to hold my children in my arms, to go to a concert with a friend, to keep my relationships… I fight every day, an invisible yet oh so essential fight.”

What about you? If you’ve got an invisible illness, why do you fight?

This is the question being asked for the 14th week dedicated to invisible illnesses, which is focusing on the theme of the “invisible fight” and being shared on social media with the hashtag #invisibleFight.

  INVISIBLE ILLNESS #FSP15

The weight of the illness… the shock of the photos

Launched in 2002 in the United States, Invisible Illness Week continues to grow in the English-speaking world and on social networks each year in September.

In 2012, the organisation led its first photo campaign, which was republished on CNN’s website, and ever since then photography has played a central role in their campaigns.

So I want to show you some of the pictures I found on Twitter using #invisiblefight… plus some very touching messages, powerful struggles, personal accounts… and sometimes stories of suffering, too.

Discover snapshots of people’s lives and everyday struggles on Twitter now.

  To delve deeper, affected bloggers are invited to take part in the campaign by posting about their experiences of fighting illness.

  INVISIBLE ILLNESS #FSP15

These blogs also provide touching and heart-rending stories that shine a light on illnesses such as Alyson’s, a patient who suffers from a chronic illness and, through her blog, helps other women who, like her, are fighting illness.

  INVISIBLE ILLNESS Blog

Or like Lisa Douthit, a patient suffering from cancer and an auto-immune disease, a woman, mother, blogger and author of the book “Wellness warrior – Fighting for life in fabulous shoes”.

  INVISIBLE ILLNESS Blog

Invisible, silent, insidious… the exact wording doesn’t matter

A few days ago in Sanofi’s Public Health Forum group on LinkedIn, I wrote a post to share another campaign that is currently underway on social media: #sufferingthesilence.

    Sanofi Santé publique Forum

To break the silence around their illnesses (Lupus and Lyme Disease), Erica and Allie created their website Suffering the silence.

The site is first and foremost designed to create a community for patients and their loved ones.

A great initiative… and also very visual, with photos shared on Twitter using the hashtag #sufferingthesilence and patients taking selfies the way teenagers do (e.g. with their hand over their mouth) and with the name of their particular illness written on their arm… could this be about to go viral?

    #Suffering the silence

All of which continues the themes of Allie’s book, “Suffering the Silence: Chronic Lyme Disease in an Age of Denial”.

This is all very promising for the emergence of patient empowerment and for the voice of patients breaking the silence.

The silence will certainly be broken on Friday 2nd October at Sanofi’s Public Health Forum, which will be running all day at Sanofi France’s new head office in Gentilly.

Over 200 players in the healthcare sector are expected, for what promises to be an engaging programme, to discuss the complex issues caused by these diseases, and for which so much still needs to be done.

Two roundtables, speeches, presentations from startups and even true-story theatrical performances to put a spotlight on patients’ stories…you can find the full programme here.

You can also follow the day using the hashtag #fsp15 if you can’t attend in person.

Let me also remind you that if you’d like to join the group to discuss public health issues and the transformation of the healthcare system, you can join the LinkedIn group : 

  Sanofi Santé publique Forum

Let me just leave you with this final image that I found under the hashtag #invisiblefight.

Walt Disney Quote

The fight continues for everyone, by everyone, with everyone… to drown out the deafening silence that often reigns when it comes to illness.

  Digitally yours,

Lionel Reichardt – Pharmageek

Invisible illnesses: what are you fighting for? #fsp15 Invisible illnesses: what are you fighting for? #fsp15 “I fight to get up in the morning, to hold my children in my arms, to go to a concert with a friend, to keep my relationships...

[easybrothersforthewin]

im trying to not let my illness get the better of me as just wish to be able to get on with my life. I want to be able to go out and meet friends. I want to be able to film films. I want to be able to be able to do the things I love but I have to be careful as I know the slightest thing can make me worse. I cant afford to get any worse than I have as I know that will probably stick me in hospital. I would like to stay out of hospital but the fact that my illness conflict dont help.  I have been told i need to spend more time in the sun yet today when doing so I felt my blood pressure go funny when ever I wasnt in shade. I had an amazing day out but its been tough and tiring. Though what I dislike is that my mum sees me as some sort of supper woman, as I can still do things like go hang with my friends. I cant decide if and when my body get worse. I have no say over it despite the fact that I have been put on meds that are meant to help me get better. I had of known in advance that the weather was going to mess with my blood pressure or that my feet would end up really sore then maybe i would of rethought of going today. Though at the same time would of been stupid as i need to be out in the sun more and hadnt seen the friends i was seeing today for months. Im really trying to not let my illness get the better of me but im starting to reach a point where I no longer care about my health as no matter what I do nothing seems to get better and the people around me dont seem to care. it also doesnt help that I felt better before I got my diagnoses than after. im just trying so hard but im not sure what the point is anymore. 

[dirtydiana02]