June 2017 Mental Health Awareness

Special days & weeks in June

Along with Advocacy & Awareness
for mental health related issues
(and a calendar for the month!)

by Madelyn Griffith-Haynie, CTP, CMC, ACT, MCC, SCAC
Part of the ADD/ADHD Cormidities series

JUNE is PTSD Awareness Month —
June begins with Sleep Disorder Awareness Week
and National Cancer Survivor’s Day

Online Marketing Gurus extol the effectiveness of piggy-backing posts onto particular events – how about one or several of the ones below?
They make GREAT, positive writing prompts!

Mark your blogging calendars!

Many days of the year have been set aside every month to promote awareness or advocacy of an issue, illness, disability, or special-needs related cause.

In addition to a calendar for the current month, each Awareness post attempts to offer a list highlighting important days and weeks that impact and intersect with mental health challenges — reminders for health problems that intersect, exacerbate or create additional problems with cognition, mood, memory, follow-through and attention management.

If I’ve missed anything, please let me know in a comment so that I can add it to the list below.

I pray that 2017 will be the year
when EVERYONE becomes aware of
the crying need for upgraded mental health Awareness —

Stay tuned for more articles about Executive Functioning struggles and management throughout the year (and check out the Related Posts for a great many already published).

Remember: If you write (or have written) an article that adds content to any of these categories,
feel free to leave a link in the comment section and I will add it to the post’s Related Content.

IMPORTANT: All links were active at the time I created this document, and I tried to limit the number of “.gov” sites and sites with federally funded content.

Since the American president is busily removing government content that doesn’t support his agenda, I can’t promise that off-site links will still be active when you click – or how much of the original content will remain.

Don’t forget that you can always check out the sidebar
for a reminder of how links work on this site, they’re subtle ==>

Awareness and Advocacy Events for June
(intersecting with Mental Health & cognitive challenges)

PTSD Awareness Month
Post-traumatic Stress Awareness-American Psychological Association
Symptoms of PTSD ADAA  (Anxiety & Depression Association of America)

Starting in 2010, Congress named June 27th PTSD Awareness DAY
(S. Res. 455).

In 2014, the Senate designated the full month of June for National PTSD Awareness (S. Res. 481). Efforts continue to honor this designation in the coming years.

Related Posts:
PTSD Overview – Awareness Post 2016
C-PTSD: Complex PTSD Awareness
When Fear Becomes Entrenched & Chronic

LinkList: PTSD & TBI too Articles & Supports

National Brain Injury Awareness Month (Canada)
The Brain Injury Association of Canada

Related Posts:
How do brains get damaged? Is yours?
TBI Recovery – like life on the high seas

LinkList: PTSD & TBI too Articles & Supports


National Aphasia Awareness Month
The National Aphasia Association

Aphasia is more common than Parkinson’s Disease, cerebral palsy or muscular dystrophy. Nearly 180,000 Americans acquire Aphasia every year and affects about two million Americans alone. However, most people have never heard of it.

Aphasia is an acquired communication disorder that impairs a person’s ability to process language.

It does not affect intelligence — it impairs the ability to speak and understand others, and most people with aphasia experience difficulty reading and writing.  The diagnosis does NOT imply a person has a mental illness.

The most common cause of aphasia is stroke (25-40% of stroke survivors acquire aphasia). It can also result from head injury, brain tumor or other neurological causes.

If the symptoms of aphasia last longer than two or three months after a stroke, a complete recovery is unlikely, yet some people continue to improve over a period of years and even decades. Improvement is a slow process that usually involves helping the individual and loved ones understand aphasia as well as learning compensatory strategies for communicating.

National Congenital Cytomegalovirus Awareness Month
The CMV Action Network

ONLY 9% of women know about CMV.

ANYONE and EVERYONE of child-bearing age needs to click the link above to learn what you need to do to protect yourself so you protect your unborn child from potentially devastating mental & physical disorders.

Sleep Disorders Awareness Week
June 1-7
American Sleep Association
American Academy of Sleep Medicine
Circadian Sleep Disorders Network

Related Posts:
*  An Open Letter to Sleep Sites EVERYWHERE —
Asking for a Legitimate Place at the Table

*  Sleeping with the Enemy: Mom’s N-24
*  Up all Nite – Sleep away the Day?

LinkList: ALL Sleep Disorders Articles

Down’s Syndrome Awareness Week (UK)
June 4-10
Down’s Syndrome Association

Related Post: World’s First Down’s Syndrome Zumba Instructor

30th Annual National Cancer Survivors Day
Sunday, June 4th, 2017  (First Sunday in June)
The Official Website: National Cancer Survivors Day
Improving Cancer Survivors’ Mental Health

As a melanoma survivor myself  — several decades clear now and one of America’s more than 15.5 million cancer survivors — this is indeed a day to celebrate (and pray that lives & research funding will NOT fall victim to short-sighted budget cuts)


World Sickle Cell Day
June 19
Sickle Cell Disease Awareness

It is not just about Race; it’s also about Region. 

Sickle Cell Disease [SCD] is now believed to be a “tropical disease” where the red blood cells mutated to protect the body from Faliciparum Malaria. It is the most frequently occurring genetic disease on earth.

In the United States, 1 out of 10 African Americans have sickle cell trait and 1 out of 625 newborns have the disease.

Individuals with sickle cell trait (AS) inherit one gene for normal hemoglobin (A) and one gene for sickle hemoglobin (S) – carriers of the disease but usually free of medical problems.

Individuals with sickle cell disease (SS) inherit two genes for sickle hemoglobin (S), symptomatic because their red blood cells do not make normal hemoglobin.

Contrary to what you may have heard, sickle cell is NOT confined to African Americans. Within the United States SCD currently affects more people of African descent, but the gene can be found in in many nationalities:

Arabs, Greeks, Italians, Latin Americans, Native Americans, people from India as well as Caucasians — and the facts are being updated world wide.

All races should be screened for this hemoglobin at birth.

Globally, millions of people of every race have Sickle Cell Trait — and about 2 million people have sickle cell trait in the US alone.  There is significant concern about the effects of sickle cell trait as it relates several known situations.

Research has shown that those who carry the SC trait:

* who become overly fatigued and/or dehydrated in extremely hot temperatures are at risk of death, especially athletes;

* who visit high elevations are risking damage to their eyes necessitating eye surgery and resulting in partial to full blindness.

Finally, Pulmonary Hypertension is now being looked at as an issue not only for SCD patients but for any who have the trait.

Click HERE for a great deal more information.

© 2017, all rights reserved
Check bottom of Home/New to find out the “sharing rules”
(reblogs always okay, and much appreciated)

Other links to other posts and lists can be found below (in the Related Content section at the bottom of the majority of my articles), with my appreciation for improving your own Awareness, with hopes that you will help me SPREAD THE WORD!

Thanks again to Terri Mauro, Parenting Special Needs Expert from the VeryWell.com site
for many of the links that formed the genesis of the original Awareness articles.

As always, if you want notification of new articles in this Series – or any new posts on this blog – give your email address to the nice form on the top of the skinny column to the right. (You only have to do this once, so if you’ve already asked for notification about a prior series, you’re covered for this one too). STRICT No Spam Policy

IN ANY CASE, do stay tuned.
There’s a lot to know, a lot here already, and a lot more to come – in this Series and in others.
Get it here while it’s still free for the taking.

Want to work directly with me? If you’d like some coaching help with anything that came up while you were reading this Series (one-on-one couples or group), click HERE for Brain-based Coaching with mgh, with a contact form at its end (or click the E-me link on the menubar at the top of every page). Fill out the form, submit, and an email SOS is on its way to me; we’ll schedule a call to talk about what you need. I’ll get back to you ASAP (accent on the “P”ossible!)

You might also be interested in some of the following articles
available right now – on this site and elsewhere.

For links in context: run your cursor over the article above and the dark grey links will turn dark red;
(subtle, so they don’t pull focus while you read, but you can find them to click when you’re ready for them)
— and check out the links to other Related Content in each of the articles themselves —

Related articles right here on ADDandSoMuchMore.com

Related Content ’round the ‘net

BY THE WAY: Since ADDandSoMuchMore.com is an Evergreen site, I revisit all my content periodically to update links — when you link back, like, follow or comment, you STAY on the page. When you do not, you run a high risk of getting replaced by a site with a more generous come-from.

About Madelyn Griffith-Haynie, MCC, SCAC
Award-winning ADD Coach Training Field founder; ADD Coaching field co-founder; [life] Coaching pioneer -- Neurodiversity Advocate, Coach, Mentor & Poster Girl -- Multi-Certified -- 25 years working with EFD [Executive Functioning disorders] and struggles in hundreds of people from all walks of life. I developed and delivered the world's first ADD-specific coach training curriculum: multi-year, brain-based, and ICF Certification tracked. In addition to my expertise in ADD/EF Systems Development Coaching, I am known for training and mentoring globally well-informed ADD Coach LEADERS with the vision to innovate, many of the most visible, knowledgeable and successful ADD Coaches in the field today (several of whom now deliver highly visible ADD coach trainings themselves). For almost a decade, I personally sponsored and facilitated seven monthly, virtual and global, no-charge support and information groups The ADD Hours™ - including The ADD Expert Speakers Series, hosting well-known ADD Professionals who were generous with their information and expertise, joining me in my belief that "It takes a village to educate a world." I am committed to being a thorn in the side of ADD-ignorance in service of changing the way neurodiversity is thought about and treated - seeing "a world that works for everyone" in my lifetime. Get in touch when you're ready to have a life that works BECAUSE of who you are, building on strengths to step off that frustrating treadmill "when 'wanting to' just doesn't get it DONE!"

45 Responses to June 2017 Mental Health Awareness

  1. Pingback: Sleep Awareness and Health | ADD . . . and-so-much-more

  2. dgkaye says:

    Always sharing your informative posts Madelyn. 🙂 xx

    Liked by 1 person

  3. Pingback: Executive Functioning & Diseases of Aging | ADD . . . and-so-much-more

  4. Pingback: Surviving Cancer – a celebration | ADD . . . and-so-much-more

  5. Wendy says:

    I love that you do this. I learn so much, every month. I have been remiss in writing posts about events. Long story. Having a hard time writing.
    As always I’m glad I found you tonight. ♡♡


  6. TT says:

    Reblogged this on In through One door and out the other and commented:
    “Please share–it’s how ideas spread!” – Madelyn Griffith-Haynie


    • I love it when these monthly calendars are reblogged. In today’s world, where budgets are being “balanced” on the backs of the poor, the old, and the infirm, information and advocacy has never been more important. Research and clinical trials cost money, of course, but a sick populace costs more. Thanks so much for helping to spread the word.


  7. So many important topics to truly note and be aware of. As we step outside ourselves there is so much to be aware of.

    Liked by 1 person

  8. Liz says:

    Much appreciated and solely needed, this needs to be an open discussion at most work places really. So sad that most keep things secret. Love your movement.

    Liked by 1 person

    • Thanks, Liz. It’s really disturbing that it’s not at the forefront of the minds of our politicians, who have always been confoundedly short-sighted about medical research and the need for appropriations.

      Had Reagan listened to his Surgeon General and dedicated emergency research dollars instead of ignoring the emerging threat of an Aids epidemic, how many lives would have been spared?

      If Sickle Cell funding had been at effective levels MUCH earlier, it wouldn’t be news that transfusions and gene therapy could save (and could have saved) millions from painful – and needless – deaths.

      Awareness and advocacy have never been more important, as America’s current president proposes to cut billions from health-related funding!

      Liked by 1 person

  9. -Eugenia says:

    Reblogged this on BrewNSpew and commented:
    Sharing useful information from Madelyn…

    Liked by 1 person

    • Thank you so much for the reblog, Eugenia.

      As they say, “An ounce of prevention is worth a pound of cure!” Research funding is prevention’s vaccination. Without widespread public awareness and advocacy, that vaccination will not be made available.

      We do what we CAN, right?


  10. -Eugenia says:

    Excellent information. Sharing.

    Liked by 1 person

  11. We need to keep this in the public eye so more can be done and more money made available.

    Liked by 1 person

    • ABSOLUTELY, Karen. Your comment is right on point. Thank you for taking the time to leave it.

      Liked by 1 person

      • I know first hand how the mental health team let people down due to funding cuts. Also the stigma that is still there. I have said all along it should not be called mental but head or mind health or something else.

        Liked by 1 person

        • And the attitude generated by budget cuts to the health sector seems to infect the care we DO receive — almost “why bother?”

          As for stigma — I have been doing “brain-based coaching” for almost 30 years now, and many of my coaching colleagues STILL fail to get it. Sad & discouraging – and harmful!

          I used to believe I’d see the end of stigma in my lifetime if enough of us put our shoulders to that wheel. Many days now I wonder if the world will EVER see it.

          Still, I do as much as I am able without funding of my own — and pray.

          Liked by 1 person

  12. Léa says:

    I shudder to think of the outcome of proposed healthcare changes in America. You know all too well that Mental Health issues will be buried in the avalanche.

    Liked by 1 person

    • Buried more deeply, that is. Mental Health issues have never really made it out of the black holes of the ignorance of years gone by.

      I shudder with you, Léa, and do what little I CAN to raise awareness, praying enough people will awaken and become part of the solution. THANKS for reading and ringing in.

      Liked by 1 person

  13. Lucy Brazier says:

    Thank you, as ever, for bringing these important subjects to the attention of the world! I really admire your tireless work for mental health, it is so very important and you are an angel. Sending big hugs.

    Liked by 1 person

  14. thanks for the information, I had no clue that so much events exist…

    Liked by 1 person

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