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#ChronicIllnessVOICE Evening Edition: ~ a health newsletter for everyone! #notjustpatients #chronicillness| 01 July 2018

There are two special ‘Facebook frames’ that people can add to their profile pictures to wish the NHS a happy 70th birthday!
Find out more on the #NHS70 website: http://www.nhs70.nhs.uk/

A selection of online health related newspapers/magazines/newsletters/blogs/events

#notjustpatients



Did you know that you can join in on the celebrations on Facebook?

There are two special ‘Facebook frames’ that people can add to their profile pictures to wish the NHS a happy 70th birthday!

Find out more on the website:

 



Posts are Not in chronological order!

PLUS

Meditation 

KUNDALINI RISING || 432Hz Music to Balance Male Female Energy || Healing Music for Meditation | 5 February 2018

Meditative Mind  Published on 7 Jun 2018
It’s at the end!



 


FibroFlutters continuously

Advocating for a Multi-Disciplinary / Patientcentric approach to all aspects of medical healthcare. With a model approach using all the ‘stakeholders’ I’ve designed a patient’s perspective of what patient-centred care, patient-included, patient-involved, patient-centric should look like and involve, that’s everyone by the way! 

You all need to pitch in!!



 

Ronny Allan’s Latest Daily Newsletter via Nuzzel

Neuroendocrine Cancer Patient Voice and International Advocate. WEGO Health Patient Leader, Cure Today Contributor, Cancer Campaigner, Featured Blogger (@netcancerblog). Veteran.

Visit Ronny’s blog via this link >>>

Living with Neuroendocrine Cancer

 



 

Latest!

#alzheimers  #dementia  #care  

Alzheimer’s Reading Room Newsletter |  Bob De Marco| Headliner:  Dementia Care, Should A Caregiver be Truthful or Kind? | 26 June 2018

Also including  >>>

  • How to Use Bright Light to Improve Mood and Behavior in Alzheimer’s Patients 
  • Why the Eye Could be the Window to Brain Degeneration and Alzheimer’s Disease 
  • Alzheimer’s Reading Room Testimonials

and much more…


Why not subscribe to the AlzheimersReadingRoom.com. This is a free service. Join 40,000 active readers.
https://bit.ly/2M4G4cu

The Award Winning Alzheimer’s Reading Room Knowledge Base is considered to be the highest quality, deepest collection, of information on Alzheimer’s and dementia in the world.
https://bit.ly/2LwvkTc

#light #brightlight #nursinghome #assistedliving #adultdaycare #activitydirector 

#education #society #alzheimersreadingroom



#GlobalSurvey

PLEASE CAN YOU PARTICIPATE & SHARE, THANK YOU  🙂

  #  

 #Rheumatic # Musculoskeletal #RMD #SoMe #SocialMedia

Shared via Simon Stones | Twitter | 28 May 2018

Do you have a rheumatic and musculoskeletal disease ()? If so, you’re invited to take part in a global survey looking at what people with RMDs think about using for health-related purposes.

To take part follow this link to the study >>>

www.soscisurvey.de/socialmediarmds/

About Simon >>>

Follow on Twitter >>>  Simon Stones  @SimonRStones

BSc (Hons) • Doctoral Researcher in Child & Family Health •  &  Member •  &  Trustee • Patient Consultant/Leader

 



#whitepaper

 #PopulationHealthManagement #NHS #IBM #GGI 

WHITEPAPER | Thought Leadership Mailer – How Population Health Management will deliver a sustainable NHS ( GGI & IBM Watson Health ) | Digital Health e-news | 29 June 2018

IBM sign-up required to read

Link to Digital Health e-news >>>

Sign up for newsletters and for more Digital Health news via this link  >>>


White paper details  >>>

Title: How population health management will deliver a sustainable NHS
Date: February 2018
Authors: Andrew Corbett-Nolan, Chief Executive, GGI Divia Mattoo, Consultant, GGI Laura Tantum, Project Manager: Knowledge and Research, GGI 

Reviewed by: Darren Grayson, Director of Delivery, GGI
Designed by: Emiliano Rattin, Creative Manager, GGI


Digital Health Intelligence
Digital Health features are managed and maintained by Digital Health Intelligence © 2018
Registered Office: China Works, London SE1 7SJ Registered No. 9257440 | Vat No. 198 353 171

 



Sorry for any inconvenience as we go through a bit of website restructuring

My Disability Matters News & Opinion Digest has moved to it’s own space and all attempts will be made to update daily.

Paper.Li newsletters have also moved to their own digested post and they update themselves. 

Many thanks



 

LATEST ISSUE!

FLARE MAGAZINE  #fibro  #ME  #CFS 

Flare Magazine | The ultimate guide to Fibromyalgia, M.E & Chronic Fatigue 

July 2018

Read the magazine via this link >>> 

Flare – The ultimate guide to Fibromyalgia, M.E & Chronic Fatigue

Why not visit Flare magazine website and sign up for the magazine >>>

Flare Magazine website 



#ThePsychologist  #Research  #magazine  #BPSResearchDigest

BPS Research Digest  | 28 June 2018

‘Every week we bring you engaging reports on the latest psychology research. Anyone can subscribe free. We also provide daily updates on the latest psychology research via our app and on varying social media channels.’

The Psychologist is the monthly magazine of the British Psychological Society that you can find via this link  >>>

Visit The BPS website and opt-in for news updates and newsletters  >>>

Find BPS Research Digest on Twitter >>>


The British Psychological Society is a charity registered in England and Wales (SC039452), and Scotland (229642).
Copyright © 2018 The British Psychological Society, All rights reserved.

 



#MS  #multiplesclerosis 

The Buzz, MS Society | Sit back and catch up on the latest MS news and stories | 29 June 2018

Featuring  >>>

  • Watch: Treatment Stories

Treatment Stories, includes honest accounts from people with relapsing MS about their treatment decisions.

  • Dealing with Dr Google
  • The impact of the PIP 20 metre rule
  • Risk factors for early progression
  • Play our Summer raffle!

Read these via the following link  >>>

You can find out more about the MS Society and subscribe for the’The Buzz’ Newsletter  >>>


MS Society

Privacy & Cookie Notice

Registered charity nos 1139257 / SC041990. Registered as a limited company in England and Wales 07451571

 



 

 

#MEAction Daily Digest | Main Headline:  Volunteer of the Month: a Scottish Trio | 30 June 2018

Introductory lines:

This mother has testified before the Chronic Fatigue Syndrome Advisory Committee (CFSAC) more than 20 times about the need for urgent action from the Health and Human Services. Her two sons have suffered from severe Myalgic Encephalomyelitis for more than a decade. The photo was taken of her sons one month and one day before ME devastated their lives.

Read more via the following link >>>

Catch up on the latest actions and news:

  • #MEAction Board Member, Pam Laird, Celebrates Fundraising Success
  • NIH Director: Our Judge and Jury, Prison Guard and Executioner
  • Mother Shares Heartbreaking Testimony about Sons with Severe ME
  • U.S. – Center for Solutions for ME/CFS Seeks Applicants for Community Advisory Committee
  • Australia: Mason Foundation Explores Funding ME and CFS Biobank

Visit the #MEAction website for more information and opt-in for a newsletter >>>


#MEAction Daily Digest ~ U.S. – Center for Solutions for ME/CFS Seeks Applicants for Community Advisory Committee | 23 June 2018

Visit the #MEAction website for more information and opt-in for a newsletter >>>

Do want to help with your #patientvoice and #advocate for #MEAction? this link will help show you how you can >>>

 



 

#ArthritisAwareness  #arthritis

Arthritis Action eNews |  June 2018

Opening to newsletter:

‘We are delighted to have been featured in the Sunday Telegraph’s special inset ‘Arthritis and You’ on 17th June, to coincide with National Rheumatoid Arthritis Week 18-24 June 2018.’

Arthritis Action eNews – June 2018

Visit the Arthritis Action website for more information, advice and sign-up for their newsletter  >>>

www.arthritisaction.org.uk/

 



 

#WorldHealth #healthnews #diseaseclassification #ICD11

WHO study shows drug could save thousands of women’s lives

WHO study shows drug could save thousands of women’s lives

Including  >>>>

In case you missed it… 
ICD-11: Classifying disease to map how we live and die > explore it in more detail via the link on the newsletter.

www.who.int

 



 

unknown source

Stanford Looking At TMS to Treat CRPS  |  Ed Coghlan | National Pain Report | 23 June 2018

Opening paragraph:

Stanford University’s Systems Neuroscience and Pain Laboratory is conducting a study to test if Transcranial Magnetic Stimulation (TMS) can reduce pain related to Complex Regional Pain Syndrome (CRPS).

Read more via this link  >>>

More from  Ed Coghlan

Read more via the National Pain Report website and opt-in for newsletters >>>

nationalpainreport.com



Please note that I have opted-in to receive all the newsletters that I post from and also please remember to read the privacy policies, including ours which can be found at the end of this newsletter.

Also, due to the excessive amount of newsletters not all will get updated daily!

If you like what you read PLEASE remember to share and opt-in

Many thanks

 



Latest!

MSWorld, News, Events & More!  |   25 June 2018

Keeping you up-to-date on all things #MS & #MSWorld

MSWORLD EXPRESS NEWS

The Magic of Helping Others Started Here, Happens Here, and Will Continue Here!



 

UPDATED

Daily #MHAM Headlines

Daily MHAM Headlines for June 30th

 
Posted in 

©2018 Coalition For Headache And Migraine Patients. All Rights Reserved

PRIVACY POLICY



 

#Arthritis  #HealthCareCosts  #Misdiagnosis  #SunProtection

News and Updates from the Arthritis Foundation ~ MAY 2018| 25 June 2018

Headlines >>> 

Matt Iseman Gets a Grip on Arthritis

Prescription Rebates to Lower Health Care Costs

Red Flags to Help Dodge a Misdiagnosis

Summer Sun Protection Tips

Read them all via the following link >>>

Plus many more articles / posts, and more readables, from The Arthritis Foundation follow this link where you can also opt-in for newsletters >>>

www.arthritis.org


Living With Arthritis
Arthritis is painful. It prevents us from leading active, healthy lifestyles. It means we are more likely to develop other serious illnesses. It means we need to fight harder. The Arthritis Foundation is leading this fight by offering simple, yet effective ways to conquer the everyday battles and take control of your condition.



#biopharmanews #pharmanews #pharma

BioPharma Dive’s Top News  | Weekender | June​ 30,​ 2018

Top headliners:

  • Novartis to spin out Alcon into standalone device company
  • Sanofi Pasteur on dengue and the changing vaccine landscape
  • DIA18: CRISPR, AI, blockchain and the future of drug development
  • Roche aims for first-mover edge in small cell lung cancer
  • DIA18: Value-based contracts pose more questions than answers

  • SPONSORED CONTENT BY MEDIDATA
    Enhance precision oncology trial success

  • Immunotherapy advances spur new look at cancer vaccines
  • Why be a vaccine company?

OPINION POLL | BROUGHT TO YOU BY MEDIDATA

There’s been a lot of buzz around patient centricity. Every day this week, we’ll be asking a question to get to the heart of its impact on the industry.

Check the newsleter to see what today’s poll question is!

Read the above and much more via the following link  >>>

 



#health #spoonie #backpain #chronicpain #drugs #fibromyalgia #pain #medication

12 things you can do to pamper yourself|  BARMAC5  |  BACK PAIN BLOG UK…  |  26 June 2018

About ‘BackPainBlog’, Quoted from the site:

‘A PERSONAL JOURNEY OF A CHRONIC BACK PAIN SUFFERER. MY SITE IS FULL OF THE LATEST TREATMENTS, PRODUCT REVIEWS, THERAPIES, DRUGS, TIPS AND WEBSITES ON BACK PAIN, FIBROMYALGIA AND ARTHRITIC CONDITIONS.’


 

Follow the link below to read more  >>>

12 things you can do to pamper yourself

Why not visit Barmac5’s blog on WordPress for more chronic pain and fibromyalgia related posts  >>> 

BACK PAIN BLOG UK…



 

#men get migraine too #menshealth #migraine 

Living the Minority: Life as a Man with Migraine |  BY JASON (GUEST WRITER)  | The Migraine Mantras | 17 June 2018

Opening lines:

‘Males are the migraine minority. Women are 3x more likely to have migraines than men. Being a male with migraine, let me share a bit of my experience with migraines.’


Read more via this link  >>>

Visit ‘The Migraine Mantras’ website for more migraine related posts >>>



#healthcarenews  #patientengagement  #healthcare #patients 

Latest! MedCity News | Title: Meet the “preeminent AI company on earth,” but can it succeed in healthcare? | 20 June 2018

Second paragraph of About Us page of the MedCity News website:

‘Healthcare leaders must stay on top of new technologies, new companies, future trends and the latest policies, with a perspective that includes the entire healthcare ecosystem: health IT, medical devices, health systems, venture investing, mobile apps, biotech and pharma. In this interconnected market, there is no “Silicon Valley” for healthcare but nearly a dozen hubs of healthcare and life science innovation, including Philadelphia, Cleveland, Research Triangle Park, and Minnesota’s Twin Cities, Seattle and San Diego’

Follow this link to MedCity News About Us page  >>>

Read the MedCity News ~ TOP STORIES newsletter via the following link >>>

 

Follow this link to MedCity News ~ patient engagement section  >>>

Follow this link to MedCity News Home Page where you can opt-in for their newsletters  >>>

 



 

#PatientExperience  #professionals 

WHITEPAPER ~ Improving Patient Experience |   | Siemens Healthineers  |  13 June 2018  

Introductory line:

Do measures to improve patient experience increase quality of care, hospital efficiency, and patient loyalty?

Read the report by following this link  >>>


Who are the ‘Siemens Healthineers’?  >>>

Opening paragraph from About Us page:

At Siemens Healthineers, our purpose is to enable healthcare providers to increase value by empowering them on their journey towards expanding precision medicine, transforming care delivery, and improving patient experience, all enabled by digitalizing healthcare.


Visit this link to opt-in and register for newsletters  >>>

Siemens Healthcare GmbH ©2018

 



#Rheumatology resources for #professionals and #patients

 

EULAR websites >>>

EULAR Congress website: www.congress.eular.org

EULAR Congress 2018 documents: www.congress.eular.org/download.cfm

EULAR website: www.eular.org

EMEUNET website: emeunet.eular.org

EULAR Young PARE website: www.youngpare.org


Welcome message from Johannes W. J. Bijlsma for the ‘Annual European Congress of Rheumatology’ who is EULAR President  >>>

Welcome message from the EULAR President


Did you not get to Amsterdam for the ‘Annual European Congress of Rheumatology‘?

Well don’t worry too much there are a few ways that you can keep up to date with what went on.


 

The (EMJ) European Medical Journal will have a full congress review of in their next edition of EMJ which is FREE to subscribe to via this link >>>

In the Meantime…

… you can see all of EMJ’s Rheum content by visiting this link, please share. Please opt-in & help me to get proper peer reviewed articles out there  >>>


PLEASE NOTE:

Copyright © 2018 European Medical Group LTD trading as European Medical Journal. All rights reserved. European Medical Journal is for informational purposes and should not be considered medical advice, diagnosis or treatment recommendations.


 

#healthcareprofessionals #MedicineMatters

Medicine Matters | medwireNews@EULAR2018

Medicine Matters is developed for healthcare professionals as a premier resource for the latest clinical information in medicine.

FREE registration for Medicine Matters ~ Rheumatology, you can opt-in via this link >>>

Rheumatology Matters twitter feed >>> 

 



Sorry for any inconvenience as we go through a bit of website restructuring

My Disability Matters News & Opinion Digest has moved to it’s own space and all attempts will be made to update daily.

Paper.li newsletters have also moved to their own digested post and they update themselves. 

Many thanks

 



#LymeAwarenessUK

Improve NHS testing for Lyme Disease, fund research & revise current treatment protocols

Can you help to bring better awareness of #lymedisease to the UK & sign this #Petition to improve #NHStesting, #research & recieve better funding to help this cause.

NHS Choices say ‘Lyme disease is a bacterial infection that can be spread to humans by infected ticks. It’s usually easier to treat if it’s diagnosed early.’

Read more via the petition link below the butterflies

#LymeAction  #Lymetoo 
Many thanks for reading & helping to raise awareness

🦋💜🦋

Improve NHS testing for Lyme Disease, fund research & revise current treatment protocols.

Petition Via >>>  www.change.org

 



#arthritis #rheumatologists #rheumatology #fellowships #ACR

Arthritis Foundation ~ Champion Connection |June 2018  Newsletter  | 15 June 2018

Opening paragraph:

‘The Arthritis Foundation is actively expanding the number of rheumatologists by naming five universities that will receive fellowship awards. The program is designed to address the growing shortage that the American College of Rheumatology cautions is expected to increase and will lead to worsened disease outcomes, lower quality of life and increased mortality rates.’

Read more via the following link  >>>

Plus many more articles / posts…

For more readables from The Arthritis Foundation follow this link  >>>


Living With Arthritis
Arthritis is painful. It prevents us from leading active, healthy lifestyles. It means we are more likely to develop other serious illnesses. It means we need to fight harder. The Arthritis Foundation is leading this fight by offering simple, yet effective ways to conquer the everyday battles and take control of your condition.

 



 

#health #spoonie #backpain #chronicpain #drugs #fibromyalgia #pain #medication

The effect on family support on patients who are suffering from fibromyalgia or chronic pain |  BARMAC5  |  BACK PAIN BLOG UK…  |  30 June 2018

About ‘BackPainBlog’, Quoted from the site:

‘A PERSONAL JOURNEY OF A CHRONIC BACK PAIN SUFFERER. MY SITE IS FULL OF THE LATEST TREATMENTS, PRODUCT REVIEWS, THERAPIES, DRUGS, TIPS AND WEBSITES ON BACK PAIN, FIBROMYALGIA AND ARTHRITIC CONDITIONS.’


Opening paragraph:

‘The effect on family support on patients who are suffering from fibromyalgia or chronic pain is an essential factor in the care of these conditions. While only one person in a family may suffer from fibromyalgia or chronic pain. the entire family is affected by it.’

Follow the link below to read more  >>>

Why not visit Barmac5’s blog on WordPress for more chronic pain and fibromyalgia related posts  >>> 

 



#careactionplan #carersweek2018 #carers #policypaper

Policy paper | Carers action plan 2018 to 2020 |  Published 5 June 2018

The plan sets out how the government will improve support for carers in England over the next 2 years.

www.gov.uk/government/publications/carers-action-plan-2018-to-2020

For all kinds of useful Gov type information and useful links visit their home page  >>>

www.gov.uk/

 



#EMR  #HIPAA  #Healthcare #Technologies #digitaldevices #digitaltechnology

Creating Provider Loyalty – And Why Communication Matters |  John Lynn | EMR and HIPAA Newsletter | 15 June 2018

Featured Health IT Resource

FREE DOWNLOAD  Top 5 Medical Device Industry Trends in 2018

Digital device technology continues to move at a fast pace, which means device manufacturers should keep a close watch on emerging trends and be ready to adapt to new ideas and methodologies.

Read Creating Provider Loyalty – And Why Communication Matters via the following link  >>>

The following is a guest blog post by Chelsea Kimbrough from Stericycle Communication Solutions, as part of the Communication Solutions Series of blog posts. Follow and engage with them on Twitter: @StericycleComms

For more articles / posts visit the website where you can also opt-in for newsletters  >>>



 

It’s that time of year to recognise your peers, your fellow advocates and patients leaders.

WEGOHealth Awards

Nominations have officially opened. Head on over to the WEGO Health Awards nomination page to recognize your favorite community leaders.

Everyone can be a part of the #WEGOHealthAwards!

Make sure to nominate your favorite Patient Leaders across all condition areas and topics, including

#chronicillness #invisibileillness #fibro #ME #EDS #Lupus #Musculoskeletal #RMD #arthritis #psoriasis #chronicpain #multumorbidities #patients #patientvoice #collaberative #TEAM #PatientLed #PatientEngagement

#patientadvocacy #healthadvocacy #researchadvocacy

#ChronicillnessVOICE  #NotJustPatients

 



#science #cancer #cancerresearch #immunotherapy

#lungcancer #vaping #breastcancer

News digest -scienceblog~Cancer Research UK  |  lung and breast cancer immunotherapy and vaping |  Katie Roberts  |  9 June 2018

Breast cancer immunotherapy first ~ opening lines

A woman’s advanced breast cancer has apparently been eradicated by an experimental therapy made from her own immune cells, reports the Mail Online. The woman remained cancer-free two years after the “highly personalised” therapy, after existing treatments had failed.


You can visit the scienceblog~Cancer Research UK via this link >>> 



Change-over NEW PODCAST

Airing Pain Programme 103: Pain and Relationships |  Pain Concern  | 6 June 2018

Airing Pain ~ Informing the pain community
Programme 103: Pain and Relationships
How pain’s unpredictability can affect interpersonal relationships, and recognising help when it appears.

In this edition of Airing Pain, Paul Evans and eminent psychotherapist Dr Barry Mason speak about their personal experiences with fibromyalgia and ankylosing spondylitis.

 

How pain’s unpredictability can affect interpersonal relationships, and recognising help when it appears.

This edition of Airing Pain is funded by the JTH Charitable Trust and the Persula Foundation.

Airing Pain channel on Audioboom >>>

Pain Concern website >>>

 Copyright © 2017 Pain Concern, All rights reserved.

 



#Fibromyalgia  #Research #FibroResearch

Fibromyalgia Research Newsletter  | UK Fibromyalgia |  June 2018

Fibromyalgia Research Newsletter June 2018


The home of the Fibromyalgia Magazine- The independent voice of UK Fibromyalgia.

This newsletter is for informational purposes only and should not be used as a substitute for the medical advice or services of your health care providers.
The advertising of a product, therapy or clinic in this email does not imply that it has been tested or its use endorsed by UK Fibromyalgia.




Open Medicine Foundation®
Fast-tracking revolutionary research for ME/CFS
and related chronic complex diseases
OMF is a non-profit 501(c)(3) organization
(EIN# 26-4712664). All donations are tax-deductible to the full extent allowed by law.

Visit the OMF website for news and other interesting readables, you can also opt-in for newsletter updates >>>

Open Medicine Foundation

 



#stemcells #Lyme  #LymeDisease ##healing #healthjourney

Ten Months Post Stem Cells – A Snapshot Into My Lyme Disease Healing Journey |  Terry Mayfield, The Blathering Lymie |  Color Me Lyme  | 31 May 2018

Excerpt:

‘I am, however, tickled pink to share I’ve experienced noticeable improvements recently. Crazy thankful for forward progress, albeit slow. A smidgen of reluctance comes over me as I type the words “noticeable improvements” and “forward progress”. I don’t want to mess with this positive juju!’

Read more via this link  >>>

About the Author  >>>

For more blog posts and newsletter opt-in visit the site  >>>



#NHS70 #NIHR  #IAmResearch

Please sign and support new research

Thunderclap ~ NIHR I Am Research & NHS70 |  by The National Institute for Health Research (NIHR) |

Thunderclap ~ NIHR I Am Research & NHS70

I share this campaign as a Patient Research Ambassador for NIHR #PRAI

Carole Sian Scrafton ~ CEO FibroFlutters / Founding Five Member FibroFlutters / Patient Group Leader / Patient / Patient Expert

#ResearchAdvocacy #HealthAdvocacy #PatientAdvocacy

 



Excellent newsletter!

Girls With Guts  (GWG)| May 2018 Newsletter | Get in the spirit! |  2 May 2018

Visit the site to find out more about GWG and the work they do >>> 

 



#backpain #chronicpain #muscles #rhomboidmuscles

Debilitating Diseases newsletter | Subject: Everything You Need To Know About Your Rhomboid Muscles And Upper Back Pain | 9 May 2018

Home Page >>>

 



#RareRevolution #raredisease #rarebabies 

Spring has sprung and our RARE Babies issue is here! | Rare Revolution Magazine | Spring 2018

Quoted from e-news mail:

‘This issue is themed around the joy that RARE BABIES bring to our lives and the challenges we face raising and battling for them, along with the bitter sweet moments of a battle lost.’

Visit the magazine website via this link and sign up for the quarterly FREE digital magazine and also read back issues >>>



Newsletters from News-medical | Life Sciences >>>


News Medical | Arthritis Newsletter | 3 April 2018


News Medical |Allergies Newsletter | 15 May 2018 


News Medical |Dermatology Newsletter | 31 May 2018


LATEST!  Newsletters from News Medical |Genetics | 27 June 2018  


LATEST!  News Medical |Neurology / Neuroscience Newsletter | 20 June 2018


LATEST!  News Medical |Pharmacy / Pharmacology Newsletter | Headliner:  People who use medical marijuana have higher rates of prescription drug use, study finds |  22 June 2018

 


New!  News Medical |Psychiatry Newsletter |  7 June 2018  

 


 

Latest!  News Medical  |  Rare Diseases  |  23 May 2018 

 


Latest!  |  News Medical |Rheumatology Newsletter |  Headliner:  Simple changes to diet could help reduce osteoarthritis symptoms|  1 June 2018  

 





Meditation Change over!   

KUNDALINI RISING || 432Hz Music to Balance Male Female Energy || Healing Music for Meditation | June 2018

Meditative Mind  Published on 7 Jun 2018

If you enjoy this then please visit >>>

Via:  www.youtube.com



 

Every morning and evening I was posting several links to a variety of online newspapers and thought that maybe I could post twice a day from here, our website/blog, Morning and Evening Post instead.

This is to ensure that all the news and stories go out to everyone that follows us across the social media platforms that we have profiles/accounts.

Here’s a few links to my favourite online newspapers for finding a variety of health related news from other Chronic Illness Bloggers & Warriors, for up to date news about health conditions such as latest research papers or people sharing hints and tips about how they cope day-to-day.

Also like to share other posts by fellow bloggers and organisations too

Let us help them by showing our support by sharing the news and stories that they share.

If you publish a health related paper.li or other health news magazine/paper that isn’t listed and you would like it to be, please contact me – Carole Sian at fibroflutters@gmail.com and let me know, always happy to help 🙂


Many thanks for reading and helping to share the news that other folks like you write, or, find.

😀


 


PLEASE NOTE:
  • That here at fibroflutters.com we are not medical professionals just fellow chronic illness warriors sharing information.
  • Any information read or shared on, to or from this blog site should not override any advice given to you by your own Doctors.
  • FibroFlutters is not a selling site but we will point you in the direction to subscribe to newsletters/magazines and some offer free, some don’t! 
  • The opinions expressed on this blog represent the author’s own views and not necessarily those of FibroFlutters, fibrofly73 or any other author on this website. We encourage you to share your own views in the comments section.
  • Our sharing of these articles and posts does not necessarily mean endorsement of them, and we recommend that you check for validated sources and peer reviews.  It also does not mean that we are affiliated with anyone unless it is clearly stated.
PLEASE:
  • Do not take any work, articles or pages to be your own, including those from third partie, or any external partie links, and always accredit the appropriate authors accordingly.
  • Always speak to your GP first before stopping, changing or trying new medications or treatments, FibroFlutters will not claim responsibility for any loss or damage from third parties/third partie links, or any external parties..
  • Always be aware of Internet security and note that we cannot be held responsible for external websites.
  • Remember that buying products such as ‘cure-claiming’ remedies on-line can be a risky business and again FibroFlutters will not claim responsiblity for any loss or damage from third parties/third partie links or any external parties.

Please can you read our ‘Disclaimer’ & ‘Privacy’ notes and if you have a problem we are always open to discussion, just e-mail Carole fibroflutters@gmail.com

🙂
FibroFlutters ~ CHRONIC, INVISIBLE AND RARE ILLNESS SUPPORT / ADVICE / ADVOCACY| Disclaimer | Privacy Notes | 8 May 2018