People with Multiple Sclerosis face ‘disturbing’ levels of workplace mistreatment says recent research! Was this true for you? Take our poll! Updated

Types of multiple sclerosis

Types of multiple sclerosis

According to the UK’s MS Society “24% of people with MS say their employer has treated them badly as a result of their condition, and a fifth say their colleagues have.” This is according to their latest survey findings, which investigated discrimination at work for PwMS.

And “Of the people who say they have faced mistreatment from their employer, 91% say their employers knew they had Multiple Sclerosis. And 85% who faced mistreatment from their work colleagues say their colleagues were aware of their MS.

In the survey, people shared many distressing experiences of mistreatment. These included facing offensive and humiliating comments, feeling bullied and being accused of looking too well to have an illness or disability.

People also say they have lost out on promotions, been forced out of work unfairly and had requests for reasonable working adjustments denied.”

Michelle Mitchell, the Chief Executive of the MS Society shared “Our survey clearly shows the need for a shift in attitudes to better support people with long-term conditions and disabilities to stay in work. It’s disturbing to hear so many accounts of people being bullied and mistreated at work because of their condition, especially as people with MS are protected against discrimination under equality law.

“We know that some people with MS absolutely won’t be able to work because of their condition, but for those who can, simple adjustments and supportive employers can make a huge difference. We want to see more positive workplace cultures that value the important contributions that people with MS can make.”

So what about you?

Have you suffered from discrimination in the workplace because of your multiple sclerosis? Why not take our poll below.

 

TimDyer I was a Union electrician. After my DX I got a phone call from our local President. He said “well, you can’t be on boom lifts or 20 ft ladders, and we can’t sell you as a full fledged union electrician anymore. You should go on Disability”. He gets a pass because I got worse, but he’s still an asshole in my book.

The Ultimate Guide to Multiple Sclerosis Valuable new resource from GeneFo for the Multiple Sclerosis Community

Guide to Multiple Sclerosis

Guide to Multiple Sclerosis

A valuable new resource from GeneFo for the Multiple Sclerosis Community.

GeneFo has recently created a useful free resource for the MS community. A guide that offers expert advice on nutrition and exercise best practices, tips for the newly diagnosed, innovative treatments you need to know about, daily hacks, parenting issues, clinical guidelines, and social/emotional recommendations. You can get a sneak peek by clicking here, where you can also sign up to get your free copy!

Multiple sclerosis – What one piece of advice would you give to somebody who has just been diagnosed with multiple sclerosis?

What one piece of advice would you give to somebody who has just been diagnosed with multiple sclerosis?

What one piece of advice would you give to somebody who has just been diagnosed with multiple sclerosis?

Many years ago when I worked in the field of medical market research I was given one very useful suggestion when conducting interviews with people with different medical conditions. My, then, Colleague said I should always ask a respondent what piece of advice should they give to a person who has just been diagnosed with a particular medical condition.

Remembering this recently I thought it might be useful to ask our readers on the MultipleSclerosisTalk page on Facebook the simple but vital question “What one piece of advice would you give to somebody who has just been diagnosed with multiple sclerosis?”

I have to say the results were fascinating. So I decided to share a few here. If you have any ideas or tips of your own please do write then down in the comments box below.

First off Sophia was please we asked the question. She mentioned “I just found out and I am still absorbing it all while having doctors who will not take the time to explain the implications… I’m happy for this group because I am learning what the doctors won’t tell me.”

One of the most popular suggestions came from Christa. She advised “Learn quickly that your life will change… But don’t obsess over the diagnosis… Adapt… Be strong… Don’t sink into it and wallow in it ….or it will quickly overtake you emotionally… Just my opinion ❤️
Having said that…. Do educate yourself… Be a smart patient… And don’t let them drug you to death… Take what you have to but note some docs will put you on a new pill for every single little thing and you’ll quickly become a mini pharmacy…” In fact a lot of what she has to say applied to pretty much any medical condition and it is great advice.

Looking at it from a more personal situation Linda “Allow yourself time to grieve. That’s the best advice I have received. I would allow myself 15 minutes (to cry in the shower) and then carry on with the day. Also, whenever you have flair, I tell myself “this too shall pass”. Be kind to yourself. Hugs and prayers to you”.

“It is NOT THE END OF THE WORLD. I thought so when I got diagnosed. I was depressed in the hospital that evening and the following weeks. But after fighting it by eating healthy and exercise, my MS has been inactive (remission) for a little over a year now. Listen to your body. If you are tired, rest. Don’t try to push through it.” Shared Jaime!

Suzi and Katie focus on their relationships with others. “It sucks and your life will change. Accept support from your family and friends and try not to get mad when they’re being over supportive. You’re not the only one affected. Don’t read the horror stories of how you’ll be in a wheelchair and die young. Most of all think of the disabled parking sticker you get and how much easier Christmas shopping is 😂” said Katie.

While Suzi shared “Don’t let people push you around. If you’re too tired, didn’t remember, or are too weak to do something and someone puts you down because of it and says you’re just making excuses you need to cut them out of your life because all that does is stress you out and bring you down. At the end of the day a good support system is all you need.”

Finally Fiona spoke for many of our readers “Listen to your body. Read and make your own decisions as to what you believe your MS is. No two are the same and only you will know how your MS affects you and the triggers for you.”

As I we said earlier if you have any tips you would like to share please feel free to use the comments section below!

Many thanks in advance!

 

ANGIEDEE I have just been diagnosed with MS, well about 2 months ago. And even though all this is still new to me I would say this; find yourself a doctor who listens to you, and cares about your wants. One who does not just want to shove pills down your throat but offers you good, natural and healthy alternatives. One who encircles you to take up yoga and find way to manage stress levels. And above all else, keep a positive attitude! What I have come to realise, is that this is not a death sentence, it is a life sentence, so make the most of it, become healthy, and keep moving forward.
hahamed1964 Just cut out the junk food and preservative materials and drink just natural juices ,I garantee you’ll stop the progression 100% . I don’t take any medicines nor injections since 2002 .

Deliver the dream – a retreat for families with a parent with multiple sclerosis

Win a family weekend retreat. Deliver the Dream provides a weekend retreat complete with food, entertainment and lodging to Florida families affected by MS. Children must have a parent with MS or have MS in order to apply. Application deadline is October 11. If accepted the retreat is November 11-13 in Haines City near the Orlando area.

https://www.surveymonkey.com/r/2016DTDRetreatApplication

 

Retreat for families with a parent with multiple sclerosis

Retreat for families with a parent with multiple sclerosis deliver the dream

 

Invitation to a free webinar “A Review of Natural Treatments for MS Symtoms” with Dr. Trent Austin. Hosted by GeneFo September 8th, 2016 1PM EST/ 18:00 UK

Natural treatments for multiple sclerosis

Natural treatments for multiple sclerosis

A very exciting and informative webinar coming your way J
Join Dr.Trent Austin for a live online lecture (or get the video recording) on natural treatments for MS symptoms- including Biotin, Vitamin D, Turmeric (curcumin) and more…

Dr. Austin has been incorporating natural therapies into his practice and researching the effects of these remedies on symptoms of MS. He will summarize clinical studies in easy-to-understand terms; offer opinions based on his research, and speak about safety, recommended dosages and reliable sources.

Register today at www.genefo.com/webinarms (if you cannot make the session, please feel free to register and you will automatically receive the recording)

Registering for the webinar unlocks many other great features for MS patients and caregivers, delivered on GeneFo:

GeneFo is a free patient crowd sourcing platform that innovates by going beyond matching patients that have the same condition, and actually classifies & matches them according to their specific Multiple Sclerosis type.

Patients and caregivers can use GeneFo to

  • Track their condition via personal health management reports
  • View and compare real-time stats on what works for others with a similar medical profile
  • Register to get matched to clinical trials according to location and profile
  • Consult with an in-house medical team
  • See unbiased reviews of medical & alternative treatments and providers

 

And the best part?  No more sifting through endless posts and web pages – All of these features are perfectly organized and delivered in one screen!