Modern Friendships 

In a world as connected as ours, friendship spanning across the globe is a simple evolution. This morning I saw that Facebook has surpassed 2 Billion users each month. Taking into account other Social Media platforms such as, Twitter, Instagram and Snapchat it is no wonder our modern society has developed into what we take for granted today. 

Friendships are formed out of mutual interests, mutual goals & aspirations and an overall sense of “community” with another person. It used to be that friends would meet up and go out to a restaurant, coffee shop or simply to one another’s home. Not to say this has stopped occurring, rather society has greater means to meet up. There are groups within Instagram called PODS, Twitter groups that will engage in conversation through the use of hashtags and of course Facebook groups or forums. 

Years ago, I was introduced to an amazing group of individuals through Twitter under the hashtag #ChatMS. This group continues to engage in MS related topics each Monday at 7pm EST. After my first experience with #ChatMS, I quickly saw the value in what the goal of the conversation was. I connected with a wide array of people from across the world whom face same or similar issues with the disease that I do. This experience was life changing for me. I found a venue where I could openly discuss my experiences with the disease while also hearing of others’ battles as well. A concern for some, is that when using Twitter just about anyone can read what you post by searching the hashtag #ChatMS. 

To resolve this, the creators behind the Twitter initiative, who previously formed a Facebook private group under the name ‘Must Stop MS!-Keep S’myelin’, created a new Facebook closed group also called, #ChatMS. In this way, the topics and questions could now  be engaged on Twitter alongside a closed Facebook group, allowing for greater privacy. A quick search of MS groups online will give a multitude of results. Personally, I have found #ChatMS to be one of my personal favourites. This is not to mean the other groups out there are not supportive, rather I have and continue to build strong friendships from this group. In actuality, #ChatMS has introduced me to various other MS groups which I find great value in! Just as members of these other groups were introduced to the Twitter and Facebook weekly #ChatMS conversations as well. 

For myself, Multiple Sclerosis is but just one part of my medical history. Most will know I have experienced seizures in the past related to an MS treatment I was on for some time. I’ve also had the unique experience of Pyoderma Gangrenosum, which I will be speaking to with greater accuracy in the future. Given the rarity of this disease I could not find a similar group to engage with in regards to Pyoderma Gangrenosum. To this day I have yet to find one either. I did put thought into creating my own. Although once looking at the few groups already created, there was little to no discussion over the course of years. I knew from the onset this was an incredibly rare condition, so rare in fact there simply is not a high enough base to engage in continuous conversation. 

During my research, I happened across a new (at the time) Facebook group called ‘Medical Musings with Friends’. Once reading what the group was intended for, I joined. Just as with #ChatMS, I was immediately pulled in. Pulled in to insightful conversation with those that could relate to my experiences. I have become incredibly close friends with many via this group. Even though the majority of members, at least when writing this, are in Australia. Even with a 16 and 17 hour time difference, new friendships were formed. I was eventually asked by the groups creator if I would like to be a member of the Administration Team, helping to monitor posts, engage with new and existing members as well as be able to add new members  requesting to join the group. I was taken back when given this invitation. It may not sound to excitable to some, for me it continues to be an honour. 

I have come across countless people that live with a multitude of medical issues. Some live with the same conditions as I do. Multiple Sclerosis, a permanent Ileostomy due to Ulcerative Colitis, Anxiety, Depression etc.  Although not one that has had Pyoderma Gangrenosum. Which I suppose is a good thing!

I wanted to speak to this “Modern Friendships” topic to allow others to realize they are not alone in whatever situations they may be experiencing. As more people begin to follow my modest blog, I hope this message is well received. If it were not for Randy Patrick, behind ‘#ChatMS’ and ‘Must Stop MS’ along with Sam Moss, the creator of ‘Medical Musings with Friends’ I would not have made the life long connections I have. These folks and I do share common health related conditions, more so than that we share common interests. Ranging from sports, travel, family life or just back and fourth random conversation as one would have in a traditional Coffee Shop. 

For those reading this who may feel lost or alone, take comfort in knowing there is a world of support literally at your fingertips. Likeminded individuals who simply will read what you need to say, and offer advice or a simple modern ear to just listen. 

Below are the groups I spoke of, unfortunately I was unable to imbed direct links via WordPress. If you have difficulty finding these groups and wish to join, do not hesitate to send me a message. 

#ChatMS on Twitter and Facebook

Facebook Closed Group

Facebook Closed Group

12 thoughts on “Modern Friendships 

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  1. Great post Dave! Agree that the wonderful networks of like minded people spanning the globe are a bonus of our modern social media age. Friends are friends. No matter where or how they are connected. X Esther

    Liked by 2 people

  2. Great post xx I love that we can all connect all around the world. Times have certainly changed. I can now sit at home or in a cafe anywhere in the world and chat to my wonderful friends via Social Media. Its like they are sitting in the cafe with me. I do not feel alone anymore.

    Liked by 2 people

  3. I couldn’t agree more Dave. Great post. Some of my closest friendships are with those of you who journey with me online across the seas. Social Media used for “good” purposes is a real gift to our modern age, especially for those of us living with chronic disease.
    Thanks Dave for highlighting the part Medical Musings with Friends plays in creating these special connections.
    I’m so glad you found the forum & not only are you a wonderful admin but I also found a great friend.
    Sam xx

    Liked by 1 person

  4. Medical Musings with Friends ? How fabulous! I am not in this group, but Sam Moss who ran the SwellGals arthritis group I am in is ( as you know) the Creator of MMWF.
    I’m so glad you’ve found a place to chat with other peeps who have the generous and varied aliments / illnesses etc that Sam and yourself have.
    I’ve only got a couple, so am not part of that page. I was in a very dark place when I came across Swell Gals, and, it was the uplifting posts from Sam, no longer feeling alone , and how she continues on with such a great attitude that helped me get away from the dark hopelessness and doing a little more every day.

    I’m so glad you found that group!

    Liked by 1 person

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Living my best frugal life, smashing debt and chasing F.I.R.E with an ostomy!

Joint Purpose

Living With Joint Pain

Invisibly Me

Live A Visible Life Whatever Your Health

A Chronic Spoonful

Thoughts and stories from the world of chronic pain, illness, and disability

Poorly parents, mummy with MS

Being a parent and managing a chronic illness

Bethy Bright and Dark

My MSAdventure

Diabetes Blog - Happy-Medium.net

Searching for the right balance between the highs and lows of diabetes

my oms life

mum, psychologist, researcher & overcoming MS with a new way of living through Overcoming Multiple Sclerosis lifestyle approach (OMS)

Beautifully Raw

Cultivating Wholehearted Living

PainPalsBlog

My family and friends living with me.....and chronic illness

The Anxious Optimist

Know your worth.

OCD meets MS

The ultimate battle. . .

RibbonRx

Raising Awareness About Life

Fightmsdaily

Living life with a chronic illness is definitely not easy. But I do my best to push through all the barriers this illness puts in front of me! In my heart and mind, I believe maintaining a positive outlook on all situations in life will carry us through to much better times! I hope you find the information that I provide both helpful and inspirational!

swanyriver

Swimming as hard as I can to stay afloat!

FibroFlutters Patient Advocacy Organisation | Chronic Illness & Rare Disease Network

Patient, Health, Research, Medical, Clinical, Digital Health and Pharma news, information, communications, advice, reviews and resources

InsideOutlet

Living my best frugal life, smashing debt and chasing F.I.R.E with an ostomy!