MDJunction - People Helping People
 

MDJunction to me

nona7"MDJ is a place I can get advice, share my fears and concerns, Share my personal story, and make friends with people who truly understand where I'm coming from.
When I was first diagnosed with CHF I was so scared the people in the Chf support group helped me through a very bad time.
I am now also a member of PAH and MVP groups.
Thanks to MDJ I can talk to people who truly understand!
" (nona7)

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RLFORTIN
RLFORTIN
Rank Member
Online Status OFFLINE
Member Since 04/18/2012 05:58 PM
Last Online 05/20/2012 04:06 PM
Gender: Female
City: Oceanside
State: California
Occupation: Pround SAHM & USMC wife
A little about me: I am a 36 y/o Proud Marine Corps Wife and Proud SAHMommy of two beautiful, young daughters. I also have an identical twin sister with ALL of the same health issues as I.
I was dx'd with Fibro in 2009, but beleive that I have been suffering with it for MANY more years.

Along with Fibro, I also have Endometriois, SI Joint syndrome, Hemiplegic Migraines, Neuropathy, Morton's Nueromas.

Meds: Cymbalta, Norco, Propranlol ER, Soma, Cetirizine, Vit D3, Omega3-6-9, Q10.

~~You will not find peace, until you find all of the pieces~~
My Awareness Ribbons
 
"I wear the purple ribbon for Fibromyalgia awareness and support."
 
"I wear a yellow for my Husband who has survived testicular cancer."
 
"I wear a pink ribbon for my Aunt, who has battled Breast Cancer."
 
"I wear this ribbon for my lovely newphew with Autisum : )"
 
"I wear the silver ribbon to help raise awareness for those living with Parkinson's. My G-ma lived with it for years before passing away. RIP G-ma : )"
Awareness Ribbons

My Hugs
Clarita gave me a Hug
04/10/2014 03:38 PM
a HugHello :-), Group Hug time from your Group Leader Clarita,
Please check out all the new posts over on Chronic Pain Support Group plus if you are able to join in then please freely do so plus thanks in advance for this- this would be fabulous(only if you can post as your pains are not too high or you are not too busy or both of these) if able to join in then do so - refuse to sit on the sidelines- be active/proactive as the more that join in the better it is for the dynamics of the group :-) so the better it is for us all!

Very warm welcome to all new members here- make your fine selves at home with us :-)!

Respect is vital- hence my rant of a post earlier- always treat your fellow chronic pain community member with the upmost respect as well as show them gratitude whenever they take their time to help You. Manners cost little yet make a big difference. Always be civil, adult like as well as treat each other as equals, too.

Bullies will be given zero tolerance by us GL's, too.

Though, on the whole this is a supportive fabulous community even though it has been a little quiet in its voices recently(soon to change hopefully)!
It is a real honour to serve as a GL here alongside Mike and Fibroforever.

Huge heartfelt thanks for all the supportive kind messages receive regularly via private messages from you lovely people here as well as the wonderful hugs- touches me deeply to know that you care plus appreciate what do for You. So huge heartfelt thanks.

All those here holding on tightly keep holding on tightly plus know that it will pass/ease up! Lean on us here for support , too.
If you are in a good phase or just want to show you care then please reach out to your fellow chronic pain member with some words of encouragement or support.

Take excellent care of You- each one of You here, plus take brilliant care of one another. Be kind as we are all each fighting hard battles- as the saying goes!

Choose to be the best you can be plus learn to be your own best friend- make it so!

Look forward to seeing new posts as well as new faces on the support group- all who can make it happen.

Sending you my warmest wishes plus super soothing hugs, namaste Clarita :-)
namaste= the light in me honours the light in you

Clarita gave me a Hug
03/27/2014 03:27 AM
a HugHello Chronic Pain Members, Would love to see you join in with posts or create your own- do not sit on the sidelines- this group is for you all here- please make this happen! Looking forward to seeing lots of new faces as well as some familiar ones join in. If you can join in then please do so. If not able to join in then we understand, too. We all need to do what we can when we can.
Please check out the new posts here, too. There is something for everyone here on this caring group.

Please hold on tightly- everyone here whom is having a super tough time of it!
Realise you are not alone.
Take comfort in your friends.
Please lean on us here, too!
Take fabulous good care of You each (be tender/self nurturing)as well take superb care of each other here please.

Sending warmest wishes to you each plus dolphin smiles across the miles from here in the UK, love Clarita :-)
gentle hugs winging their way to you each plus wishes for good karma for every single one of you!

purpleyogamat gave me a Hug
03/13/2014 08:38 AM
a HugHello fellow Lyme Warrior :) I hope you are well. Please take a moment to check the LLMD Requests forum on the Lyme Group. We have changed how LLMD Requests are done. Please make sure any links you post have been updated to the new sticky :) blessings, purple

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