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MDJunction to me

jpcrps"When I found MD Junction, I was in the beginning stages of RSD/CRPS. I was scared, lacked knowledge about the condition, and felt very alone.

MD Junction changed all of that for me. I found friendship and terrific information from people who had first-hand knowledge of this syndrome. It was and still is a big part of my life.

MDJ was my first step on the journey of grief; from denial to acceptance. I am now inspired to help others by sharing this amazing site and sharing my own experiences. I am very impressed that one forum site can provide hope and inspiration to people suffering from so many different conditions. I am proud to be a part of this community.
~ Jenny
" (jpcrps)

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Lupus ForumsGeneral & SupportA Message to the Group
04/15/2011 06:24 AM
82nd
82nd
 
Posts: 233
Member

I have learned many things about myself from this group this week. I have learned that isolation and depression is not unique. In just a few days all of you have shown me by your example that I have lived in denial for the last four years. I’ve been living by controlling my environment and the people I work with so as to not have to be confronted with this problem or even talk about it. I have pretended that I can do the same things I did ten years ago, and even five years ago. One Monday I had no place to turn, so I signed up here. On Friday, today, you have all taught me this week that it is what it is, I don’t need to fear it, I still have something to offer others, and I am not alone. I hope everyone understands the impact you have had on me and how grateful I am that you have taken time for me, amongst your own important issues. I thank all of you from the bottom of my heart!
Ray
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04/15/2011 08:44 AM  Top
afmom
 
Posts: 736
Member

Thank you for that. But remember you always have something to share or to help or to offer someone. You are important! Don't ever forget that.

Previous discussions I participated in:
I did it!
today
please help me

04/15/2011 12:25 PM  Top
redhairali
redhairali
 
Posts: 3398
Group Leader

Isn't it wonderful to be a part of this group? The people here are so caring and are willing to share so much of their selves. Everyone is a integral part of why this group works so well. Whether you are feeling good or feeling poorly you all have something to give the group. Big hugs all around.

Alison


Previous discussions I participated in:
Really Pi@#$#@ Off
Doctors
Sunlight Exposure and Lupus

04/15/2011 05:20 PM  Top
Pandora74
Pandora74
 
Posts: 1985
Senior Member
I'm an Advocate

It is an amazing place. In my own case I came here at a time when I was just beside myself with grief and I felt so alone. I found the same thing in everyone here. I followed along at first and eventually started to post whenever I thought I could add something. I think it is important to have people in your life who can understand exactly what you have to go through. Their are challenges that are unique to Lupus patients and also those that are unique to anyone with chronic illness and it helps to have others who get it. You are not alone and hope you will never again feel that way.

April

Yesterday I dared to Struggle. Today I dared to win- Bernadette Devlin
When you get to the end of your rope, tie a knot and hang on-Anonymous

04/15/2011 09:57 PM  Top
mumeva
mumeva
 
Posts: 5494
Group Leader
I'm an Advocate

This group has been a big blessing to me.....it came at a time in my life where I thought I wasn't going to live and when I signed up for this group I found so many wonderful and caring people who truly understood me.......82nd.....were all on this journey together and we all make a difference in each others lives.....This is an amazing group of people.

Eva

I long to dwell in your tent forever and take refuge under the shelter of your wings: Psalms 61:4

04/16/2011 01:14 PM  Top
Bunnyhugger75
Bunnyhugger75
 
Posts: 2019
Senior Member

Very well said! This group has had a significant impact on my life too. I have made lifelong friends here. You all have been here for me every time I needed you! Even though I may be absent for a while, everyone invites you back with open arms. It makes all the difference in the world to share with people that go through the same rough times!

Amy

Diagnosed with Lupus in 2002. 36 yr old On: Plaquenil 2x a day, Cellcept 500mg 2x a day,Lasix 40mg 1xday, Prednisone 9 mg, Folic Acid 1mg, Vit D, Prilosec, Effexor 50mg 2x a day, Ativan 4 mg a day, DHEA, Methadone 2xday, Dilaudid 4mg, compazine, Imitrex, Doxepin,phenegran all as needed (prn).

Other diseases: Adrenal Insufficiency, Endometriosis, Crohn's Disease, Gastritis, Postherpetic Neuralgia, Raynauds, Sjogrens, chronic anemia, costochondritis, fibromyalgia.

04/29/2011 09:11 AM  Top
J3man
J3man
 
Posts: 280
Member

82nd...We all know the feeling. I think it is great that you found this group under the same duress and feeling of hopelessness as myself and many others here. I also was at my wits end and turned to the internet for help and support. This site was truly my last-resort and it quite literally saved my life and helped me turn things around for the better. I welcome you, "Big Bro'" I also would like to thank all here that have been helpful, supportive, and understanding. It was a rough start coming into this group for me and I am glad that the members here were patient with me and gave me a chance. It was difficult at times but I am soooo grateful for the encouragement that I have received to stay in the Group. Little Brother Lupus, Bryan

04/29/2011 03:23 PM  Top
zizzcat
 
Posts: 515
Member

This group is a blessing for me as well. I'm not able to participate as much as I would like but I try to keep up here and there. I'm also very greatfull to the leaders of the group for making everyone feel so welcome when they first start. I know that I felt very welcome and so it was easier to open up and share what was going on with me.

Hope


04/29/2011 07:30 PM  Top
Hakuro
Hakuro
 
Posts: 490
Member

And the magic of this group is that distance and time are no barriers!

Post edited by: Hakuro, at: 04/29/2011 07:31 PM

Carpe diem

05/01/2011 06:06 PM  Top
anonymus123
anonymus123
 
Posts: 54
Member

You are not alone.............
SLE, raynauds, seizures, arrithmia

ergocalciferol 50,000iu per week
plaquenil 400mg
meloxicam 15mg
cellcept 3000mg
topiramate 25mg
lexapro 10mg
metoprolol 50mg
prednisone 10mg
omeparozole 20mg
bromcriptine 5mg
ultracet37.5mg
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