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RickEJ"I was diagnosed 8 years ago with Bi-Polar II.
With no support in my area I searched the web for help, after two years I stumbled on to MDJ.
The bi-polar II group has been my life line since 12/26/2009.
dizzyb my friend, you are not forgotten!
RickEJ
" (RickEJ)

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FMS ForumsGeneral & SupportNew to Group...new to diagnosis
01/09/2010 02:18 PM
BabyDragon
 
Posts: 3
Member

Just wanted to say Hi and introduce myself.

I just got the " official " diagnosis yesterday, although I have apparently had fibro for at least 10 years now.

(sigh)

Now comes the fun of finding a medthat works I guess...I am on Salsate and starting Neurontin and Ambien next week.

Judie
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01/09/2010 02:26 PM  Top
broken
broken  
Posts: 9447
Group Leader

welcome to the group ( family) let me tell you ,you have found the perfect place..

I personally dont like neurotine because of the effects it gave me, I currently take gabitril.

I also take ambien and thought it a God sent,I really was confused because I slept so much but the doc exsplained my body wasnt in the right sleep..Im again glad you found us..

we all have alot to give if one gets the help then some of this suffering is worth it..

remeber I am not a doctor I just say what I think

01/09/2010 02:29 PM  Top
mammy
mammy  
Posts: 7217
VIP Member

Hi Judie and welcome to our family. You are going to love it here, I promise. You don't have to go through anything alone, we will be here for you. If you need to vent, feel free. If you have questions, we will do what we can to answer them. Usually finding the right med combo is one of the toughtest parts of fibro. Then you need to find a way to manage your life around it and not let it take over your life. It may sound impossible but it's not, you can do it. I look forward to getting to know you and please let me know if I can help with anything Smile
Connie

I am not a doctor and do not play one on these forums so please consult your physician for actual medical advice.

01/09/2010 02:33 PM  Top
MissStacey
MissStacey  
Posts: 14843
VIP Member
I'm an Advocate

Welcome to the group, it is so supportive here. Most of us that were diagnosed had known we had had been suffering with it for many years before so personally for me it was a relief to be diagnosed. It was putting a name to my pain and knew I could finally be properly treated instead of living in silent pain forever. We can all relate to you and are here for you. You are not alone in this. Keep posting and keep smiling! Stacey Smile
I suffer from Rapid Progressive MS, Lupus, Fibromyalgia, Epilepsy, Migraines, Neuropathy, IBS, Narcolepsy, Arrythmia, Arthritis and too much more complete list on profile.

"Just because we have the right to disagree with a person, does NOT give us the right to disrespect that person."

I'm not currently active due to many personal and medical issues. I will not be participating in MDJ for awhile, my thoughts and prayers are with everyone. I hope everyone is well and I appreciate all of the thoughts, kind words and messages. I have tried to respond as much as possible and apologize if I have not gotten back to everyone. Love & Hugs, Stacey

01/09/2010 02:39 PM  Top
Clarita
Clarita  
Posts: 10951
VIP Member

Judy, a most warm welcome to you to this fabulous dynamic group full of kind phenomenal individuals. Just know you will love it here! Has made a huge positive impact upon my life since joining last July, too, for sure!

We are all here for you so lean on us. Feel free to just be You. Vent when you need to vent. Ask for prayers if you need prayers. Ask questions that are on your mind. Just treat us like a family.

Let us know how the new meds work.

Have had fibro for 13 years this October, yet, determined to be free of this condition one day. Am an optimist plus a wounded warrior Wink Smile!

Take excellent care of you Judy. (i) Angels be with you (i) all this weekend, amen.

Warmest wishes winging their way to you- make sure you keep warm too, giant gentle hugs and much love all the way from Devon in the UK, Clarita Smile xooxooxoox untitled


01/09/2010 03:48 PM  Top
hatbox121
hatbox121  
Posts: 10654
Group Leader

Amy~ “When you come to the end of your rope, tie a knot and hang on.” ~Franklin D. Roosevelt

Current dxes-Ehlers Danlos Syndrome, Mitral Valve Prolapse w/regurg, 2 other heart valves with regurg, POTS, DDD, scoliosis, various OA, polyneuropathy of unknown origin, SI joint dysfunction/fusion/collapse, chronic rotar cuff tendonitis, impingement syndrome of the shoulder, chronic bursitis in various locations, degeneration of the sternum, vertigo, GERD, FM, CFS, CPS, various bone marrow lesions, brain lesions of unknown cause, migraines, TMJ, vertically bulging discs, Raynaud's, anemia, tinnitus, high copper levels, borderline glaucoma, colon polyps, intermittent RLS, Vit D deficiency, depression, Eye accomodation disorder, Essential tremor, recurrent kidney stones, sacral spine disorder, inflammed tendons, and inflammation of spinal nerves(no specific dx).

I'm am not a dr. I am not a substitute for a dr. All advice I give is based on research and my personal experiences.

Previous discussions I participated in:
Has fibro attacked your joints.
New to the group.
Newbie

01/09/2010 06:28 PM  Top
Auntie3285
Auntie3285  
Posts: 9113
VIP Member
I'm an Advocate

Hi Judie,

Welcome to our group ~~~ we re happy you ve found us.

It sounds as if you re on the right track in being dx d as well as starting meds for Fibro.

I have never taken any of what you mentioned but several here are/were taking Savella.

Please feel free to ask any questions you might have. This is the most caring support group you can imagine to find ~~~

Marilyn


01/09/2010 06:51 PM  Top
jenigood1
jenigood1  
Posts: 3311
Senior Member

...Jeni
Jeni

Lamictal
Abilify
Cymbalta
Trazodone
Vyvanse

"Remember - when you fall on your face, you're still moving forward!"
My advice is free, completely anecdotal, and comes from my own experience. Always talk to your doctor before you change anything.

01/09/2010 08:29 PM  Top
phire009
phire009  
Posts: 2157
Senior Member

Welcome Judie,

You've just joined one of the greatest "FAMILIES" on the site. Each and every guy and gal here are caring and compassionate and what ever you need just ask we're all here and everyone has had diff. experiences so just ask away.....Also getting the right med combo is the hardest thing it's all trial and error and may take a while but when find it things will get better. Not back to perfect but where you'll be able to relieve some of the pain....

Will be praying that you pain subsides

Blessings

Debi


01/10/2010 06:19 PM  Top
chloebon
chloebon  
Posts: 370
Member

HHHiiii JJJuuuudddyy. WWWaaarrrmmm wwweelllccoommeee fffffrrrooommm sssuunnnyyy ffffllllooorrrriiidddaaaaaaa!!!!!!!!Sorry for your diagnosis, but at least now you can start trying meds to see what combo will help your pain. It really is a hit and miss with the fms. I take the neurontin (I helps a lot) along with muscle relaxers and pain meds. I do not do well with the sleep meds. I have night terrors as it is and the sleep meds only enhance them. Welcome to the group, you will find understanding and companionship here. Everyone understands what your going through. You are no longer alone. I know you are warmer where you are (the cold makes it worse). I hope to have waarm weather by the end of the week. Glad to meet you. Good luck with your meds.
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