Newbie....looking for friends who understand

New Topic Post Reply Printable Version
28 posts in this thread.
Viewing Page :
 1  2 
[ << Previous Thread | Next Thread >> ]

antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/27/2010 9:38 AM (GMT -7)   
I originally posted this on the RA forum.....but basically all I know that I have , for sure, right now is chronic pain.....Where to start......well...in 2007 I slipped on ice at work, I did not fall but I twisted hard and weird and hurt my lower back. Long story short...I was dealing with workman's comp docs who could really care less and the only real diagnosis I got was a non-specific problem at L5-S1. I basically got released with no follow up after 2 months off work and was told it would get better on it's own. It never did and I was afraid of losing my job, and thinking that maybe it hurt because I had been off work for a while, so I kept it to myself and suffered through with vicodin. Well, the job fired me anyway and now 3 years later I am suffering worse! I have lower back pain all the time, when it is at the best it gets, it is still about a 3. I have pain that comes and goes in my hips, rear, thighs, knees, feet, neck, shoulders and head! I have nerve stuff going on all the time....it feels like I have spiders crawling all over my legs and muscle twitches. I am now on MS-contin and cymbalta. Prior to getting hurt, I worked double shifts as a waitress at a busy restaurant and worked as a finisher for a home builder where I was on my feet on concrete for ten hours a day! Now I can not stand for 1 hour....or sit or lay down without pain! So, this has been my life for 3+ years and then 2 weeks ago.....bam....got hit with something new!! It was a Thursday morning at around 2:30 am...I woke up hurting which is nothing really new but this was different! I also felt like I was running a very high fever. I put sweats on and crawled back under the blankets and I was shivering all over. This is very different for me because I usually get very hot when I sleep and I was freezing! I was able to go back to sleep but figured I was going to wake up very sick. I woke up again at 5:00 am and did not feel sick really, other then every single joint in my body hurt so bad I wanted to cry! I have only had actual "joint" pain on rare occasions. And I had a terrible earache! I figured it was the ear infection that caused the fever at 2:00 am, but I had no fever at that time. I tried putting peroxide in my ear but I got no results....it would not go into my ear. My wrists, hands and fingers hurt really bad and were swollen. My knees were killing me, my feet hurt and my neck and shoulders were so stiff. I also had a headache. The MS-contin was not touching any of this pain!! I finally decided to go to doc on Friday because the earache was unbearable and the joint pain and swelling was not improving either. I also had a weird lump on the top of my arm above my left wrist. When I got there the doc looked in my ear and said, to my surprise, "there is no infection, your ear isn't even slightly red." She discussed the possibility of TMJ and was a little worried about polymyalgia rhuematica. Because I do not have insurance right now, she decided the most cost efficient thing to do was a SED rate. I had not had one since 2006, when my rate was 11. Her concern at the time was the polymyalgia and she said if it was that my SED rate would be sky high. She gave me a steroid shot and some oral steroids and said let see what the SED rate shows. She called to tell me the SED rate was moderate, that it was 53, but she felt better about it not being polymyalgia. So I was told to take the steroids and we would go from there. Well it took about 3 days but I finally felt better.....well better from that and was just back to my "normal" other pain. Now I have tapered off and will take my last steroid today and I am scared to death!!! I am starting to get a little achy, the lump above my wrist is coming back and I just have a general sense of doom! Also, I forgot to say I have been totally exhausted. I don't sleep for long periods at a time because I hurt, but I feel like I could sleep all the time! I am looking for some answers because it seems like my doc was so concerned about the polymyalgia she was not looking for other things. My sister has belonged to this forum for a while....well the fibro and the migraine. I have spent a lot of time here reading, mostly in the chronic pain until this last episode then I came to the RA forum. Can some of you share what your flares are like, or your first flare that brought on your diagnosis. Also what is a "normal" SED rate for RA? I am just looking for some help.....thanks for reading! It is nice to have people who understand to vent to! Bless you all on your personal pain journeys!

Retired Mom
Veteran Member


Date Joined Feb 2010
Total Posts : 1753
   Posted 5/27/2010 10:25 AM (GMT -7)   
Hello and welcome.

I don't have an answer for you and certainly can't give medical advice, but I have fibromyalgia (along with a ton of other things) and I wonder if you have had a fibro flare to go with your back problems. It can certainly cause widespread pain and joint problems. I would suggest an internet search of fibro to see if that might be a possibility. Many of us here can attest that fibro is not something to be taken lightly and that pain from it can be really bad sometimes. We also find that we are human barometers and can tell when the barometric pressure is changing before the weather man can. Low pressure = high pain levels.

Best to you and again, welcome to the CP board!
Retired Mom


antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/27/2010 11:16 AM (GMT -7)   
Hello,
Thank you for responding...I feel so lost! Having a bad pain day today! I can certainly relate to the pressure affecting the pain. I started putting that together a couple of years ago and about 9 times out if 10 when my back is really bad, the pressure is low or falling! I have read a lot about fibro also, my sister has it. She is the one who brought me to this forum. My sister is "damouthy1" and has fibro and migraines. She lives with me which is a blessing because we have each other to lean on! I guess I was kind of leaning away from the fibro and towards the RA because of the SED rate, the inflammation and the "lack of" pain at the fibro trigger points. The bad "earache", which was actually pain and inflammation in my jaw joint, was also a symptom of RA. I have no insurance right now and I am so broke! I just want to know what is wrong with me!! I am feeling so lousy today and I am starting to panic because I am now done with the steroids!! And of course the depression feels like it is consuming me! Thank you again and bless you! Take care of you!

damouthy1
Veteran Member


Date Joined Sep 2009
Total Posts : 663
   Posted 5/27/2010 11:40 AM (GMT -7)   
Hey Sis! I am glad you finally broke down and signed up! I hope some of the regulars come on soon and welsome you, I think you will like it here. Love you!
Gentle Hugs,
Shannon
 
Fibromyalgia, Chronic daily headaches, Migraine disorder (with and without aura), GERD, High blood pressure, Depression and Anxiety
Oxycontin, Flexeril as needed, Lopressor, Lexapro, Omeprazole, Clonazepam as needed, Promethazine as needed for nausea from migraines


White Beard
Forum Moderator


Date Joined Feb 2009
Total Posts : 3611
   Posted 5/27/2010 1:27 PM (GMT -7)   
antbuggey

Welcome to Healing Well Chronic Pain Forum, you know we are not Docs here and we cannot fix or diagnose your problems, but we all have something in common, and that is Chronic Pain, we all know what it is like to live and exist with CP, so when you come here to this forum, you can be assured that you are not alone in dealing with CP, and I think, and I hope that you will find the people on this forum to be the most caring, and supportive, and compassionate people that you will find anywhere on the internet! I know that I certainly think that they are! I consider everyone "Family" to me! I hope that you will stick around and post and also join our "family"! And even though we cannot fix or diagnose you or give you medical advice, we can give you our ears and listen to you, and we can and willl give you compassionate and caring advice and support, and share in your burden of living with CP! You are never alone with your pain when you are here on the forum!

Again I Welcome YOU to our "Family"

White Beard

straydog
Forum Moderator


Date Joined Feb 2003
Total Posts : 13470
   Posted 5/27/2010 1:27 PM (GMT -7)   
Hi AntBuggey and welcome to the CP forum. I am glad that you decided to pop over and check us out, but very sorry you have to be here. All I can tell you is I have suffered over 20 years with this mess and as more time goes by so does the the pain. I would like to ask you if you have actually been dx'd with RA or not, that part I was not clear on? Not having insurance makes it very difficult to get medical treatment unless you are eligble for state funded insurance like Medicaid or something along those lines. I know for instance in Tenn, they have a program called Tenn-Care that is available. Each state is different but all do have Medicaid. Without a dx from a dr anyone could say it could be one of 100 different things which gets you no where except more upset in not knowing really what the problem is, so I would tread lightly on asking people what they may think is wrong with you, because none of us here are drs. Also, not everyone has the exact same set of problems associated with different medical problems. If you will look at CP 101 there is a lopt of good info there for people without insurance and there may be something there that can help you out.
 
I have a sister with RA and she is on steroids for the pain. She has terrible health problems and her dr is too afraid to try her on any of the drugs like Enbrel, Humira and drugs in that class. It is sad because those particular drugs really help folks with RA. She does a lot of self help things like tub soaks, hot showers and uses different rubs. She has lost almost complete use of an arm now.
 
I wish I could offer up something that would help you with this situation. Just know that you aare not alone with youer suffering. I think its wonderful that you and your sister live together. At least having her there with you, you are not alone. I have always been told misery loves company and I believe it, lol. At least you can come here and talk to others, vent if that needs to be done and know that everyone understands how you feel. It is just not fun having pain all the time.
 
I am sure the others will be along and will pop on and tell you hello and welcome aboard. Take care and keep posting and let us know how you are doing.
 

crohns disease dx 2002 & small bowel resection, still looking for remission whatever that is, chronic pain 22 yrs, added ulcerative colitis 6-05 to the mix, high blood pressure 28 yrs, aortic heart valve insuffiency, depression, osteoarthritis, osteoporosis lumbar spine, scoliosis lumbar spine, peripheral neuropathy hands & feet, COPD & on oxygen therapy, lupus & psoriasis and psoratic arthritis. Several other health issues just not enough room to list it all. Too many surgeries to list and too many medications to list. Currently on 17 different daily medications. Intrathecal pain pump implanted June 05.


antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/27/2010 2:41 PM (GMT -7)   
Thank you White Beard and straydog for responding! First off, please know that I do understand that no one here is a doc and can not give medical advice. I am very sorry if my post seemed to come across like I was seeking medical advice. I am just having a bad day....very anxious...and wanting answers. Straydog, as of now, I have not been diagnosed with RA. These problems just started a couple weeks ago. I have had chronic pain in my lower back with nerve impingement for 3 years but the other stuff is new. Because of the lack of insurance the doc did a SED rate test which is relatively cheap....that was high....53 and normal is under 20. Her biggest concern, and the reason for the test was because she thought it could be polymyalgia rhuematica. However, that would have shown a SED rate in the 100's, so the doc felt better about that and said to just take the steroids and we will go from there. I felt like because she was so worried about the other that she kind of overlooked just how bad I was feeling!! The pain I was in was overwhelming and I am afraid that now that I have taken my last steroid....it is going to come back.....over the weekend when I can't get help! I guess I was just looking for some answers as far as what people have experienced...as far as the first onset of RA......the more I read the more I relate to what is said about RA. My sister has been on here for a while and I am glad I finally came aboard......Pain certainly makes you feel alone sometimes!

Thanks again and I hope to be on here a lot......

To All........Take care of you!!
Beckey

White Beard
Forum Moderator


Date Joined Feb 2009
Total Posts : 3611
   Posted 5/27/2010 10:34 PM (GMT -7)   
Beckey

Steroids can really make a difference in pain if it is caused by inflamation, ususally the relief that you get from taking the steroid last for at least a little while after going offf of them, it is not like when your are taking a pain pill and when you quit taking them the pain comes back. Now I am not saying that your pain will not return but usually with steroids it takes a while for it to come back, because the inflamation has to come back, that is why when they give epidural steroid injections into your back that they usually last a little while, some get relief for months and months, others like myself only get a few days or weeks from them.

Anyway when you are frustrated and need to vent, you know we are right here to listen, and give you support! So many times when your in pain you feel like you are the only one in the world that feels that way! and it is a very lonely feeling, at least that is how I am sometimes! But your not alone here!

I do hope you have a Great weekend Beckey!!!

White Beard

antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/28/2010 7:21 AM (GMT -7)   
Thanks White Beard....that helped! I was afraid that my holiday weekend was doomed to just fade away to pain! I know there is not a guarantee I won't have pain, but it is nice to hear that it may not just come back full force like it was!

Have a wonderful weekend and take care of you!!

Beckey

MIKEL99
Veteran Member


Date Joined Feb 2010
Total Posts : 914
   Posted 5/29/2010 4:52 AM (GMT -7)   
Hi antbuggey , just wanted to welcome you to the family , I'm sorry I don't have advice to offer , but I do offer my support . You will find folks here who will always listen to you , whether you need to vent , explain or whatever , we'll try to offer advice if we can but you can always count on emotional support , welcome friend ! Mikel

antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/29/2010 6:06 AM (GMT -7)   
Hello Mike and thanks for the welcome! I am very happy that my journey has brought me here! When you feel like no one can possibly understand and you are so alone.....it is nice to find a safe place! My husband is an incredible man and does his best to understand and I think that makes it even harder for me sometimes! I feel like my pain is not only ruining my life but his too! I feel guilty for always whining about how cruddy I feel and putting that pressure on him, so again, it is nice to find a place where people really do understand! Thanks again and take care of you!
Beckey

Chartreux
Veteran Member


Date Joined Aug 2006
Total Posts : 9622
   Posted 5/29/2010 6:57 AM (GMT -7)   
I would say to aask for bloodwork to be done to check for the RA...as it would show up on bloodwork...ANA testing...ANA is for the inflammation markers, I don't know what a sed test is..
sorry...Have you had any MRI's done of your back or any nerve testing called an emg??? just wondering...
My pain cames from a car accident...I sure hope your doctor can find something out...RA can be wickedly hard on the body, my grandmother had that...would a heat pack help..
some of us use heating pads or ice packs to help with our pain...and a good pain management psychologist can help you learn some relaxing techniques..
Nice to meet you, but sure wish it was under better circumstance other than chronic pain...
((((((((((((((((((((((((antibuggey))))))))))))))))))))
hugz

straydog
Forum Moderator


Date Joined Feb 2003
Total Posts : 13470
   Posted 5/30/2010 10:19 AM (GMT -7)   
Antbuggey I hope you are having a decent weekend. I know you were concerned once you took the last steroid your horrible pain may return. Since they sort of build up in your system you should be ok for a bit longer.
 

crohns disease dx 2002 & small bowel resection, still looking for remission whatever that is, chronic pain 22 yrs, added ulcerative colitis 6-05 to the mix, high blood pressure 28 yrs, aortic heart valve insuffiency, depression, osteoarthritis, osteoporosis lumbar spine, scoliosis lumbar spine, peripheral neuropathy hands & feet, COPD & on oxygen therapy, lupus & psoriasis and psoratic arthritis. Several other health issues just not enough room to list it all. Too many surgeries to list and too many medications to list. Currently on 17 different daily medications. Intrathecal pain pump implanted June 05.


antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/30/2010 12:00 PM (GMT -7)   
Hi straydog and thanks you for the well wishes...I hope you are having a good weekend also! So far the terrible pain in my joints has not returned....thank goodness! I have had a couple of really bad back days, spent most the day in tears yesterday and still pretty achy today, but my back stuff has been around for 3 years and I have bad days and pretty good days, as far as that goes!! My biggest problem the past 2 days has been terrible fatigue!!! I just want to sleep all the time and seem to keep myself from doing just that!! Kind of a waste of the weekend and I feel bad for my hubby, but I am not hurting like I was afraid of! Anyway.....enjoy your weekend and take care of you!!

Blessedx8
Veteran Member


Date Joined Aug 2008
Total Posts : 3193
   Posted 5/30/2010 12:44 PM (GMT -7)   
Hi Antbuggey (Becky)...

First, welcome to the board :) I'm sorry you are dealing w/ so much... but glad you found your way here. There's lots of wonderful people here who really understand what it's like to live w/ chronic pain and health issues. I hope to get to know you better... I'm glad you have a supportive sister and husband... it makes a difference, definitely.

I have lots of medical issues, too, and - over the years - have dealt w/ many of the things you are describing. I have had a high SED rate for many years... I don't know what the highest has ever been, but it's never gone below a 35. I've had the high fevers, chills, joint pain and such...but the chronic fatigue is the worst. And I don't have RA. I have autonomic dysfuntion (nervous system disorder); fibromylagia and a host of other junk. Anyway, I'm not sure what's going on with you - but I sure hope you can get some answers. Sometimes, the "not knowing" is the worst.

I hope you feel better... and I hope you keep posting and sharing. Take care of yourself... --Tina
Main Health Problems: Dysautonomia/POTS; CFS/Fibromyalgia; Severe Chronic Hypertension; Hypothyroidism; Hypoadrenalism; Mixed (Obstructive/Central) Sleep Apnea - on Auto BiPap; Depression/Anxiety; Severe Vitamin D Deficiency

Pain Issues: Cervical/Thoracic back pain (they called it DDD...but I don't know); migraines; carpal tunnel syndrome; widespread joint/muscle pain, nerve pain in hands/arms/feet; Future Plans: Intrathecal Pain Pump; already completed trial (Sept, 2008); awaiting my decision for implantation...


antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/30/2010 2:15 PM (GMT -7)   
Hi Tina and thanks for responding....I am really happy to be here (this forum) I just woke from, yet another, nap and this is the first place I went! It already feels like family here! I am very thankful for my sis and husband!! My sister truly understands because she is dealing with fibro and migraines...for the most part with other things thrown int the mix. My husband is just a wonderful man, I feel so bad for what my pain has done to him....and us! I have begged him to leave me but he won't! Sometimes it is just in fun, but other times I really feel like he would have a better life without me! Not only does my problems keep us from doing a lot of things but, at times, it just makes me grumpy and mean! I have always been a very happy, compassionate and kind person and lately....wow....I am mean! I hate it! Hopefully, I will get some answers soon and start getting some meds to help all of this!!

Have a great day and take care of you, Beckey

White Beard
Forum Moderator


Date Joined Feb 2009
Total Posts : 3611
   Posted 5/30/2010 10:00 PM (GMT -7)   
Beckey
I am sure that you still are that happy, kind compassionate person! it is still inside you! even with your pain, maybe just coming here and venting some of your frustrations, and knowing that when your here your among friends that do understand and care what you are going through, maybe, just maybe that ""mean"" ( as you say) in you, is really just your frustration with your Chronic Pain, and venting and sharing that with all of us here just might be enough relief for you from that burden that , that happy, kind and compassionate person can come back out, for you, and your husband and loved ones! It is possible you know. Of course getting a diagnosis and treatment is the best thing, But it helps when you can have a place to go such as this forum for a listening ear, and understanding, and compassionate support!

White Beard

antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/31/2010 10:13 AM (GMT -7)   
Thanks White Beard!! Thanks soooo much! I really needed that!! I am not that mean hateful person that has been hanging around here! I just gotta find me again and quit surrendering to the pain! I am also a fighter and I need to remember that!

Take care of you!!!
Beckey

straydog
Forum Moderator


Date Joined Feb 2003
Total Posts : 13470
   Posted 5/31/2010 12:06 PM (GMT -7)   
Aw Beckey I become just unbearable when my pain is out of control. It happens to all of us. Its really hard to be a sweet nice giving person sometimes when all you want to do is scream at the top of your lungs trhat you are in pain and feel like crap, lol. I am having a rotten weekend because I live in Texas and the furnace has been turned on here way too early. It is hovering around 97 and has been for the past few days making it impossible for me to get outside unless I am in the pool. I hate it when its this hot. Its just awful. Plus my pain medication causes me to have awful sweats to top it off. Of course the AC is running non stop and the cool air from the AC tends to make my joints hurt. A real catch 22, lol. I am so tired of being inside I love being outdoors that I may break down and just sit in the pool for awhile.

Take care.
 

crohns disease dx 2002 & small bowel resection, still looking for remission whatever that is, chronic pain 22 yrs, added ulcerative colitis 6-05 to the mix, high blood pressure 28 yrs, aortic heart valve insuffiency, depression, osteoarthritis, osteoporosis lumbar spine, scoliosis lumbar spine, peripheral neuropathy hands & feet, COPD & on oxygen therapy, lupus & psoriasis and psoratic arthritis. Several other health issues just not enough room to list it all. Too many surgeries to list and too many medications to list. Currently on 17 different daily medications. Intrathecal pain pump implanted June 05.


antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 5/31/2010 12:33 PM (GMT -7)   
Thanks Straydog, I have only been to Texas once and it was the end of July for a wedding....wow...It felt like the air was so thick that I was unable to breathe and almost panicked. I am originally from Colorado, born and raised there, but moved to Nebraska 6 years ago. The area we are in is very high humidity and after six years I am still not used to that!! I will take dry heat anytime! I am on ms-contin 3X a day with morphine IR as needed so I can sure relate to the awful sweats!!! I sweat so bad around my hairline that the past few days, it seems like my hair never dries!! I wake up several times at night and my hair looks like I just washed it! I hate it...it is quite embarrassing! My sis and I joke that it is time to take a shower.......all day!!! LOL!! I thought it was hot here already, but, my goodness that is terrible!! I am sorry that you are so miserable! So far the AC does not seem to bother me, that stinks that it does you! Go enjoy the pool for a while....sounds like you need and deserve it!!

Take care of you!
Beckey

straydog
Forum Moderator


Date Joined Feb 2003
Total Posts : 13470
   Posted 5/31/2010 5:17 PM (GMT -7)   
I went out and got in and it felt great, first time in this year and I was surprised how at how warm the water is already. But, like I said we are having such awful heat right now it really warmed the wateer up quickly. I had spoke to my daughter this morning and asked if her pool was warm yet, she said oh yes and had been for a bit. I sat on the steps and it kept me plenty cool. I know after a shower sepsecially I will really have a round of the sweats and I do not use hot, hot water as it will drive my BP up. I knew the ground was much warmer because I am not having to turn the hot water knob over near as much. Drying my hair is something else, I wear it short, so I am sweating on my head as I am trying to dry my hair, lol. It does get embarrassing when out in public, especially in the winter when everyone is looking at you because you are having a meltdown and water is dripping off of you. I always use Viva paper towels as they absorb very well and do not disintegrate the minute they get I also get night wet. The night sweats are the very worst of the lot, I also get the night sweats with the crohns disease makes it a lot of fun. We have had a lot of humidity here already and I don't breathe well either in it. The air does get very thick with the high humidity.

Its after 7:00 pm my time and only dropped to 92, jeesh. Going to be a long hot summer.
 

crohns disease dx 2002 & small bowel resection, still looking for remission whatever that is, chronic pain 22 yrs, added ulcerative colitis 6-05 to the mix, high blood pressure 28 yrs, aortic heart valve insuffiency, depression, osteoarthritis, osteoporosis lumbar spine, scoliosis lumbar spine, peripheral neuropathy hands & feet, COPD & on oxygen therapy, lupus & psoriasis and psoratic arthritis. Several other health issues just not enough room to list it all. Too many surgeries to list and too many medications to list. Currently on 17 different daily medications. Intrathecal pain pump implanted June 05.


Pete trips again!
Veteran Member


Date Joined Nov 2006
Total Posts : 1899
   Posted 5/31/2010 6:57 PM (GMT -7)   
Hi Becke, I'd like to also ay welcome to our little cyber family! Sorry I'm a little late. I read all your posts and the responces everyone gave you. Sounds like you are well liked already! I also read what you posted on Chutzies post and was so impressed w/ your words there. I think you are gonna fit in here just fine and be a valuable voice here.
Your new friend,

Pete

antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 6/1/2010 6:23 AM (GMT -7)   
Hello Pete, so very nice to meet you! I have read MANY of your posts and what an inspiration you are....Thank you for the smiles! Also, thanks for the kind words you posted here! I am really glad to be here and looking forward to spending a lot of time here. Again, very glad to have now spoken directly to you and glad to have such an inspirational and amazing new friend!! There seems to be many amazing people here!
Take care of you,
Beckey

Pete trips again!
Veteran Member


Date Joined Nov 2006
Total Posts : 1899
   Posted 6/1/2010 4:19 PM (GMT -7)   
Holy smoke Beckey are you sure you are not mistaking me for someone else??? There are so many amazing peeps here> not me really!! I'm the goofy one of the family! It's my pleasure to meet you and I'm really glad you started posting!
A Big Hug from your new sillyman friend
Pete

antbuggey
Veteran Member


Date Joined May 2010
Total Posts : 594
   Posted 6/1/2010 4:54 PM (GMT -7)   
Awwww Pete, of course I was talking about you!! Every family needs a goofy one, and he is the one that EVERYONE loves! I do appreciate you and all of the other wonderful people here.....I think my meanness is even beginning to fade, and that can only be because of the wonderful folks on here!! I am very thankful for my new family!

Big hugs and take care of you!!
Beckey
New Topic Post Reply Printable Version
28 posts in this thread.
Viewing Page :
 1  2 
Forum Information
Currently it is Thursday, December 08, 2016 9:09 AM (GMT -7)
There are a total of 2,734,676 posts in 301,233 threads.
View Active Threads


Who's Online
This forum has 151347 registered members. Please welcome our newest member, Marie34.
341 Guest(s), 16 Registered Member(s) are currently online.  Details
sheepguy, Bololidat, BnotAfraid, Chanymom, mikeb2308, Mouche, Serenity Now, Loutucky, Tudpock18, iho, Healing98, Sallyyy, joavila92, houseboy, Mustard Seed, YiyiBoo


Follow HealingWell.com on Facebook  Follow HealingWell.com on Twitter  Follow HealingWell.com on Pinterest
Advertisement
Advertisement

©1996-2016 HealingWell.com LLC  All rights reserved.

Advertise | Privacy Policy & Disclaimer