Yes, I'm still here...
Well, well, well, she still lives! LOL! Yes, I do!
I cannot believe that it's been a MONTH since I've been on! I serious cannot …
is feeling Good
In 1993, I was dx'd with hypothyroidism (low thyroid), and in 1997, dx'd with migraine. Since 2001 I have been diagnosed with Fibro, Arthritis, Undifferentiated Connective Tissue Disease, Bronchitis, Degenerative Disk Disease, and all that those entail. The doctors think on and off that I might have MS, so maybe someday I'll be diagnosed with it, but not this week. It's like facing a huge rock mountain, that you have to climb everyday all over again, without being taught how to do it, or given the proper tools to do so with. I recently was referred to a Pain Management Clinic and my new doctor is AMAZING! She actually treated me! She believed my pain, she believed my illness, and she's treating me! My pain levels have gone from an 8 down to about a 1-2. But I finally have medicine that is treating and handling my pain. I will forever be indebted to this wonderful doctor. My family doesn't understand what I deal with every hour of everyday, but they try at least. There are days when I wish I could just disappear, but I do have responsibilities, so it's not an option. I live on a beautiful piece of property with wild animals (that keep picking my chickens off one by one). I love it here though. I wouldn't trade it for the biggest, most expensive house in the best subdivision in the world. It's home! Daily Strength came to me when I was about at the end of my lifeline. I thought that I was the most alone person in the world. I know that's not true now. I know that there are people, lots of people just like me! It helps alot to know that. I love my DS friends as if I've known them my entire life, and would do anything in my power to help them. I'm a caring, loving, nurturing, motheristic type person. I'd do anything I can to help anyone. Not trying to sound conceited, just what I've been told. When I love, I love deeply. I love unconditionally, but expect the same back. Conditional love = fake love. I run a chat room for people with illness like Fibromyalgia, Chronic Pain, Chronic Fatigue Syndrome, Insomnia, etc. pretty much anyone who needs support. Please feel free to drop in anytime. We try to always have someone in the room, so no one feel left out. It's a loving place, no arguing, lots of support and just a great place to relax and have some fun, but also get some answers. The address is: www.xat.com/FMSupport But it's not just for FMS. Just had to pick a name. I'm from Texas and I'm allll Texan! Until you've lived here, you don't know what heaven is, so ya'll all come when you want to know what REAL life is!
My Lord and Savior; my family; my church and church activities; reading, especially true crime; my 'puter; crocheting; counted crosstitch; my online support groups; my AMAZINGLY WONDERFUL DS friends; watching movies/t.v.; and anything that I can do, without moving too much. But before I got sick with fibro, I loved camping, swimming, trampolining with the kids, b-b-qing, LOVED-cooking and baking, roller skating, bicycling, etc. Now that I'm feeling so much better, I'm hoping to get back to most of all that. I still have to be wary of my back, but lookout kitchen, because momma's coming back! Whoo!!! Hooo!!!
Well, well, well, she still lives! LOL! Yes, I do!
I cannot believe that it's been a MONTH since I've been on! I serious cannot …
I have one of the most "memorable" New Year's Eve's of my life, if not THE most memorable:
I haven't gotten fireworks for …
Well, I'm back from this "lovely" Christmas trip. Let me enlighten you to how fanstically it went!
We got to my grandmother's …
just sending this to let you know im still here and praying for you my friend hugs Sandy
Always © By Brandon A. Swaggerty The day you were born, the whole world was blessed These thoughts in my mind to you I must confess The time has come for me to express my true feelings You are the center of my thoughts and the essence of my being What you have brought me I never thought I could procure The gift of comfort, with you I am secure For you have lifted me up from a life filled with sorrow And made me realize there is always a better tomorrow It amazes me how someone can make me feel this way I love you more and more with each passing day You brighten my days and lift my spirits I have felt this for so long and now want you to hear it So you may know the place you hold in my heart You are always with me even when we're apart I truly believe what we have is meant to be Just open your heart and soon you shall see What I am willing to do to keep a smile on your face Just know that I'm here and will be always
Hi there, how ya doing? Hope you're having a great day!
happy 4th july!!!!! xxxxx
hi honey,sorry for absence.hope you are doing well.take care xxx Terri
Since 1993 I have been diagnosed with Hypothyroidsim, Fibro, Arthritis, Connective Tissue Disease, Bronchitis, Degenerative Disk Disease, and I list them all here, because their all autoimmune disorders/diseases. Fibromyalgia has taken away my life, my identity, the very essence of who I was. I no longer remember the old me. I've "Kissed Her Goodnight". Now there's a new me. I've yet to learn if she's a better person. But know she's more compassionate, and more obedient to God.
I am a mom and wife dedicated to my family in an Interracial Marriage. My husband is from Mexico and I am Caucasian. It causes us many, many problems on a daily basis. But we are dedicated to each other, and know that we can work through any problems that arise.
I have struggled all of my life. I hit my all time high of 240 a couple of years ago. Over the last 2 yrs. I have been losing slowly and have lost around 60+ lbs, and hope that I haven't stalled there for long. I don't find that any particular diet is necessary, or excercise, I just only eat when I am hungry, and I eat just enough so that I am not hungry anymore. I eat anything I want, just don't over indulge (except now and then). I hope to eventually get to my "ideal" weight but we will see.
I have arthritis among other things. I am a SAHM, married, in the country. Wish that I could enjoy all the things that my brain wants to do, but my body won't allow me to do.
Have degenerative disk disease in L3, L4, L5 and S1. About every six months, I bend over and out my back goes. I am down right now. It is so ridiculously painful! Childbirth was a cakewalk compared to this, and I didn't have an epidural with any of the 4 deliveries. Absurd! NOW I have to have epidurals. The irony!
I have FM, arthritis, hypothyroidism. Hydrocodone HELPS, but doesn't take the pain away. Sick of docs who care more about what they look like than actually HELPING their patients. Fed up with the medical establisment completely.
I have chronic pain and so it is depressing. Some days are worse than others, but I know that I just have to deal with it. Maybe someday my situation will improve, but doubt it.
Well, I feel that I'm pretty good in this area but there's always someone better to learn from.
No Dx yet. Doc thinks I might have it. Looking for answers to my symptoms.
I have had problems sleeping all my life. I remember being a kid, and waiting for the A/C unit to blow so I could fall asleep to that. If I don't have meds, I don't sleep, end of story.
What female DOESN'T have sexual issues.
I generally have two phobias. I have an EXTREME fear of scorpions, that leads to a panic attack (hate even saying or typing the word!!!!) and claustrophobia. For example: I can't STAND to be in the backseat of a car, in the middle. I just realized last week how insensitive and oblivious to this disease people actually are. Oh, the stupid remarks I heard! "You'll get used to it." Please, how moronic!!!!
I don't get PA very often, but if I see a scorpion, I definitely go into one! I haven't ever been on anything for it, so we'll see what I can get for them. They are very upsetting to say the least.
I just found out in 2007 that the reason I was having so many disc problems was due to DDD. It's is very upsetting, because there's not much I can do to stop the disease, as far as I know.
I actually have UCTD, but don't see a group for it. Of all of the diseases I have, this one seems to be the most aggressive and most painful of the bunch. It can get through the pain meds, and hurt me to the point of tears.