Guest guest Posted July 12, 2002 Report Share Posted July 12, 2002 Welcome, Mache! I'm glad you jumped in right away (she subbed yesterday!). That's the best way to go. :-) I must ask -- how do you pronounce your name? I'm Jacquie, the group moderator. My son, , has a dx of " autism/pdd " (which seems an oxymoron to me), and he'll be six on August 28. He's an only child. We live in Ontario, far far away from family and support. <sigh> This group is a real lifeline for me! What's you son's name? Where ya from? Jacquie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2002 Report Share Posted July 12, 2002 Hello Mache, I am Lori, I don't get on much but I do try. You will enjoy this list they are great support when you need a shoulder or anything else. Lori newbie Hello, I'm new to the group and just wanted to introduce myself. I have a 4 and half year old son with autism. He is still non-verbal but babbles all the time. Anyways, I'm happy to be part of the group. Regards, Mache Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2002 Report Share Posted July 12, 2002 Welcome, Mache! I'm Sara, SAHM to (aka Mikey) who will be 3 in September & has been dx'd with autism since his 2nd birthday. (Happy birthday!) We also have (Gabe) who just turned 1 in May. Oh, there's a husband and father here too, his name is Matt. And that's us in a nutshell. This is a very busy group but feel free to jump in anywhere and delete anything. How DO you pronounce your name, and what is your son's name? -Sara. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2002 Report Share Posted July 12, 2002 Hi Mache. Nice to meet you. I am Tamara. My daughter is 4 and a half too. She is autistic, ADHD, and bipolar. She is also still non-verbal, though she babbles a lot. Great to have you in the group..... Tamara --- Mache wrote: > Hello, I'm new to the group and just wanted to > introduce myself. I have > a 4 and half year old son with autism. He is still > non-verbal but > babbles all the time. Anyways, I'm happy to be part > of the group. > > Regards, > Mache > > ===== Tamara mom to : Ebony, 4 yrs -- asd, ADHD, bi-polar , 1 year wife to: Terry, love of my life __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 12, 2002 Report Share Posted July 12, 2002 Mache unsubbed without a word. <shrug> Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 13, 2002 Report Share Posted July 13, 2002 Nice to meet you Mache! Where are you from??? Welcome to the group! Penny Mom to Jacqui, 7 1/2, HFA Jeff, 19 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 4, 2008 Report Share Posted November 4, 2008 Nicki, I am a patient with Chronic Regional Pain Syndrome also know as Reflex Sympathy Dystrophy Syndrome. To make it easier, I will refer to the common abbreviations which are CRPS & RSD. I was the one that was concerned with the fact that my pain was so severe but that the surgery I just had was suppose to make me feel better. That is when I was concerned that my orthopedist was going to think that I was having something going on in my head. My surgeon is young & I believe that it is a God send to me that it allowed him to remember patients he had observed during his medical training. He knew after the third or fourth time after I went into his office crying in severe pain & nothing could soothe me. He also had an assistant in the room that said the fact that I had RSD. That was a new one on me. I'ld had never heard of this disease before. Hopefully, if your doctors already mentioned chronic pain syndrome to you, the doctors are already planning on what they need to do to ease your pain. >Nicki wrote: Hello everybody >My name is Nicki I'm 35 and I come from Guildford, Surrey. I have suffered from lower back pain for many years. I have had 5 procedures carried out on it consisting of facet joint injections and RF all to no avail. I'm beginning to think that the professionals think I have chronic pain syndrome and that I'm imagining it which really frightens me and leaves me feeling very alone. It would be nice to hook up with others who are going through the same experience. Nic x Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2009 Report Share Posted January 6, 2009 Hello, I've been living with chronic pain for almost a year now. I've been to quite a few doctors. I used to have terrible burning pain all over my body. My general doctor put me on Cymbalta, and my neuro has me on Gapbentin 1,200 mg 3x a day. Most of the burning pain went away. The only problem I have now is some intense itching in my thigh area. Once in awhile I'll have a pins and needles feeling all over. My abdomin always hurt on the left side. It really hurts if I press down on it, sometimes it takes my breath away. I also have a pulling sensation bilateral by my pelvic bone, and it feels raw always on my pelvis. I've been tested for every disease possible, had a whole body MRI, EMG, and EKG, and all test come up negative. I really wish I knew what is going on. I would love to return to work soon and start living a normal life again. It's really unfortunate that with the technology we have today nobody has a clue what is happening to me. If anybody has similar symptoms please contact me, or at least help me learn how to cope with this. Some days I just want to kill myself, not joking. Nikki Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2009 Report Share Posted January 6, 2009 Thank you soo much for your reply, I think I'm going to try the heat pad and massage, and I think it might be wise to ask my neuro if I should start seeing a pain specialist too, since this has been going on for soo long.. I think it's time to actually step up to the plate and do it. Thank you for your help Nikki Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 6, 2009 Report Share Posted January 6, 2009 You're welcome, and I hope you get things worked out, because we all want less pain, and the courage to deal with it in a positive way. > Thank you soo much for your reply, I think I'm going to try the heat > pad and massage, and I think it might be wise to ask my neuro if I > should start seeing a pain specialist too, since this has been going on > for soo long.. I think it's time to actually step up to the plate and > do it. Thank you for your help > Nikki > > > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.