Guest guest Posted January 5, 2004 Report Share Posted January 5, 2004 In high school I used to spend the night with a Philipino friend, and it is their tradition to eat last night's supper for breakfast the next day. The food was always so delicious and it tasted just as good or better the next morning. (They cooked pretty fancy dishes the nights I stayed over--I have no idea if they cook like that all the time.) jerilyn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 28, 2004 Report Share Posted January 28, 2004 Unsubscribe Welcome Hello! I the founder of a Russian-speaking forum h-longevity/ If someone from you knows Russian, I invite to us to join. Subjects similar. Good luck! Stanislav group email addresses: Post message: longevity Subscribe: longevity-subscribe Unsubscribe: longevity-unsubscribe Questions/Complaints: longevity-owner If you are interested in injectable growth hormone then we suggest you subscribe to Rejuvenation. Send a blank email to rejuvenation-subscribe Note: This forum is for discussion of health related subjects, but under no circumstances should any of the information published here be considered a substitute for personal medical advice from a qualified physician. The founder/moderator is not an MD, nor are many of the subscribers/participants. Also, advice and information presented here by MD's and other health care professionals should not be considered a substitute for personal medical advice. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2004 Report Share Posted April 23, 2004 , Your story sounded so familiar to me that I was compelled to write. First of all, welcome...and you came to the right place. Expect from these wonderful people; warmth, comfort, understanding, and humor. My heart problems began after the birth of my daughter (second child), went into cardiac arrest 10 minutes after she was born. When she was not quite six months old, I had open heart surgery. I remember the agony of not being able to hold her because of the weight restriction following surgery. It was later, after 1 pacing study, and 5 ablations that it was decided that I needed an ICD. The attempted ablations were unsucessful..I had VT also. I also needed a pacemaker because of bradycardia (too slow irregular heartbeats). i, like you, was young and a mother...scared out of my wits!! Way too much anxiety and fear was making me lose the precious moments of my daughters infancy. So, I focused on the good stuff, took some courses on stress-management and found some method of coping. Believe me, its not easy...and none of us here will try to tell you any different. Its a day to day effort.. The great news? You will recieve the support you need here from people who really know what it is like to live (not just exist) with an ICD. You are not alone. One day you will be writing words of welcome and encouragement to newcomers, telling them how you adjusted and are flourishing. Until then, enjoy each day and count your blessings.. Always, "Words are the voice of the heart" (Confucius) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2004 Report Share Posted April 23, 2004 , what a beautiful support letter and how well put. Sharon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 12, 2004 Report Share Posted November 12, 2004 Give us a bio, what do you eat, what is your workout like, and how do you want to change your life? The more we know, the more the members of this board will be able to help you. Thanks for posting. Stasia Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 10, 2005 Report Share Posted February 10, 2005 Hi Welcome to our little group. Lurking is fine but feel free to always chime in. We don't always talk about soaps & such as you can probably tell from all of our past postings. We're very informal here....help each other out when we can, support each other and lean on each other's shoulders many times whether it's business or personal stuff. So don't be afraid to " vent " about something if need be. You'll probably find that most of us have " been there, done that " , too. Upstate NY (smack between Syracuse & Albany) Re: Dyeing Herbs Hi, everyone. I've been a lurker here for a while (joined right before last year's gathering but didn't say much 'cause I wasn't able to come, and after that, I had family health issues to deal with back in the midwest, yada yada yada). But I wanted to chime in here. I've used alkanet root to color soap. It can be anywhere from blue to a purple to a reddish-pink, I think, depending on the pH of the soap mixture. Mine turned a lovely pastel purple color. I steeped the root powder in some reserved olive oil and strained it out before heating the oils. I've also used carrot, but I also added some powdered cinnamon, so my soaps came out kind of orangey-brown. That's what I use for a gardener's soap, great for scrubbing off the dirt. Haven't used any other herb or plant material that dyed the soap. Quick intro: I live in Macedon, just over the Monroe/Wayne Co. border. I have been soaping for at least four years (probably more, just can't remember), only CP, 'cause the first and only time I tried melt-and-pour it was a terrible failure for me. I also have made fizzy bombs and bath salts, and some deodorant for me. Some day I'd like to try my hand at lotions for me without preservatives, as I'm not too thrilled with the products I've bought in the stores. I have one son who just turned 7, and we homeschool. My hubby works at RIT teaching physics. I have only sold at two really small craft shows, a while back, but I never seem to have the energy to put into marketing, so we have a lot of soap around the house...! Take care, > From what I know of coloring with herbs in soap, with the > exception of calendula, it dosnt work so great. I have gotten a > very light > muted orange from using carrots and a greenish from using cucumber > but like > I have heard that using beets will turn brown. > > Maybe someone else has better experience at that? > > Shaye Be Impeccable With Your Word; Don't Take Anything Personally; Don't Make Assumptions; Always Do Your Best. - Don Ruiz Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 7, 2005 Report Share Posted March 7, 2005 Hi in IL. Wher at in IL. do you live? I am in fort, IL. I'm trying to find someone who lives close to me, that I can relate with. in IL.Laha1960@... wrote: In a message dated 3/6/05 5:53:45 P.M. Central Standard Time, Autism and Aspergers Treatment writes: When I'm there...I over-compensate and become "the life of the party". Some peope think I'm weird, and some think I'm just "out there" but witty and charming. But it's all sort of a learned ACT. I PREFER to be alone. I isolate. I FAKE social graces that I have learned to mimic VERY well...but somehow just don't fully understand. I feel like an actor in a play who doesn't fit the part. Same way at the jobs. I get confused easily. I forget what I've been doing...and I've been doing it for years. I have to RElearn everything I learned...coninually.Eventually....I lose it. Keeping this up for long causes emotional issues. Welcome to this list . I am , in IL. I have a son with Aspergers, and he is 16 in April. I am not Aspergers, not that I am aware of, but I am ADHD. What you descirbed above about yourself, IS something that I also have to deal with and have some trouble with as well, and I can honestly relate. I was really impressed with your love, wisdom and care for your daughter . That is wonderful. I am not sure if you are the custodial parent for her or not>? Anyway, good luck to you with her and keep up the great work and spirit of being a great dad for her. in IL Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 11, 2005 Report Share Posted June 11, 2005 Thanks for the welcome I am enjoying the group very much. I think the vacuum is created from the lack of air following the pah. I have noticed that if I suck up any air or don't get everything out on the pah I don't get the vacuum effect. Feel free to correct me if I am wrong ladies I am still only 4 days old at this. Mel > welcome to all the new members and Mel you will love this > group....so much inspiration. I do have a questionon the breath. > I've > read over and over about how it is a gentle breath and to relax. I > don't have any problem holding my breath but have been really > struggling with the sucking everything up and creating a vacuum part. > > It is an effort to do the breaths and I feel like I must be doing > something wrong or else I am just trying too hard. If anyone could > give me some ideas I would really appreciate it. Also Rashelle thank > you so much for all your interaction with the group. It is so > helpful. > > Chris Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 12, 2005 Report Share Posted June 12, 2005 On 6/11/05, pzuponu@... <pzuponu@...> wrote: > > I could easily lose 150 pounds but realistically > would love to get below 200. I would feel like a Barbie doll at 199!!!!! I feel the same way. My goal weight is 150 pounds but when (not if---thinking positively here!) I get below 200 I'll be estatic. I haven't been less than 200 pounds since before I was pregnant with my fourth child, and he's 19 1/2 years old. Sharon whimsicalscribe@... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 14, 2005 Report Share Posted November 14, 2005 Hi , Actually I probably should have him ask his oncologist these questions I'll write them down. He usually don't ask to many questions, thats why I'm trying to keep up with what he needs to ask. Especially last week when he had high calcium count. So far his treatment has been Leukeran and now they put him on predisone for a month. He has swollen lymph nodes, and they want to do a biopsy this week. I'll let you know what results are from the test. So far since he's been aware of CLL he hasn't had to many things going on other than night sweats, fatigue, and swollen lymph nodes. WBC are up and down with treatment. Thank you Donna jb50192@... wrote: Welcome, Donna Hard to say about your husband....... Do you live anywhere near where you could get an expert opinion? In some strange cases a second opinion can be invaluable. The high WBC by itself does not necessarily represent a danger. Important to know his lymphocyte percentage to compare with the white count..... Does he have swollen lymph nodes? Another thing to wonder about....... Let us know more, there are lots of people here with good theoretical knowledge...... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2006 Report Share Posted February 23, 2006 Welcome, richard! I bet you get a lot of Dick Van Dyke jokes, huh? Don't worry, it didn't even cross my mind! ;-) > > Welcome > > Van Dyke > Director of Safety > Summit Construction Co., Inc. > 1107 Burdsal Parkway > Indianapolis, IN 46208 > 317-634-6112 > 317-264-2529 fx > 317-710-6685 cell > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 23, 2006 Report Share Posted February 23, 2006 I've never heard that before. Just kidding. Would you believe my profession is that of Director of Safety? Probably working - because I have yet to trip over anything in the living room. Van Dyke Director of Safety Summit Construction Co., Inc. 1107 Burdsal Parkway Indianapolis, IN 46208 317-634-6112 317-264-2529 fx 317-710-6685 cell >>> erik@... 02/23/06 10:41AM >>> Welcome, richard! I bet you get a lot of Dick Van Dyke jokes, huh? Don't worry, it didn't even cross my mind! ;-) > > Welcome > > Van Dyke > Director of Safety > Summit Construction Co., Inc. > 1107 Burdsal Parkway > Indianapolis, IN 46208 > 317-634-6112 > 317-264-2529 fx > 317-710-6685 cell > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 21, 2006 Report Share Posted March 21, 2006 Hi Ya and Thank You for joining Us. So sorry to hear of all the added emotional and stressful problems you are having and without the support and understanding of your family members. Many of us share the same HCV symptoms, emotional and medical problems and the added burden of financial and insurance problems. HCV for many people is a very chronic progressive and debilitating illness sometimes fatal without a sure cure or treatment options that work successfully and long term for the majority of us. We also have many success stories to also share with you. Do you know your geno type or had a biopsy ??? Honey, I hope and pray natural remedies work for you and you have an easy time of it. Here we deal with our everyday HCV problems and issues in an open and honest discussion type format among friends. We deal with reality with truth and honesty about our HCV and lives and how it also effects all that know and love us. All The Best To You. Deb New Orleans HCV free liver transplant 3-4-01 failed responder to treatment meds again with chronic HCV Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 22, 2006 Report Share Posted March 22, 2006 Hi . Welcome. I’m sorry to hear you & your husband are suffering right now. I have prayed for compassion & understanding from his family. I’m a/k/a De a/k/a WWD. I’m a 48 y.o. single mom in GA, diagnosed in 2003, treatment thru 2004 & clear one year out at this point. Here’s a hug (((((())))))))))) De Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 14, 2006 Report Share Posted August 14, 2006 Welcome . You Joined A Great Family. Hope To Hear From You. D [pmcbride1@...] wrote: Hi , its me Pat..Ive been undetectable now 2 yrs & this group has helped me through treatment and then some..You will like it here...we have a host of wonderful loving and helpful people..If you need specific info, someone here will be glad to get it for you... Where are you from?...Im from san antonio Texas welcome and pop in and say hi.. Hugs, Pat -------------------------------------------------------------------------------- I am using the free version of SPAMfighter for private users. It has removed 320 spam emails to date. Paying users do not have this message in their emails. Try SPAMfighter for free now! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 14, 2006 Report Share Posted August 14, 2006 Hi, . Welcome to our family. I’m a/k/a De a/k/a WWD, outside Atlanta, GA & undetectable 1-1/2 years now. Pat is my tx (treatment) twin as we have the same damage, did tx together and the same results so far. We have people in all stages from newly diagnosed to never treated to post-transplant. We’re here for you. Introduce yourself when you feel like it and tell us a bit about you. De welcome Hi , its me Pat..Ive been undetectable now 2 yrs & this group has helped me through treatment and then some..You will like it here...we have a host of wonderful loving and helpful people..If you need specific info, someone here will be glad to get it for you... Where are you from?...Im from san antonio Texas welcome and pop in and say hi.. Hugs, Pat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 4, 2006 Report Share Posted September 4, 2006 Welcome Sally & Glenda! a/k/a De a/k/a WWD · New Files Visit Your Group Y! Messenger Quick file sharing Send up to 1GB of files in an IM. Photos Upload & Share Delight friends and family 360° Start Sharing Your place online Blog & photos .. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 22, 2006 Report Share Posted November 22, 2006 Yes, welcome Dr. McLaughlin, I've enclosed an example of what McLagan means when he says, "It is not about who is right or wrong, but rather, respecting each other and allowing others to express their opinions and thoughts in a professional manner. We shouldn't judge one another nor should we put each other down. We should be open to different thoughts, techniques and treatment." McLagan wrote: "I guess some are a bit slower than others; it's ok , soon you will get it. Please re-read slowly, then re-read again. Dr. Medlin understood and he seems like a smart guy, unfortunately you don't understand. I don't see how that is my problem. If you have any more intelligent questions, please ask again, but after you read my post one more time, even slower." Shad McLagan D.C. So be careful, that knife-like pain you feel in your back may not be a thoracic adjustment! (But, yes, welcome to the forum and enjoy!) (:-) M. s, D.C. Welcome Welcome Arah, it is good to see you on here. I think you would be a great moderator to this group. I am glad to see you are open and willing to discuss various topics with an open mind. It is not about who is right or wrong, but rather, respecting each other and allowing others to express their opinions and thoughts in a professional manner. We shouldn't judge one another nor should we put each other down. We should be open to different thoughts, techniques and treatment. We should be here to help one another and work together for the good of the patient.Shad McLagan D.C. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 22, 2006 Report Share Posted November 22, 2006 Thanks all of you for your welcome to the forum. My last email was, yes, to welcome all forms of thought and philosophies as I love to hear all ideas--- good or bad. My other intention was to subtly say " let's stop arguing" as it seems wasteful and so much more time can be spent towards lifting up our profession and each other. Yours in health and life, Arah McLaughlin, D.C. welcome Dr. McLaughlin:welcome to our little electronic camp fire!!!Agree we have to consider effective ways to make more people aware of the benefits of chiropractic care.Yours in health,Jack Pedersen DCSweet Home, Oregon Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 17, 2007 Report Share Posted January 17, 2007 WELCOME NEWBIE'S! GO LL BLESSINGS R Welcome Welcome to this great group Ladibug , i am sure you will love lifelift as much as the rest of us here do . Molly Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2007 Report Share Posted March 31, 2007 Sharon Honey Welcome to Group. Glad to see you again. love Dsuzie <suzieandsandy@...> wrote: Hello Blubird, Welcome to the family, What do you want us to call you? We have a loving little family here. I'm SuZie,a 56 year old female resident of the GWN (Great White North) a k a Thunder Bay, Ontario, Canada. We have some other Canadians here, also some Americans & I believe one Italian. The Group covers the spectrum. There are four or five of us Post transplant, a few on tx(treatment, some in SVR - Sustained Viral Response & some like me & Del who don't respond to tx & are now ESLD -End Stage Liver Disease & waiting for the go ahead for t p. I was dx'd in the early '90s but my docs & I believe I got it in the late "60s when I was heavily self-medicated. I was told I had "serum Hepatitis" which is now split into HBV & HCV. It was fun & I believe worth it. Now I live up here with my roommate SpYke - the Galactic Overlord in Training (aka a cat) He's almost got me trained now. You'll hear more of him later. Anyways, welcome to the family. If you have any questions, ask away. There is no such thing as a stupid question. If we don't have the answer, we'll find it somewhere. Check out the web site, there are some mini-bios of members there & a lot of files that may contain some of the answers you're looking. Welcome, SuZie & Sir SpYke the Fuzzy Next time I'm coming back as a cat Food fight? Enjoy some healthy debatein the Answers Food Drink Q&A. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2007 Report Share Posted March 31, 2007 WELCOME BLUBIRD, I AM PRETTY NEW HERE WELL ACTUALLY REAL NEW LOL. MY NAME IS PAT AND HAVE NEEN NICK-NAMED WW FOR WORRY WART LOL. THIS GROUP PEGGED ME RIGHT OFF THE BAT HAHA. I AM 1-B AND GOING ON TX WEDNESDAY EVENING. WENT ON GROUP CHAT FOR FIRST TIME AND HAD A BALL, IT WAS JUST TO COOL. I LIVE IN CALIFORNIA SOUTHERN PART AND I AM 61 AND BUBBA IS MY DRAGON LOL. SO GLAD YOU ARE HERE. HUGS TO YOU..WWsuzie <suzieandsandy@...> wrote: Hello Blubird, Welcome to the family, What do you want us to call you? We have a loving little family here. I'm SuZie,a 56 year old female resident of the GWN (Great White North) a k a Thunder Bay, Ontario, Canada. We have some other Canadians here, also some Americans & I believe one Italian. The Group covers the spectrum. There are four or five of us Post transplant, a few on tx(treatment, some in SVR - Sustained Viral Response & some like me & Del who don't respond to tx & are now ESLD -End Stage Liver Disease & waiting for the go ahead for t p. I was dx'd in the early '90s but my docs & I believe I got it in the late "60s when I was heavily self-medicated. I was told I had "serum Hepatitis" which is now split into HBV & HCV. It was fun & I believe worth it. Now I live up here with my roommate SpYke - the Galactic Overlord in Training (aka a cat) He's almost got me trained now. You'll hear more of him later. Anyways, welcome to the family. If you have any questions, ask away. There is no such thing as a stupid question. If we don't have the answer, we'll find it somewhere. Check out the web site, there are some mini-bios of members there & a lot of files that may contain some of the answers you're looking. Welcome, SuZie & Sir SpYke the Fuzzy Next time I'm coming back as a cat Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2007 Report Share Posted March 31, 2007 WW i do love the name. lol. Blubird is an awesome lady. love and hugs dpatricia <pandas2@...> wrote: WELCOME BLUBIRD, I AM PRETTY NEW HERE WELL ACTUALLY REAL NEW LOL. MY NAME IS PAT AND HAVE NEEN NICK-NAMED WW FOR WORRY WART LOL. THIS GROUP PEGGED ME RIGHT OFF THE BAT HAHA. I AM 1-B AND GOING ON TX WEDNESDAY EVENING. WENT ON GROUP CHAT FOR FIRST TIME AND HAD A BALL, IT WAS JUST TO COOL. I LIVE IN CALIFORNIA SOUTHERN PART AND I AM 61 AND BUBBA IS MY DRAGON LOL. SO GLAD YOU ARE HERE. HUGS TO YOU..WWsuzie <suzieandsandy > wrote: Hello Blubird, Welcome to the family, What do you want us to call you? We have a loving little family here. I'm SuZie,a 56 year old female resident of the GWN (Great White North) a k a Thunder Bay, Ontario, Canada. We have some other Canadians here, also some Americans & I believe one Italian. The Group covers the spectrum. There are four or five of us Post transplant, a few on tx(treatment, some in SVR - Sustained Viral Response & some like me & Del who don't respond to tx & are now ESLD -End Stage Liver Disease & waiting for the go ahead for t p. I was dx'd in the early '90s but my docs & I believe I got it in the late "60s when I was heavily self-medicated. I was told I had "serum Hepatitis" which is now split into HBV & HCV. It was fun & I believe worth it. Now I live up here with my roommate SpYke - the Galactic Overlord in Training (aka a cat) He's almost got me trained now. You'll hear more of him later. Anyways, welcome to the family. If you have any questions, ask away. There is no such thing as a stupid question. If we don't have the answer, we'll find it somewhere. Check out the web site, there are some mini-bios of members there & a lot of files that may contain some of the answers you're looking. Welcome, SuZie & Sir SpYke the Fuzzy Next time I'm coming back as a cat Food fight? Enjoy some healthy debatein the Answers Food Drink Q&A. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2007 Report Share Posted March 31, 2007 Hello, I am Sharon, 64, married and mother of 4 grown kids. I have HepC, have had for 30 years now;. I got it from a transfusion during an operation. I'm 2a, stage 2 fibrosis and grad 2 inflammation. I relapsed after tx back in 2000, but am in the 11th week of tx now with Roche drugs. Scherring last time. I'm not feeling too badly today, Sunday night is shot night, so I have another day to get caught up then Whammy!! again. lol I'm really not having a bad time this round, tho and am glad to meet you, hope to get to know many of you better, Sharon Welcome I am bursting with joy at all the new members we've been getting. I hope it means more people want education and support and not that more people are getting this nasty virus. Welcome to our crazy little family. I'm aka De. I'm 49, single mom in GA (almost empty nest), genotype 1, stage 1/grade 2, dx Halloween 2003, tx all thru 2004 and clear since week 12. I credit this group for my current level of sanity. It would have been WAY worse without them. Jump on in and introduce yourself as soon as you feel comfortable. You can learn a lot by reading, but we can't know how to support you if we don't know you. Do not ask God to guide your footsteps if you are not willing to move your feet! /De Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2007 Report Share Posted March 31, 2007 Sharon Thanks for joining us. I could not begin to tell you how great everyone here is. Big hugs to ya. love, Danne aka dSHARON CROSBY <csharonxoxo@...> wrote: Hello, I am Sharon, 64, married and mother of 4 grown kids. I have HepC, have had for 30 years now;. I got it from a transfusion during an operation. I'm 2a, stage 2 fibrosis and grad 2 inflammation. I relapsed after tx back in 2000, but am in the 11th week of tx now with Roche drugs. Scherring last time. I'm not feeling too badly today, Sunday night is shot night, so I have another day to get caught up then Whammy!! again. lol I'm really not having a bad time this round, tho and am glad to meet you, hope to get to know many of you better, Sharon . Food fight? Enjoy some healthy debatein the Answers Food Drink Q&A. Quote Link to comment Share on other sites More sharing options...
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