Guest guest Posted July 1, 2004 Report Share Posted July 1, 2004 , I also had the thought while reading your post that many people only wish their greatest concern about vacation was the decision of whether to rent a house or a condo. Sounds as though you husband is a lucky man to have you. I think one of the other that responded to you may be right about men and their reactions to things they can't control. Your being the major bread winner and ill at the same time is probably an emotional and psychological overload for you husband. I am sure that if you can make him see this illness as a real thing he will come around to realizing that you need his help. But that is all a side note really. The main reason I am writing you is to suggest that you have your thyroid check. Shortness of breath is actually a symptom of thyroid problems. And there is a type of autoimmune thyroid disease that could be reacting to your PA or visa versa. Pamela Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2004 Report Share Posted July 1, 2004 Dear Fran, I have learned from the best...YOU!!! I have shared those tips with so many people and they seem to impact everyone I know that reads them. Belated birthday wishes, and may I say, I am delighted you had some quality time with your girls!! be well Fran... love annie and the pugherd Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2004 Report Share Posted July 1, 2004 In a message dated 7/1/2004 5:48:39 AM Eastern Standard Time, heatherfitz@... writes: Finally, I started with my first injections of Enbrel yesterday...keep you fingers crossed! , by the way, love the name. It is my daughter's name. Good luck with the enbrel. Most people are very happy with it. I am taking Humira and it is helping somewhat. You sound like you have great job. What type of work do you do? Hopefully your husband will come around. I used to forward my husband some postings for this board that I thought would help him make things sink in more. Janet Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2004 Report Share Posted July 2, 2004 Dear Annie, Thank you for the kind words. I wish I could take credit for the chronic pain tips, but I only found them one night on the Internet and there was no author listed. I'm glad they have helped you and when I re read them I'm always amazed at how many of them relate to me that day. Thanks for the birthday wishes and it was a great day for me. I'm trying my best to get well and it helps finding the courage to go on from all of you in this group. Love, Fran Re: [ ] need some advice Dear Fran, I have learned from the best...YOU!!! I have shared those tips with so many people and they seem to impact everyone I know that reads them. Belated birthday wishes, and may I say, I am delighted you had some quality time with your girls!! be well Fran... love annie and the pugherd [ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2004 Report Share Posted July 2, 2004 It's ironic actually...I work in pharmacutical research (Market not lab). I rarely tell the physicians this since I have found that they then either think I am trying to second guess them or talk way over my head. Unfortunatly, I also get to hear first hand what the docs think of various drugs - sometimes things they would never tell us as a patient. > > In a message dated 7/1/2004 5:48:39 AM Eastern Standard Time, > heatherfitz@r... writes: > > Finally, I started with my first injections of Enbrel > yesterday...keep you fingers crossed! > > > > , > > by the way, love the name. It is my daughter's name. Good luck with the > enbrel. Most people are very happy with it. I am taking Humira and it is > helping somewhat. You sound like you have great job. What type of work do you > do? Hopefully your husband will come around. I used to forward my husband > some postings for this board that I thought would help him make things sink > in more. > Janet > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2004 Report Share Posted August 1, 2004 I am not sure if it is always the case but in Spanish soy is soya. > My 6 year old daughter has been on ZP, AFP & NF for 5 weeks now, > apart from her being a little hyper during the day (I give her epsom > salts in a cream for this) I have not seen any improvement in her > behaviour. I wonder if I am doing something wrong, or the enzymes > are not the correct ones for her. I give her mostly the ZP & NF > because she is a big organic rice milk drinker. She hardly eats but > what she does, I have it covered with the ZP, AFP & NF. I give her > one capsule each of ZP & NF with her organic rice milk (on your > advice). When she does eat food I give her just capsule of each. > > My daughter had the PICA test done and was found to have high lead > and low iron. I give her SNT, Zinc, Vit's C & E, Calcium, Bio Kult > (Probiotic) & Eye-Q (fish oil)and TMG. I also rub Epsom Salts on > her 3-4 x per day. Her night sleeping has improved (she often woke > up several times during the night, or woke up at 3am and stayed away > for the rest of the night). Unfortunately she is still eating non- > food items (she especially likes the cement between bricks!!). > > I can honestly say, that behaviour wise she has not changed - except > she appears more hyper during the day light hours. She isn't > talking anymore then she used to, and she is still head banging. > She hasn't had any bad reactions to the enzymes though, (no stomach > pains or terrible poop). As far as i know she has never suffered > with yeast/bacteria, never really been on antibiotics (just > occasionally maybe once a year if that). No ear infections. In > fact she is pretty much in good health considering she hardly eats, > and gets alot of non-food items in her system. > > Finally, I have just started to use non-fluoride toothpaste (started > 2 days ago) and I have started to give her filtered water (again 2 > days ago). She isn't on the gf/cf diet or any other diet because > she hardly eats (smells everything, before it even goes into her > mouth......if it ever gets into her mouth!!!). > > Can you tell me also, is soy the same as soya? (We don't use this > product, but have noticed it alot and wondered if soy is also known > as soya). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 1, 2004 Report Share Posted August 1, 2004 > My 6 year old daughter has been on ZP, AFP & NF for 5 weeks now, > apart from her being a little hyper during the day (I give her epsom > salts in a cream for this) I have not seen any improvement in her > behaviour. For my son, the enzymes did not address all foods. You might have that same problem with your child. > because she is a big organic rice milk drinker. My son did not tolerate rice, even with enzymes. Try removing it [yes I know, probably not an easy thing to do]. > My daughter had the PICA test done and was found to have high lead > and low iron. I give her SNT, Zinc, Vit's C & E, Calcium, Bio Kult > (Probiotic) & Eye-Q (fish oil)and TMG. SNT is notorious for causing eating problems. Try removing it, or at least reducing it to about 1/4 what you are currently giving her. >>Unfortunately she is still eating non- > food items (she especially likes the cement between bricks!!). This can be zinc deficiency, but for my #3, it meant he was eating a food or supplement he did not tolerate, or he had a yeast issue. > I can honestly say, that behaviour wise she has not changed - except > she appears more hyper during the day light hours. Rice made my son very hyper and stimmy, even with enzymes. My son did not tolerate artificials, rice, corn, and luteins, even with enzymes. Good luck. Dana Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 11, 2004 Report Share Posted October 11, 2004 Dear Annie, Well I have the guttate form of psoriasis, at least my rheumatologist says I do. (I've seen two dermatologists who have told me it is a rare form of skin damage. Personally, I believe my arthritis doctor since I have every other sign of it pointing to PA. Anyway, normally my spots are about the size of a cigarette burn. Some are smaller and very few are larger. I have had them fill with fluid only once, thank goodness. They didn't change color, but did get really red...since they are normally red I didn't think that was a big deal. They would itch and hurt at the same time and when they did drain it normally was a clear fluid. It drove me nuts and like I said has only happened one time. If yours doesn't go away or continues to drain, I would go to the doctor and get it checked out. I was really ready to go with my situation and it basically just seemed to clear up on it's own. With all the stories of skin cancer, it's really important to rule everything out. I'm sure it's only bad PA, but this way you don't or won't have to worry. Well I'd say, I know what you are going through, but every one is different. So I won't Just go to the doctor, the dermatologist just love to hear about rashes and things like that...lol. Take care and I hope you are feeling better. Love, Fran [ ] need some advice Hello, usually a lurker here, but I have a question..kind of an indelicate one!! sorry in advance! I have basic plaque P on my knees and elbows and a little on my back, and scalp, but I also have the kind that comes up as a bump on my skin with a little head to it...not sure if that makes it Guttate or Pustular. Anyway, got a couple of these all in the same area. It was sooooooo sore! I am used to the first eruption day being sore, then the the " head " breaks open, relieves the pressure and all it goes away in a few days. HOWEVER, this time I have had a bit more of an issue. Apparantly there were 3-4 of these in one area. The small lumps looked like they were turning black and blue under my skin. Finally I put a hot wash rag on the area, needless to say, the draining began. I will NOT describe it!!! Has anybody ever had anything like this??? I feel like I am turning into a freak of nature. Any advice would be most appreciated. thanks annie and the pugherd Quote Link to comment Share on other sites More sharing options...
Guest guest Posted October 11, 2004 Report Share Posted October 11, 2004 Dear Annie, Not sure if this helps and I've refrained from writing because I'm not sure it's the same ~ and I don't recall much of the technical stuff, but it sounds soooo similar... My daughter (a few years back) suffered from something very similar. It started in her armpits and by the time we finally figured out what to do, it was all down her sides and on her arms and legs. It would get better in the winter (very dry here) and much worse in the summer. She had bumps that almost looked like pimples, but the liquid was clear and she would often get a red circle around the bumps the size of a quarter or bigger sometimes ~ and it semed they would mutliply in a certain area. Anyway, the diagnosis finally was a form of infected acne, but this form isn't the same as what is on the face, but they used the same medicine I had for acne (I'm one of those lucky 41 year olds that still get cystic acne now and then ~ especailly now ~ seems tied either to the med's or the PA), anyway, it cleared it up within a week or so! Good Luck.... From: pugbunch13 [mailto:annie@...] Sent: Monday, October 11, 2004 2:55 PM Subject: [ ] need some advice Hello, usually a lurker here, but I have a question..kind of an indelicate one!! sorry in advance! I have basic plaque P on my knees and elbows and a little on my back, and scalp, but I also have the kind that comes up as a bump on my skin with a little head to it...not sure if that makes it Guttate or Pustular. Anyway, got a couple of these all in the same area. It was sooooooo sore! I am used to the first eruption day being sore, then the the " head " breaks open, relieves the pressure and all it goes away in a few days. HOWEVER, this time I have had a bit more of an issue. Apparantly there were 3-4 of these in one area. The small lumps looked like they were turning black and blue under my skin. Finally I put a hot wash rag on the area, needless to say, the draining began. I will NOT describe it!!! Has anybody ever had anything like this??? I feel like I am turning into a freak of nature. Any advice would be most appreciated. thanks annie and the pugherd Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2004 Report Share Posted November 6, 2004 April try some hot apple cider, its great on these cold mornings...then try cranberry juice heated with a cimmon sticks... Use your imagineation..... Hugs Cary Sue Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2004 Report Share Posted November 6, 2004 Hi April, Dave here. Just wanted to let you know that once I started taking my Whey protein, it really helped to curb cravings. If you have already started the Whey then we will mark it up as, we are going to have a craving every now and then. Good luck God Bless, Dave (636) 240 - 0663 MGB 03-04-03, Dr H. Changing the world one soul at a time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2004 Report Share Posted November 6, 2004 I drink Soyfee some times - it's a good coffe alternative - you can order it on line or some health food stores carry it. It's great for you and tastes like coffee - it's pretty good - I drink it with low carb hazelnut creamer - yummy!!!! They also had a tanic free tea at the MGB meet and greet in NC before the picnic- I'm not sure what it's called but would like to know - I really could go for some tea right now and if it's safe for us - I'd like to taste it. If anyone knows what I'm talking about - please let me know - my local health food store would like to order some if I just had the name and compnay that makes it. Hope this helps! Michele S () 8/3/04 390/323/??? Dr. H & Raj. in FL Don't forget to RSVP for the MidWest MGB Holiday Party in Jefferson City, MO!!! e-me if interested! chels_70@... :-) April <thegreatwolves@...> wrote: Hey guys. I was just wondering what I can have for a drink. It's been 4 months and I haven't had coffee and I don't crave it either. But lately I have been wanting a hot drink and I don't like hot chocolate and I now we are not to have tea or coffee so I was wondering what else there was. Any advice would be appreciated. Thanks. April Ontario Canada 06-30-04 (=';'=) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2004 Report Share Posted November 6, 2004 Hi, I have a cup of hot chicken broth every morning when everyone else at the office is having coffee. I actually look forward to it each morning. I am having a hot drink and also getting some of the sodium for the day. Try it--I think you'll like it. I also found some " acid tamer " that I use for the occasional cup of coffee that I have. Good Luck, S. need some advice > > > Hey guys. I was just wondering what I can have for a drink. It's > been 4 months and I haven't had coffee and I don't crave it either. > But lately I have been wanting a hot drink and I don't like hot > chocolate and I now we are not to have tea or coffee so I was > wondering what else there was. Any advice would be appreciated. > Thanks. > > April Ontario Canada > 06-30-04 > (=';'=) > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2004 Report Share Posted November 6, 2004 My only craving is for a hot drink i was trying to figure out what i could have that was hot besides chocolate becasue i dont like the hot chocolate. I dont miss the coffee or pop. i just miss something hot. lol I am taking my whey protein already ahve been for months now. April Ontario Canada. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 6, 2004 Report Share Posted November 6, 2004 thanks i will look for that next time in town. i appreciate it. April Ontario Canada Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2004 Report Share Posted November 7, 2004 Hot apple cider, apple juice with spices. Monroe MGB 7/19/2002..Dr. Rutledge 285/125 CLOS-High Point 704-682-0260 (cell) 336-841-0326 (office) npm@... www.clos.net need some advice Hey guys. I was just wondering what I can have for a drink. It's been 4 months and I haven't had coffee and I don't crave it either. But lately I have been wanting a hot drink and I don't like hot chocolate and I now we are not to have tea or coffee so I was wondering what else there was. Any advice would be appreciated. Thanks. April Ontario Canada 06-30-04 (=';'=) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 7, 2004 Report Share Posted November 7, 2004 A combination of orange juice, pineapple juice and cranberry juice with cinnamon sticks is also good hot. Monroe MGB 7/19/2002..Dr. Rutledge 285/125 CLOS-High Point 704-682-0260 (cell) 336-841-0326 (office) npm@... www.clos.net Re: Re: need some advice My only craving is for a hot drink i was trying to figure out what i could have that was hot besides chocolate becasue i dont like the hot chocolate. I dont miss the coffee or pop. i just miss something hot. lol I am taking my whey protein already ahve been for months now. April Ontario Canada. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2004 Report Share Posted November 8, 2004 Was just wondering what the 240 - 0663 means? Sorry to be feeling kind of dumb here? Thanks... since your surgery was around the same time as mine I find it interesting... thanks for your reply, Barb/ n/e oHIo -107 lbs., thank you God! Dr. R (the best) >>> <iwitness4u@...> 11/06/04 08:32PM >>> Hi April, Dave here. Just wanted to let you know that once I started taking my Whey protein, it really helped to curb cravings. If you have already started the Whey then we will mark it up as, we are going to have a craving every now and then. Good luck God Bless, Dave (636) 240 - 0663 MGB 03-04-03, Dr H. Changing the world one soul at a time. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2004 Report Share Posted November 8, 2004 That's Dave's phone number. Re: need some advice > > Was just wondering what the 240 - 0663 means? > Sorry to be feeling kind of dumb here? > Thanks... since your surgery was around the same time as mine I find it > interesting... > > thanks for your reply, > Barb/ n/e oHIo -107 lbs., thank you God! > Dr. R (the best) > >>>> <iwitness4u@...> 11/06/04 08:32PM >>> > > Hi April, Dave here. Just wanted to let you know that once I started > taking > my Whey protein, it really helped to curb cravings. If you have already > started the Whey then we will mark it up as, we are going to have a > craving every > now and then. Good luck > > God Bless, > Dave (636) 240 - 0663 > MGB 03-04-03, Dr H. > > Changing the world > one soul at a time. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2004 Report Share Posted November 8, 2004 isn't that his phone number? cathy s > Was just wondering what the 240 - 0663 means? > Sorry to be feeling kind of dumb here? > Thanks... since your surgery was around the same time as mine I find it interesting... > > thanks for your reply, > Barb/ n/e oHIo -107 lbs., thank you God! > Dr. R (the best) > > >>> <iwitness4u@a...> 11/06/04 08:32PM >>> > > Hi April, Dave here. Just wanted to let you know that once I started taking > my Whey protein, it really helped to curb cravings. If you have already > started the Whey then we will mark it up as, we are going to have a craving every > now and then. Good luck > > God Bless, > Dave (636) 240 - 0663 > MGB 03-04-03, Dr H. > > Changing the world > one soul at a time. > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 8, 2004 Report Share Posted November 8, 2004 Hot apple cider is yummy on a cold winter night!! And you can have all you can stand ;-) Kellie in OKC 12-19-03 >From: " April " <thegreatwolves@...> >Reply- > >Subject: need some advice >Date: Sun, 07 Nov 2004 00:36:56 -0000 > > >Hey guys. I was just wondering what I can have for a drink. It's >been 4 months and I haven't had coffee and I don't crave it either. >But lately I have been wanting a hot drink and I don't like hot >chocolate and I now we are not to have tea or coffee so I was >wondering what else there was. Any advice would be appreciated. >Thanks. > >April Ontario Canada >06-30-04 >(=';'=) > > > _________________________________________________________________ Is your PC infected? Get a FREE online computer virus scan from McAfee® Security. http://clinic.mcafee.com/clinic/ibuy/campaign.asp?cid=3963 Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2005 Report Share Posted March 12, 2005 Welcome , I'm sorry about your dx, but glad you have found the right place to be for support. What type of meds has your doctor put you on? It is hard for the family to take all this in, some have no clue what RA is. With your Mom knowing what it is, and how it affected her Dad I can see how devastating it will be for her. I can't really give any advice, because I don't know her, know what I mean? But, maybe she could go with you to your rheumy, and let him talk to her about all the new meds, and what your options are. We mother's always worry about our children you can't stop that. It might take awhile for her to understand it all, but it will be great that she is right by your side in what you go through. Good luck, and let us know how it goes, will be thinking of you, Tawny --- In , " dianaenxing " <dianaenxing@y...> wrote: > > > Okay, so I've been officially diagnosed for almost 2 weeks now and > still cannot figure out how to tell my parents. I think my dad will > be okay with it once I tell him how optimistic my rheumatologist has > been. My mom, on the other hand, has always been a worrier. Her dad > had RA like 25 years ago when the medicines and other advances in > the disease had not been made. He passed away 20 years ago and all > she can remember were the gold shots he received and how he had to > wear slippers all the time because of his foot pain. My doctor says > that it will not be like that for me. I guess my question for which > I'm seeking advice is---how do I tell her so that it doesn't come > off sounding like a horrible thing? She's going to think the worst > right away by just hearing the word 'rheumatoid.' I mean, this was > the same woman who cried when they told me I didn't have RA a year > ago. (of course, now we know the disease hadn't taken shape then) I > just need a way to tell her gently and to let her know that I'm > going to be all right. Any advice on talking to family would be a > HUGE help! Thanks, everyone. > > E. > New Orleans, LA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2005 Report Share Posted March 12, 2005 Welcome , I'm sorry about your dx, but glad you have found the right place to be for support. What type of meds has your doctor put you on? It is hard for the family to take all this in, some have no clue what RA is. With your Mom knowing what it is, and how it affected her Dad I can see how devastating it will be for her. I can't really give any advice, because I don't know her, know what I mean? But, maybe she could go with you to your rheumy, and let him talk to her about all the new meds, and what your options are. We mother's always worry about our children you can't stop that. It might take awhile for her to understand it all, but it will be great that she is right by your side in what you go through. Good luck, and let us know how it goes, will be thinking of you, Tawny > > > Okay, so I've been officially diagnosed for almost 2 weeks now and > still cannot figure out how to tell my parents. I think my dad will > be okay with it once I tell him how optimistic my rheumatologist has > been. My mom, on the other hand, has always been a worrier. Her dad > had RA like 25 years ago when the medicines and other advances in > the disease had not been made. He passed away 20 years ago and all > she can remember were the gold shots he received and how he had to > wear slippers all the time because of his foot pain. My doctor says > that it will not be like that for me. I guess my question for which > I'm seeking advice is---how do I tell her so that it doesn't come > off sounding like a horrible thing? She's going to think the worst > right away by just hearing the word 'rheumatoid.' I mean, this was > the same woman who cried when they told me I didn't have RA a year > ago. (of course, now we know the disease hadn't taken shape then) I > just need a way to tell her gently and to let her know that I'm > going to be all right. Any advice on talking to family would be a > HUGE help! Thanks, everyone. > > E. > New Orleans, LA Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2005 Report Share Posted March 12, 2005 , this will be a hard thing to do, I'm sure. All I know to do is just explain to her that things have changed since her dad had RA. New medications can prevent the damage to the joints that he probably had. But this is a two-edged sword. At least you have someone who will understand what you are going through with RA. Many people have no one with empathy for them. " But you don't look sick " is often heard. You will be able to talk to your mother about your RA, and she won't have that attitude. Sue On Friday, March 11, 2005, at 10:19 PM, dianaenxing wrote: > > Okay, so I've been officially diagnosed for almost 2 weeks now and > still cannot figure out how to tell my parents. I think my dad will > be okay with it once I tell him how optimistic my rheumatologist has > been. My mom, on the other hand, has always been a worrier. Her dad > had RA like 25 years ago when the medicines and other advances in > the disease had not been made. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 12, 2005 Report Share Posted March 12, 2005 , this will be a hard thing to do, I'm sure. All I know to do is just explain to her that things have changed since her dad had RA. New medications can prevent the damage to the joints that he probably had. But this is a two-edged sword. At least you have someone who will understand what you are going through with RA. Many people have no one with empathy for them. " But you don't look sick " is often heard. You will be able to talk to your mother about your RA, and she won't have that attitude. Sue On Friday, March 11, 2005, at 10:19 PM, dianaenxing wrote: > > Okay, so I've been officially diagnosed for almost 2 weeks now and > still cannot figure out how to tell my parents. I think my dad will > be okay with it once I tell him how optimistic my rheumatologist has > been. My mom, on the other hand, has always been a worrier. Her dad > had RA like 25 years ago when the medicines and other advances in > the disease had not been made. Quote Link to comment Share on other sites More sharing options...
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