Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 Hi , I've been taking Viactiv a calcium supplement and has helped some, if you find a solution let me know. My DO used to give me B12 shots, but I haven't really needed to see him lately. Debbie Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 Hi Debbie, I do take lots of calcium. Maybe it isn't absorbing.I think the gp is afraid of the endo and giving me anything because the diabetes in finally under control again. Isn't this a backside of a disease? I hope I can get the results of the B12 next week. And here's a laugh, the gp requisitioned another TSH. It seems every time I turn around I am getting a TSH test for a doctor and they are always the same, low. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 e, Yes, they are the chewable candy like carmels. They have chocolate, carmel and cappuccino flavors. I like the chocolate best. My great aunt has been on synthroid for years, and has severe bone loss. When she went for a bone scan she gave me some pamphlets she picked up. When I read them it said that when a girl starts puberty they should start taking calcium. So, all three of us take them. Those chewable chalky things used to just gag me so calcium was the one thing I didn't take all the time. You take them after a meal. They have my great aunt on nose spray calcium, costs her almost $100.00 a month. I've read in medical books about GD patients being susceptible to get fibro- and myasthenia gravis has anyone else? Of course, my neighbor has fibro- and already thought I could be getting it. Yes, thank God for this group so we don't feel alone. We really need to find a doctor who has GD, they would understand. There is a picture of a doctor where I go and he looks like he has TED, I've wanted to call up and ask if he had GD, he is young. At least, all of us understand there is a real mystery to this disease and we can't all be crazy! LOL! Debbie ---------- > >To: <graves_supportegroups> >Subject: Re: Re: " Aches and Pains " and cramps too! >Date: Fri, Sep 15, 2000, 2:09 PM > > > Debbie, > > What is Viactiv? Is it those chewable candy thingys? > > e > > Re: Re: " Aches and Pains " and cramps too! > > >> >> Hi , I've been taking Viactiv a calcium supplement and has helped > some, >> if you find a solution let me know. My DO used to give me B12 shots, but > I >> haven't really needed to see him lately. >> >> Debbie >> >> ------------------------------------- >> The Graves' list is intended for informational purposes only and is not > intended to replace expert medical care. >> Please consult your doctor before changing or trying new treatments. >> ---------------------------------------- >> >> > > > ------------------------------------- > The Graves' list is intended for informational purposes only and is not > intended to replace expert medical care. > Please consult your doctor before changing or trying new treatments. > ---------------------------------------- > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 Hi Redhen, yes D and magnesium. I don't think it is a calcium problem. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 Hi Jody, that was just my gp. My endo want free T3 andT4. But it just goes to show that they do waste money. It is not the gooofy Graves people wanting these tests. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 Actually I think the rage thing is best thing about Graves. I seem to be settling down. I don't know if that's good. The rages used to keep my loved ones quite respectful. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 15, 2000 Report Share Posted September 15, 2000 Actually I think the rage thing is best thing about Graves. I seem to be settling down. I don't know if that's good. The rages used to keep my loved ones quite respectful. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2000 Report Share Posted September 16, 2000 Hi Debbie It is awful isn't it. I need to get more exercise - but I can't face walking further than absolutely have to. Well, I guess we all do our best. Cheers Caroline charles riley wrote: > > I had these symptoms, not being able to raise my arms above my head, just > felt like I had no strength left, I know I don't have the strength I used > too. That's why I thought I was going hyper again, but they took me off the > PTU said all my lab tests were in the normal range. Maybe this is just > another GD symptom mystery. My muscles in my arms (upper and lower) ache so > bad sometimes feels like it is in the bone. My legs same things. My > husband has notices the muscles in my upper legs seem awful tight, I can't > even bend the right one as much as the left one. > > Debbie > > ---------- > > > >To: " 'graves_supportegroups' " <graves_supportegroups> > >Subject: RE: Re: " Aches and Pains " and cramps too! > >Date: Fri, Sep 15, 2000, 9:37 AM > > > > > > > I'm printing this out and showing it to my doctor, coz that's *exactly* how > > I've been feeling lately. I could barely fold the towels out of the laundry > > yesterday! It literally hurt my upper arms, to lift the towels up. Hm. > > The doc hasn't called me with my lab results from 2 weeks ago. I suppose > > she would, if I had gone hypo. > > > > Kari > > > > Re: Re: " Aches and Pains " and cramps too! > > > > > > > > I never did experience any of this arm and hand numbness when I was hyper > > but since I have gone hypo (after RAI) I have been having all of the > > symptoms that have been mentioned dealing with my arms and hands: hands go > > numb while on the steering wheel, I wake up with my arms numb all of the > > time from sleeping, etc. It is also very hard for me to raise my arms to > > do stuff like washing and drying my hair, putting on makeup, etc. I never > > had any of these symptoms before going hypo. > > > > I was waking up every morning feeling like I had been run over by a truck > > (my back and shoulders were killing me). Since my doctor has upped my > > Synthroid I have experienced less muscle aches though. > > > > e > > > > e > > > > Re: Re: " Aches and Pains " and cramps too! > > > > > >> > >> Thanks, Viva. That bit of information did help. > >> > >> Does anyone else experience hand numbness on the steering wheel when > > driving? > >> > >> ------------------------------------- > >> The Graves' list is intended for informational purposes only and is not > > intended to replace expert medical care. > >> Please consult your doctor before changing or trying new treatments. > >> ---------------------------------------- > >> > >> > > > > > > ------------------------------------- > > The Graves' list is intended for informational purposes only and is not > > intended to replace expert medical care. > > Please consult your doctor before changing or trying new treatments. > > ---------------------------------------- > > > > ------------------------------------- > > The Graves' list is intended for informational purposes only and is not > > intended to replace expert medical care. > > Please consult your doctor before changing or trying new treatments. > > ---------------------------------------- > > > > ------------------------------------- > The Graves' list is intended for informational purposes only and is not intended to replace expert medical care. > Please consult your doctor before changing or trying new treatments. > ---------------------------------------- Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2000 Report Share Posted September 16, 2000 It is lupus, but it's not systemic and it resolves when you discontinue whatever drug caused it. Usually, but not always, the symptoms are limited to arthritis type stuff. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2000 Report Share Posted September 16, 2000 Hi , I only WISH the numbers would reflect how I feel, but they don't, and until they come up with some other way of testing something that is being missed, they won't...At least the FT3 gives a better idea of how I am converting T4. But my FT4 does not really indicate much in how I am feeling...in my opinion...unless of course I am STILL not understanding these darn tests...which is ALWAYS a possibility As for you being nervy...always be nervy , I love your posts, all of them Jody PS I know the TSH is an *indicator* that something is not right with the thyroid but it is a pituatary test...and it may take quite a while for it to catch up with what is going on in the whole endocrine system. ... Like I said, maybe I am still off base in my thinking here, and if I am, I hope someone will jump in...(hi Elaine ) _________________________________________________________________________ Get Your Private, Free E-mail from MSN Hotmail at http://www.hotmail.com. Share information about yourself, create your own public profile at http://profiles.msn.com. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 16, 2000 Report Share Posted September 16, 2000 Ummm Jody, I may be nervy saying this but don't you want your number to reflect how you feel, not someones' idea of how you should feel when your numbers fall within the normal range? Quote Link to comment Share on other sites More sharing options...
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