Guest guest Posted September 29, 2004 Report Share Posted September 29, 2004 Amie, You wrote: > I've stopped triathlon training due to my insomnia with the medication. ... I know > there have been > world class athletes who have been hypo - Smyers (thyroid cancer) and > Carl as well. Having run a couple of 10 km runs and stumbled through a marathon once in my misspent youth (long before I manifested hypoT), it is my considered opinion that triathletes are not members of the same species as those of us that are mere mortals. I cannot imagine a person with a normal thyroid doing these races, let alone someone on this list. So, about the best I can do is offer sympathy. You will need to make careful adjustments when you change activity levels. That means lots of tests and doctor's supervision. Don't change anything suddenly, if you can avoid it. Best of luck, Sedentary Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 29, 2004 Report Share Posted September 29, 2004 Thanks for the answers- makes sence now especially as I have been under physical pressure (aqua aerobic) and emotional pressures (youngest son just started uni) oh well will have to tamper with dosage to compensate. Any advice Chuck ???? Many thanks Lyn --- Sutherland <scorpiomks@...> wrote: > i feel that way quiet often,i am hypo plus have > constant sweating epesoides.anyone has this > probelm?Necie > Chuck B <cblatchl@...> wrote:evelyn tombs > wrote: > > > Can exercise make you feel really ill if you are > > hypoT? ... > > Absolutely. Exercise increases the rate at which you > use up T3. If you > are on T4 medication alone, this can even cause a > temporary onset of > symptoms when usage gets ahead of T4 to T3 > conversion. You also feel the > effects for several days while the T4 level > rebounds. > > I did this myself last Saturday when I helped move > some flagstone into a > garden for just two hours of heavy lifting. After > overdoing it, I had to > just sit for several hours, took a long nap, then > went to bed very > early, around 6:30 p.m.. I'm just starting to feel > normal again today. > > The problem is that we fine tune our dosage based on > the level of > exercise when we are sick, i.e. symptomatic of > hypoT, which is probably > not very active. Then, when we feel better, we try > to resume a healthy > active lifestyle and discover that our fine tuning > is no longer sufficient. > > We do best with a steady, predictable level of > exercise, and dosages > adjusted to that steady state. An excursion in > exercise level can really > be punishing. > > Chuck > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 29, 2004 Report Share Posted September 29, 2004 evelyn tombs wrote: > Thanks for the answers- makes sence now especially as > I have been under physical pressure (aqua aerobic) and > emotional pressures (youngest son just started uni) oh > well will have to tamper with dosage to compensate. > Any advice Chuck ???? If you do it yourself without testing, adjust in very small increments. Hyper-T can be fatal or at least seriously harmful. Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 29, 2004 Report Share Posted September 29, 2004 Thanks Chuck, Well in reality there are several reasons why I am not training. The primary reason at this point is fatigue. Both fatigue in the sense of the energy it takes to train, which I don't currently have, but also the fatigue brought on by the insomnia - I can't train for even two hours if I've only slept three. In my younger days, I would have said, 'oh well' and just trained anyway, but now that I've been diagnosed with many of these endocrinology problems, I'm trying to be more careful. Also, I'm getting physical therapy on my hip for a bike accident I was in this summer, so perhaps things work out this way for a reason in the end. This brings me to the 'other' reason I am not training right now. My doctor gave me some handouts and showed me a video before talking to me about the hypothyroid he found. Well, I saw that extreme dieting can bring this on, which I resorted to in the past - but it's kind of like the chicken and the egg there - who knows if being hypoT led me to have to extreme diet or if extreme dieting led to being more hypoT. So after diagnosis I slowed training and stopped dieting. I still want to lose now but am scared to diet at all, at least for now, so just try to maintain, although sometimes I get so hungry, I feel like I have to just eat and eat. Also, he mentioned that my extreme training could be whipping the hell out of my endocrine system. I previously told him that I over-trained when I started distance running several years ago, both in a sense that I trained too long and added distance too fast, and also that I didn't give myself enough recovery time. Well I am not so bad anymore, but still tended to overdo it - especially when work and school didn't allow enough rest for me to recover, I just said 'oh well' and kept on keepin' on. Recently, I joined another forum - 'workaholics anonymous' - so you can see my whole lifestyle leaned toward 'TYPE A'. I did some research and reading on hypoT and saw that a lot of it could be heredity as well, so I am not completely blaming myself anymore. I've taken up Hatha Yoga, and have been trying to lower my schedule to what most people would still consider somewhat 'busy' but for me is dramatically reduced. I still teach group exercise 5 days a week, weight train 2x a week and do yoga 2x a week, but the aerobics is a beginner class so for me the intensity is not high. I desperately want to return to triathlon and marathon training, but now I'm really scared to do it, because a part of me still blames myself for what is messed up. So yes, will need to return to it slowly and gradually - that is definitely not my style but will do what I can. At any rate, I will not return to full on training until things have leveled off with my energy levels - to where I don't feel so dead, I have ample energy to deal with my daily activities, and when I get up I feel energized rather than dragging myself out of bed. Right now that seems like a dream - occasionally I get glimpses of this but not more - and I don't know when that day will come but hopefully, soon. Thanks!! -Amie Re: New on Board Amie, You wrote: > I've stopped triathlon training due to my insomnia with the medication. .... I know > there have been > world class athletes who have been hypo - Smyers (thyroid cancer) and > Carl as well. Having run a couple of 10 km runs and stumbled through a marathon once in my misspent youth (long before I manifested hypoT), it is my considered opinion that triathletes are not members of the same species as those of us that are mere mortals. I cannot imagine a person with a normal thyroid doing these races, let alone someone on this list. So, about the best I can do is offer sympathy. You will need to make careful adjustments when you change activity levels. That means lots of tests and doctor's supervision. Don't change anything suddenly, if you can avoid it. Best of luck, Sedentary Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2004 Report Share Posted September 30, 2004 LOL Thank God I am not doing lots of tests and doctor supervision! I couldn't stand it. Gracia > So, about the best I can do is offer sympathy. You will need to make > careful adjustments when you change activity levels. That means lots of > tests and doctor's supervision. Don't change anything suddenly, if you > can avoid it. > > Best of luck, > Sedentary Chuck > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2004 Report Share Posted September 30, 2004 evelyn tombs wrote: > Thanks for the advice Chuck-maybe I'd be best staying > on the 100mcg the doc put me on?? I'm not doing that > aqua aerobics this week as I hurt too much all over > and am too tired-thought maybe I need to rest a bit, > what do you think? Rest is good. Pain is an indicator. If the 100 mcg is T4, you will probably need another increase before too long. If you can, you should maintain your most likely or minimum exercise level for at least a weak before the next test. That way your dosage will be tuned to that level rather than a resting one. Chuck Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2004 Report Share Posted September 30, 2004 yes T3 " pushes " adrenals and exposes adrenal insufficiency. Gracia > Well didn't start feeling tired but wired until the Cytomel came into play, > and I was taking the dosage too late at night and not sleeping. Things have > been leveled out now as far as that goes, but I'm still more tired than > anything else, so think the dosages still need to be adjusted there. > > > > -Amie > > > > > > _____ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2004 Report Share Posted September 30, 2004 exercise intolerance is linked to low T3 levels. Gracia > > Can exercise make you feel really ill if you are > hypoT? I had started to feel wonderful, just like the > old me, then I took up aqua aerobics. Now I ache from > head to foot, lymph nodes are up in my neck, having > trouble eating because I feel sick and I just feel > like I am burned out??? > > Any ideas about this would be greatly appreciated > > Thanks guys > > Lyn > > > > > --- Amie <amie1@...> wrote: > > > No, I totally understand. I've been a competitive > > triathlete and marathoner > > and was stricter about my diet than anyone I knew, > > and it would take forever > > to lose any weight or I would just gain. And if I > > pigged out even one meal, > > forget it, all the weight would come back. I was > > swimming 3000 meters a > > week, running 30-45 miles per week, and cycling 100+ > > miles per week and was > > not losing, eating 1500-1800 calories a day. Go > > figure. > > > > > > > > I am still not losing but just started Cytomel about > > a month ago. My > > appetite goes up so much sometimes, but I guess that > > is part of the > > adjustment phase. I feel wired or tired, depending > > on the dose change and > > resulting insomnia. > > > > > > > > Are you starting medication or what? > > > > > > > > -Amie > > > > > > > > _____ > > > > From: Sue Walloch [mailto:smkatz3.1@...] > > Sent: Tuesday, September 28, 2004 1:04 PM > > hypothyroidism > > Subject: New on Board > > > > > > > > Hi! > > I'm Sue from Lakewood, CO. I found out I was > > hypothyroid in March > > 22, 2004. I went to see the dr about depression (I > > hadn't been to > > the dr for years), and he immediatly ran a blood > > test for my > > thyroid. I feel very fortunate after reading so > > much on how > > difficult it can be to get diagnosed. > > I'm 42 and I started experiencing problems with > > losing weight, I just > > thought it was about hitting the big 4-0. I've > > exercised regularly > > since I was 28. I was getting extremely frustrated > > wondering how > > much I had to exercise and how little I had to eat, > > now that I'm in > > my 40's. It's still frustrating: It takes 2 weeks > > to lose 2 pounds > > and then I gain those 2 pounds back overnight. > > Sue from CO > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted September 30, 2004 Report Share Posted September 30, 2004 I think I figured out what is going on with my Cytomel, possibly. Before when I took it at 9 am and 9 pm, I was in a situation to where I could not eat for about two hours afterwards, and in the pm, usually didn't eat at all afterwards - when I had the sleep problems. So I didn't eat two hours before and at least two hours after. When I went to 6 am and 6 pm, I have been eating exactly one hour afterwards both times. So I think the absorption is reduced now that that time interval has shortened. I am going to try the next few times waiting two hours after I take the pill and see if it makes a difference. I spoke with my doctor's office today and they didn't advise one way or another, said everyone is different and you have to go with what works for you. -Amie .. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 11, 2005 Report Share Posted August 11, 2005 Hi , Welcome to . You've picked a fine place to come and learn about cochlear implants. It's very normal to be worried and scared of surgery of any type and I think one of the most important things one can know from the start is that it is in no way brain surgery as some folks have thought at first. We have over 950 members on this forum. All are in some way involved with cochlear implants.. Either having the implant themselves or having a family member or friend with an implant or just exploring their options as you are. Being one of 4 family members who have implants, I can tell you, the minimal risks have been well worth what our family has gained in the hearing world.. independence, a new lease on life, one filled with a clarity of sound that we never thought would happen again in our lifetime. We have bilateral progressive nerve deafness which began for the most part in our late teens, early twenties and progressed from mild to profound over the years. So many improvements have been made in recent years and I would encourage you to stick around here, ask questions and put your fears and concerns to rest for the most part. Please feel free to email me privately or here on the forum and I'd be happy to talk with you. Once again, welcome.. Hope you enjoy your stay with us and find lots of helpful information. A good place to start would be to browse our website.. www..com there you will find many stories, tips for getting through the ci process and much more. Please let us know how we can help. Warm regards, Silly MI In , " nnjl97 " <nnjl97@y...> wrote: > I HAVE RECENTLY BEEN TOLD I QUALIFY FOR A COCHLEAR IMPLANT. I WILL > BEGIN ALL THE APPOINMENTS THE END OF AUGUST. YES I AM SCARED AND > NERVOUS ABOUT HAVING THIS DONE. I HAVE NOT MADE MY MIND UP IF I WILL > AGREE TO IT. SO WITH THAT I WOULD APPRECIATE ANY AND ALL HELP TO LET > ME KNOW EVERYTHING THAT I CAN ABOUT THIS. I AM 50 AND HAVE BEEN NOT > HEARING MUCH FOR A LONG TIME. PLEASE ANY HELP YOU CAN GIVE WOULD BE SO > GREATFUL > THANK YOU > LINDA > YOU CAN ALSO SEND MAIL TO MY AOL ACCT. > NNJL97@A... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 > Hi linda > welcome to CI Hear.I am glad that you are a candidate for a CI and I certainly hope that after hearing what so many will be telling you about how their implants changed their lives and that of their loved ones you will be ready by the end of August to begin your own journey! I will be celebrating my 9th anniversary on Aug 26.I was profoundly deaf for 10 years before i heard about the CI ..Now I am having the time of my life with my family and friends and oh,yes I bond rapidly with strangers too!It is so nice just to be back in the hearing world. > > When you have your appts you will be shown the implant and processors..your Dr and audiologist will tell you all about them and you will be able to ask any questions that you wish.Of course,like you are already doing,you can ask questions here and you will receive alot of answers and support > > I wish you the best > Dora Weber > > dora_weber@m... > > Bilateral > N22-96 > N24C-01 > Cochlear Otosclerosis > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted August 12, 2005 Report Share Posted August 12, 2005 , Welcome aboard. After you have a chance to read and ask questions on here I bet a lot of your fears will be reduced. I am not afraid of much so I spent a lot of my time learning all about the CI's and I asked a LOT of questions. After having my CI for over a year I still don't have all the answers but please ask any questions you have on here and someone should be able to get you an answer. You can read my story here: http://www..com/Images/EvelsStoryPartOne.jpg http://www..com/Images/EvelsStoryPartTwo.jpg Cheers, Evel Nucleus Advocate N24c 05/05/04 > I HAVE RECENTLY BEEN TOLD I QUALIFY FOR A COCHLEAR IMPLANT. I WILL > BEGIN ALL THE APPOINMENTS THE END OF AUGUST. YES I AM SCARED AND > NERVOUS ABOUT HAVING THIS DONE. I HAVE NOT MADE MY MIND UP IF I WILL > AGREE TO IT. SO WITH THAT I WOULD APPRECIATE ANY AND ALL HELP TO LET > ME KNOW EVERYTHING THAT I CAN ABOUT THIS. I AM 50 AND HAVE BEEN NOT > HEARING MUCH FOR A LONG TIME. PLEASE ANY HELP YOU CAN GIVE WOULD BE SO > GREATFUL > THANK YOU > LINDA > YOU CAN ALSO SEND MAIL TO MY AOL ACCT. > NNJL97@A... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted November 21, 2007 Report Share Posted November 21, 2007 > > Dear Group, > > Abundant blessings to all of you. I apologize for being slow to get to my ! mail. I hope I can keep up with you guys. I want to post a prayer and writing from time to time, if this is ok. I'm so excited to be a part of this. You all seem like great people. > Peace, love and light > Laney > > > --------------------------------- > Get easy, one-click access to your favorites. Make your homepage. > Hello Laney, Welcome aboard. Blessings to you also. I just wanted to say that this is the most wonderful group I have ever been a part of. It does sometimes get overwelming with the mail intake, but I love it. It makes my day great. There is nothing better than to get online and see how many people in the world feel the same as I do. I have been so long looking for others like this. There have been times when I thought how I wish others could love and feel the same way I do. My spirit guide has led me to this group and for that I am most thankful. I feel on top of the world since I joined this group just a few days ago. It is the best thing that ever happened to me. It made me see that I am not alone and it gives me the strength to endure anything that comes my way. This group is a godsend. So to everyone who is a part of HH, bless you all and know that my heart goes out to each and everyone of you, my brothers and sisters. Thanks for making a difference in my life and so many others. Bless you all. Quote Link to comment Share on other sites More sharing options...
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