Guest guest Posted April 17, 2006 Report Share Posted April 17, 2006 Hi , yes, for the longest time, the weather has also affected me too. Hot/humid to cold/humid cause pain flareups quite often. I feel like a human barometer. Rhonda weather and pain hi! does the change in weather esp. damp/humid and/or rain bring on more intense body pain and mental fog to ya's? It does to me. The Neurologists I see will not prescribe any kind of pain meds.,I'm to take ib's or tylanol, do yoga and aqua therapy and of course desent diet. Does anyone else have celliac (spg) disease too? Thanks Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2006 Report Share Posted April 17, 2006 Hi, I'm new here-- just been lurking for a few days. I'm from central Illinois where we have had rain, wind, tornados, damp, cold, weather for a few weeks (seems like forever). My arthritis is killing me!! My hands are so sore I can hardly use them. Been taking Aleeve, but it doesn't seem to touch it in this weather. I have Vicodin which helps the most, but don't want to get to cozy with it!! I just need some DRY, WARM, sunshine!! Mitzi RE: weather and pain Hi , yes, for the longest time, the weather has also affected me too. Hot/humid to cold/humid cause pain flareups quite often. I feel like a human barometer. Rhonda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2006 Report Share Posted April 17, 2006 HI Ladies and Gents... Yes, weather does effect me. Especially when the pressure goes down. I have been in horrable pain the last 3 days and each day that I think it can't get worse it does. Nothing seems to work, meds, relaxers, or bio-feedbk. It could be spring but I really don't know any more... Rhonda Huffman wrote: Hi , yes, for the longest time, the weather has also affected me too. Hot/humid to cold/humid cause pain flareups quite often. I feel like a human barometer. Rhonda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2006 Report Share Posted April 17, 2006 Hi Virginia! I go to an alternative doctor. He's intergrative so he works first with alternative and then does convetional if he needs too at last resort. Have you tried a doctor like that. Also are you taking lots of vitamins? How is your thyroid. Conventionals told me mine was fine but when I went back to my alternative he found out it was low and I'm on a natural thyroid medication. Conventionals don't get it somehow with these diseases so I went alternative and he's helping me a lot right now. Lynn --- Virginia Dempsey wrote: > HI Ladies and Gents... > > Yes, weather does effect me. Especially when the > pressure goes down. I have been in horrable pain > the last 3 days and each day that I think it can't > get worse it does. Nothing seems to work, meds, > relaxers, or bio-feedbk. It could be spring but > I really don't know any more... > > Rhonda Huffman wrote: > Hi , yes, for the longest time, the weather > has also affected me too. > Hot/humid to cold/humid cause pain flareups quite > often. I feel like a > human barometer. > > Rhonda Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 17, 2006 Report Share Posted April 17, 2006 Hi Mitzi: Besides arthritis do you also have CFS and Fibromyalgia? If so get to a doctor who's alternative. One who is intergrative is best - they do alternative and use conventional as a last resort. They could also help you a lot with your arthritis. Lynn --- ellemac114@... wrote: > Hi, I'm new here-- just been lurking for a few > days. I'm from central Illinois where we have had > rain, wind, tornados, damp, cold, weather for a few > weeks (seems like forever). My arthritis is killing > me!! My hands are so sore I can hardly use them. > Been taking Aleeve, but it doesn't seem to touch it > in this weather. I have Vicodin which helps the > most, but don't want to get to cozy with it!! I > just need some DRY, WARM, sunshine!! Mitzi Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2006 Report Share Posted April 18, 2006 Hi Lynn, I see a Chiropractor and he helps me out with my alternative ways. The last time I had my thyroid I was told it was fine. I do take tons of vitamins. I am aware that we all have to take vitamins to help us along. The only thing is that I find like my meds that they help for a bit and then they stop. I will be seeing my CFS doctor in NYC on Friday. I really can't wait. I know she will want me to come in more often to coem in for vitamin drips, and if that is what I have to do I will. It just takes a lot out of my to get to NYC. Hubby would take off if I asked to take me but I know it is a busy time for him right now. I appreciate you getting back to me, I will have my doctor do another Thyroid, and have my EBV and HHV-6 cked also. The VA does most of the blood work for me but they dont' do it all. Thanks again, for all your ideas... Ginny lynn paulino wrote: Hi Virginia! I go to an alternative doctor. He's intergrative so he works first with alternative and then does convetional if he needs too at last resort. Have you tried a doctor like that. Also are you taking lots of vitamins? Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2006 Report Share Posted April 18, 2006 -----Original Message----- From: CFAlliance [mailto:CFAlliance ]On Behalf Of lynn paulino How is your thyroid. Conventionals told me mine was fine but when I went back to my alternative he found out it was low and I'm on a natural thyroid medication. Hi Lynn I'd be interested to know what your natural thyroid medication is. Alison God bless Give food to the hungry every day with a simple click, at no cost to you. Visit http://www.thehungersite.com today! Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2006 Report Share Posted April 18, 2006 Hi Alison! I hope you feel better! My natural thyroid medication is called NatureThroid. You could look it up on the web to get info on it. It is helping me. I'm feeling a little stronger. Lynn --- Alison wrote: > > Hi Lynn > > I'd be interested to know what your natural thyroid > medication is. > > Alison > > God bless Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2006 Report Share Posted April 18, 2006 Hi Virginia! Good luck with the doctor and your welcome! Also, if she helps you let me know her name because I live in the next state - New Jersey. My alternative is doing the best he can for me. I do feel a little better. Also, vitimins seem to always help me. He said that CFS and Fibromyalgia is curable in a lot of patients. Lynn --- Virginia Dempsey wrote: > Hi Lynn, > > I see a Chiropractor and he helps me out with my > alternative ways. The last time I had my thyroid I > was told it was fine. I do take tons of > vitamins. I am aware that we all have to take > vitamins to help us along. The only thing is that I > find like my meds that they help for a bit and then > they stop. I will be seeing my CFS doctor in NYC > on Friday. I really can't wait. I know she will > want me to come in more often to coem in for vitamin > drips, and if that is what I have to do I will. It > just takes a lot out of my to get to NYC. Hubby > would take off if I asked to take me but I know it > is a busy time for him right now. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 19, 2006 Report Share Posted April 19, 2006 -----Original Message----- From: CFAlliance [mailto:CFAlliance ]On Behalf Of lynn paulino Hi Alison! I hope you feel better! My natural thyroid medication is called NatureThroid. You could look it up on the web to get info on it. It is helping me. I'm feeling a little stronger. Lynn Thanks Lynn. I've looked it up on the internet and am pleased to see it's available in the UK (where I live) by prescription, if I ever need it! Alison God bless Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 21, 2006 Report Share Posted April 21, 2006 Hi Lynn, Where in Jersey are you?, as I am in Jersey also. small world. Do you belong to NJCFSA? I just got back from the doctor and she will be running a bunch of test. Did get the vit.push as well. Going to try to get in once a month to see her for the drip. We sat down and discussed alot of things that I am experincing. She wants to change a few meds and I will have to see if the VA has them first. I'm hoping that they do. It would help out my pocket book alot. Well, the ride in and back knocked me for a loop so i'm going to rest. Have a great weekend... (((Soft Hugs))) Ginny lynn paulino wrote: Hi Virginia! Good luck with the doctor and your welcome! Also, if she helps you let me know her name because I live in the next state - New Jersey. My alternative is doing the best he can for me. I do feel a little better. Also, vitimins seem to always help me. He said that CFS and Fibromyalgia is curable in a lot of patients. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2006 Report Share Posted April 22, 2006 Hi Virginia! I live in Toms River and I know what you mean when you say you have to rest. I can't work full-time because of this stupid thing so I work part-time in a supermarket. I am covered by benefits because we are unionized. They cut our hours back but it won't last forever so I'll just rest up some. No I don't belong to NJCFSA. What does that stand for. Where in New Jersey do you live? Lynn --- Virginia Dempsey wrote: > Hi Lynn, > > Where in Jersey are you?, as I am in Jersey also. > small world. Do you belong to NJCFSA? I just got > back from the doctor and she will be running a bunch > of test. Did get the vit.push as well. Going to > try to get in once a month to see her for the drip. > We sat down and discussed alot of things that I am > experincing. She wants to change a few meds and I > will have to see if the VA has them first. I'm > hoping that they do. It would help out my pocket > book alot. Well, the ride in and back knocked me > for a loop so i'm going to rest. Have a great > weekend... > > (((Soft Hugs))) > Ginny Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 22, 2006 Report Share Posted April 22, 2006 I take a natural thyroid called Armour thyroid. I have been taking it for 11 years. It has helped me. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 23, 2006 Report Share Posted April 23, 2006 That's great ! Mine seems to be helping too. But yeah I still get sick. Lynn --- wrote: > I take a natural thyroid called Armour thyroid. I > have been taking it > for 11 years. It has helped me. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 24, 2006 Report Share Posted April 24, 2006 Hi Lynn, No I don't work... the CFS and FMS is too bad. i'm in Watchung, I know where Toms River is. It is far for me... Glad you can work part time and have your medical covered..... NJCFSA is New Jersey Chronic Fatigue Syndrome Assoc. I have not belonged for year. Buth they do have conferences in Jersey.... Well need to shut down a bit. I am toally wipped out right now... Have a good day.. Ginny lynn paulino wrote: Hi Virginia! I live in Toms River and I know what you mean when you say you have to rest. I can't work full-time because of this stupid thing so I work part-time in a supermarket. I am covered by benefits because we are unionized. They cut our hours back but it won't last forever so I'll just rest up some. No I don't belong to NJCFSA. What does that stand for. Where in New Jersey do you live? Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 24, 2006 Report Share Posted April 24, 2006 Hi Ginny! NJCFSA - that sounds like something I would like to join. I'm so sorry you can't work. I'm going to see my alternative tomorrow. I was off the past 2 days and am off tomorrow so I'm resting up. It helps somewhat but then as soon as I get in the car and drive up the block I'm pooped again! Are you able to get any medical coverage? Lynn --- Virginia Dempsey wrote: > Hi Lynn, > > No I don't work... the CFS and FMS is too bad. > i'm in Watchung, I know where Toms River is. It is > far for me... Glad you can work part time and have > your medical covered..... NJCFSA is New Jersey > Chronic Fatigue Syndrome Assoc. I have not > belonged for year. Buth they do have conferences in > Jersey.... > Well need to shut down a bit. I am toally wipped > out right now... > > Have a good day.. > > Ginny Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2006 Report Share Posted April 26, 2006 Lynn, Being I was service connected I do get most of my meds thru the VA but if it is not on thier list either I have to do without or spend the $$$. I'ms ure you will like NJCFSA... they all are vol. and suffer with CFS and FMS. There are still some of the original people that I served with. Money is tight right now otherwise I would join again... Enjoy your sunny day... Ginny lynn paulino wrote: Hi Ginny! NJCFSA - that sounds like something I would like to join. I'm so sorry you can't work. I'm going to see my alternative tomorrow. I was off the past 2 days and am off tomorrow so I'm resting up. It helps somewhat but then as soon as I get in the car and drive up the block I'm pooped again! Are you able to get any medical coverage? Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 26, 2006 Report Share Posted April 26, 2006 Hi Ginny! Money is tight for me too. The cut our hours at work. If my boss does it again next week I'm going to talk to her about at least giving me 5 more hours. I'm working 20 1/2 hours this week and I worked 20 last week. The weeks before that were fine. How are you feeling these days. Lynn --- Virginia Dempsey wrote: > Lynn, > Being I was service connected I do get most of my > meds thru the VA but if it is not on thier list > either I have to do without or spend the $$$. > I'ms ure you will like NJCFSA... they all are vol. > and suffer with CFS and FMS. There are still some > of the original people that I served with. Money > is tight right now otherwise I would join again... > > Enjoy your sunny day... > > Ginny Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2006 Report Share Posted April 28, 2006 HI Lynn, What type of work do you do? I don't recall if you told me or not. I have heavy brain fog today. I'm not getting any sleep and that is killing me. I'm sorry to hear that they are cutting yoru hours back. Can you afford that, do you have help? I'm hoping things will turn around for you.... Still waiting for the Va to contact me about the meds. If I don't hear by today, I will call Monday.. You have a good weekend... Ginny lynn paulino wrote: Hi Ginny! Money is tight for me too. The cut our hours at work. If my boss does it again next week I'm going to talk to her about at least giving me 5 more hours. I'm working 20 1/2 hours this week and I worked 20 last week. The weeks before that were fine. How are you feeling these days. Lynn Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 28, 2006 Report Share Posted April 28, 2006 Hi Ginny! My boss gave me my hours back again! Thank goodness. They just do that because of their budget and then it bounces back. I am a cashier at Stop and Shop Supermarket. It's a part time job and I have all benefits including medical, dental, life insurance, pension, etc. I just got a raise. The money isn't all that great but with this illness it's impossible to work full time. My alternative cut my thyroid pill in half for now and told me to stay on the iodine/potassium supplement taking 1 pill 3 times daily. I have to see him on May 24th again. It's monthly visits. He's doing everything in his power to try and help me out. How have you been feeling? Are you ok? Being that you live in New Jersey and you sound really nice if you want my phone # I have no problem giving it to you. Maybe if we talk on the phone it will be comforting for both of us. Also, how old are you? I'll be 57 in August but I look 10 years younger. Take care of your self and you have a nice weekend too. I have off on Sunday and will be resting in bed a good part of the day. And yes, I have someone to talk to at home. My mom lives with me. God Bless and rest up. Lynn --- Virginia Dempsey wrote: > HI Lynn, > What type of work do you do? I don't recall if > you told me or not. I have heavy brain fog today. > I'm not getting any sleep and that is killing me. > I'm sorry to hear that they are cutting yoru hours > back. Can you afford that, do you have help? I'm > hoping things will turn around for you.... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2006 Report Share Posted May 1, 2006 Hi Lynn, That is great news to hear that your boss gave you your hours back....I'm sure that relieves a lot of stress..weall nedour ins and pension....and that is great that you got a raise... Funny you should ask how I am. I had a chrash this weekend. Sat was bad and Sunday was wipe out.. Today I feel a bit better. but I will be resting the rest of the week and seeing may chiropractor and Biofeed back doctor. Hopeing they can help me. If I can drive. I was going to do out and get some food today but I won't get behind the wheel when I feel this way.. We are right around the same age I am 54 and dont' look my age even if I feel ike a hundred 110 today. That would be great to talk give us both someone to talk to who understand what we are going thru. I have my husband and he is great.... Glad you have your Mom to talk to . My mom really doesn't understand the illness nor believes in it... I would rather not post my phone number here. Write me at Combattboots@... and i'll give you the number or you can give it to me.... Stay well my friend... Ginny lynn paulino wrote: Hi Ginny! My boss gave me my hours back again! Thank goodness. They just do that because of their budget and then it bounces back. I am a cashier at Stop and Shop Supermarket. It's a part time job and I have all benefits including medical, dental, life insurance, pension, etc. I just got a raise. The money isn't all that great but with this illness it's impossible to work full time. My alternative cut my thyroid pill in half for now and told me to stay on the iodine/potassium supplement taking 1 pill 3 times daily. I have to see him on May 24th again. It's monthly visits. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted May 1, 2006 Report Share Posted May 1, 2006 Hi Ginny! I crashed yesturday and stayed in bed all day and I'm crashing again now. I have a bad burning sore throat and my body burns from the Fibro. Your mom just dosen't understand. But it's a real illness and boy do we suffer. I would give anything to get better. I will e-mail my number to you personally. Lynn Feel Better --- Virginia Dempsey wrote: > Hi Lynn, > > That is great news to hear that your boss gave you > your hours back....I'm sure that relieves a lot of > stress..weall nedour ins and pension....and that is > great that you got a raise... Quote Link to comment Share on other sites More sharing options...
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