Guest guest Posted November 2, 2000 Report Share Posted November 2, 2000 In a message dated 11/2/00 5:51:04 AM Eastern Standard Time, egroups writes: << Janet, depending on exactly where your pain is, it could be the spleen. >> Janet.It could also be your kidneys or a bad mattress....please make it a point of asking your doctor.it IS important. Joanne Quote Link to comment Share on other sites More sharing options...
Guest guest Posted April 18, 2001 Report Share Posted April 18, 2001 Lee-Anne, My husband has ringing in his ears and sees one of the world specialists in NY, Dr. Abraham Shulman. This is what we have learned. He told me that autoimmune diseases can cause hearing disturbances. I am very sensitive to loud noises. There is no cure, but there are lots of treatments that can help improve the situation. One treatment is steroids, so it may be another medication that is effecting you. here is a site with info about tinnitus (ringing in your ears) http://www.ata.org/about_tinnitus/ You should find a real expert if a medication change doesn't stop the ringing. In a message dated 04/18/2001 3:12:16 AM Eastern Daylight Time, rheumatic writes: I have had trouble off and on, ( definitely "on" right now) with my ears ringing and ringing and RINGING! ( Sorry to shout!) I am convinced this is drug induced and I hope when I can get off the steroids that it corrects itself. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 2, 2001 Report Share Posted June 2, 2001 here's the contact > info to get you started on possibly becoming a claimant in the class-action > lawsuit against vaccine manufacturers: call Bothwell at > 1-866-829-7529 and let her know you are interested. They'll then send you > the intake paperwork and process your situation from there. They'll let you > know what other info they need, as well (i.e. vaccination records, etc.). Unless something has changed, when I called, I was told this was NOT a class action suit, but that they were filing individual cases. Jax FL __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2002 Report Share Posted January 30, 2002 " Remember! We are here to share our personal experience on living positive, quality lives with CMT. " Have you all noticed this lately? I just thought I'd share the info from my latest dr appt today. My disability benefits begin in April and I have not been able to work since September because of pain and extreme fatigue related to CMT. My visit to my family dr was a regular check up and to check on my progress in recovering from a few years of increasing stress mentally and physically at work. In 4 months I have begun to exercise a little on a Bowflex machine, but hesitated to increase this activity because of continuing fatigue. Additionally I do not sleep well most nights because of cramping in my legs and intermittant muscle twitching all over. That has lessened since I've been off work, but still happens 4 out 7 nights a week. So anyway, my doctor has recommended aerobic exercise such as swimming, biking, or rowing. Since it is the dead of winter here in PA, and I already have a rower in the Bowflex, I have decided to try rowing. He recommended increasing a minute a week(or more, if I am able) until I reach 20 minutes rowing in addition to my regular strength maintenance exercises I do now. I have read that some of you were advised not to exercise at all, but to me, my dr's advice seems to make sense. I am going to try it. I think the key is moderation, and exercise in the past has made me feel better--when I was working a few years ago, I would notice better balance and more stamina on the days I did exercise before work. My dr says getting my heart rate up for an extended period of time now will help with increasing stamina, and provide more restful sleep at night... In addition to the anti-inflammatory, the anti-depressant, and the pain medication, and continued psychotherapy. Also I received an article about taking Vitamin E for leg cramps so I am starting that too. In the Summer it will be easier for me since in the past I have enjoyed bike riding and swimming. It's been over a year since I tried to do either one, so I hope I will still be able when summer rolls around. So I will keep you all posted with how it seems to be going. The dr I saw today is my regular PCP Family doctor. Friday I will be seeing my ortho and asking his advice also. I think each of these drs has learned a lot about CMT since having me as a patient. I have asked much from them as far as keeping me functional as long as possible in my career in open heart surgery, and I have done much more with my life than was expected when I was diagnosed in 1976. At 35, I have a lot more living to do, and I will continue to work on helping myself be as " able-bodied " as I can. I don't think it will always be easy, so I am glad I have this site for support and advice! Thank you all Joyce __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted January 30, 2002 Report Share Posted January 30, 2002 --- Joyce S <imjerce@...> wrote: > > " Remember! We are here to share our personal > experience on > living positive, quality lives with CMT. " > Have you all noticed this lately? > > I just thought I'd share the info from my latest dr > appt today. Also I > received an article about taking Vitamin E for leg > cramps so I am starting that too. > Joyce; I have been taking vitamin E since Thanksgiving, Seems to make a small difference in the " Ben Gay " sensations that I have. Sure can't hurt! Jim Nash > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2003 Report Share Posted June 20, 2003 In a message dated 6/19/2003 1:36:58 AM Pacific Daylight Time, writes: > Subject: I need helpful hints about potty training. > > I will be starting to potty train my son in July. I would appreciate any > helpful advice. We will continue my son's home therapy during this time. > My son > is non-verbal, yet he knows about 44 signs. He is 3.2 months and a charming > > little boy. I am very excited about him learning to go like a big boy. Can > > anyone give me an estimate of how long it usually takes? I want to go about > > this quick and fast, basically having him live on the potty. If anyone on > the > list knows of any programs to make this more successful, feel free to e-mail > me > at Scissors0@.... I would love to hear some personal stories of how you > > went about it, even if it wasn't successful the first time around. I would > like to prevent mistakes if possible. Thanks for your input and enjoy your > summer. > > Dawn > > Attached is a potty training protocol that we followed and our son was able to potty training in 3 days. We were very strict about it and followed it in every way. Hope this helps others. Christy Crider Mom to Dylan (3.2 years old with HFA & Hyperlexia) Corona, CA Email: christycrider@... Group Moderator for Inland Empire Autism Group in So. Cal. <A HREF= " autism_inlandempire_socal/ " > autism_inlandempire_socal/</A> Recommended website: Please visit the official Talk About Curing Autism (TACA) website at: <A HREF= " www.talkaboutcuringautism.com " >www.talkaboutcuringautism.org</A> Disclaimer Note: TACA provides general information of interest to the autism community. The information comes from a variety of sources and TACA does not independently verify any of it. The views expressed herein are not necessarily TACA's. TACA provides general information regarding medical research, treatment options, therapies and nutrition to the autism community. The information comes from a variety of sources and TACA does not independently verify any of it. Nothing in this newsletter/publication/email should be construed as medical advice. Always consult your child's doctor regarding his or her individual needs. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2007 Report Share Posted March 31, 2007 Judy, thank you for sharing your story. I'm so sorry for all you've gone through. Glad you're just about completely back on your feet. All the best. Phyllis Re: HIV & HEP C IS PART OF THE PRE-OP> SCREENING>> it is a good thing and no it is not a problem at all - i just was not> made aware that indeed i was screened and that the results were negative. i> dont care that they tested i just was not told that i was tested and what> the results were.>>>> ------------------------------> TV dinner still cooling?> Check out "Tonight's Picks"<http://us.rd./evt=49979/*http://tv./>on TV.>> > Back to top Reply to sender | Reply to group | Reply via web post Messages in this topic (12) 6. Anybody else scheduled for 03/31/07? Posted by: "wendy22499" olson21@... wendy22499 Mon Mar 19, 2007 7:43 pm (PST) DOB for me will be soon. Anybody else scheduled for end of March? Back to top Reply to sender | Reply to group | Reply via web post Messages in this topic (1) 7. HIV and Hep C Screening Posted by: "miamiangel888" miamiangel888@... miamiangel888 Mon Mar 19, 2007 7:43 pm (PST) Has anyone ever had surgery where they DIDN'T run those tests prior? I assumed that was a normal part of the pre-screening process for any surgery, any doctor, anywhere. I and several family members have had various types of surgery with various doctors in various states and it seems to be a normal practice amongst all of them. Back to top Reply to sender | Reply to group | Reply via web post Messages in this topic (1) Recent Activity 20 New Members 14 New PhotosVisit Your Group Quote Link to comment Share on other sites More sharing options...
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