tag:blogger.com,1999:blog-8341053492760715216.post4272709740906252095..comments2022-04-15T08:11:16.968-07:00Comments on Xyrpta: A New Miracle Drug for Peripheral Neuropathy, IVIGDick Blide, M.D.http://www.blogger.com/profile/15637183924237529178noreply@blogger.comBlogger4125tag:blogger.com,1999:blog-8341053492760715216.post-19656244913566150832022-04-15T08:11:16.968-07:002022-04-15T08:11:16.968-07:00Unfortunately there are a lot of AIDS/Herpes denia...Unfortunately there are a lot of AIDS/Herpes denials on Herbal cures still out there. I did research on them after I was tested HIV/Herpes positive I was so worried am I going to die soon. I continue my search again on herbal remedy for Std, then I found lots of testimony on how Dr Itua Herbal Medicine Cured HIV/Aids, Herpes Virus,Copd,HPV,Cancer, Hepatitis,Shingles, Diabetes,Epilepsy,Infertility, On websites sharing their testimonies, which made much more sense to me. All the authors pronounce Dr Itua As a man with Good Heart, I pick interest in their testimonies and I contact him about my situation then he gave me procedure how it works, I proceed after one week he courier his Herbal Medicine to me and instruct me on how to drink it for two weeks to cure. I receive His Herbal Medicine so I drank it for two weeks as I was told then after 2 days I go for a test I found out I was cured from HIV/Aids & Herpes Virus, I pay homage to him 2 months ago to his country to celebrate with him on his African festival which he told me it usually happens every year. I know there are lots of (HIV)/Aids Herpes Virus denials of Herbal Remedy movement, the same few doctors and they represent a very small fraction of the community. I could have died because I refused Natural Herbs Cures for so long, but luckily, by the grace of God I am alive to tell my story. Contact Info...Whatsapp Number...+2348149277967,Email...drituaherbalcenter@gmail.com<br />AVAhttps://www.blogger.com/profile/02354897028474636987noreply@blogger.comtag:blogger.com,1999:blog-8341053492760715216.post-13922867390640137562011-04-13T17:08:56.950-07:002011-04-13T17:08:56.950-07:00Please be aware that it's not simple to get IV...Please be aware that it's not simple to get IVIG approved. It cost around 10,000 PER DAY and it must be pre-authorized by your insurance company. Also - it's not an injection. It's an IV administration that takes several hours. You need to a) Make sure your Dr. has tested for all of the typical known causes of PN. b) Get an intradermal skin biopsy (it's the only smoking gun test). They count the number of nerves and do a qualitative evaluation c) Auto immunity is often a diagnosis of exclusion. i.e. If they don't find anything else, they call it autoimmune. It's the autoimmune diagnosis that will make you a candidate for IVIG. IVIG is not yet FDA approved for treating PN, so your doctor will have to know how to write it up properly.Unknownhttps://www.blogger.com/profile/13268616501824631592noreply@blogger.comtag:blogger.com,1999:blog-8341053492760715216.post-3644333746297806812010-04-27T22:06:40.168-07:002010-04-27T22:06:40.168-07:00OMG I'm so enthused about your information on ...OMG I'm so enthused about your information on treatments for PN. I have no doctor assessment of my symptoms, but I have been suffering these horrible sensations in my feet and now beginning in my left hand and fingers for about three years. I've taken Cymbalta and Lyrica plus anti-inflammatories with no real results. However, I must admit that when I ran out of Lyrica (only once did I let this happen...I learn quickly), the pain in my feet intensified so that I thought of chopping my feet off...but then again, what would that feel like. I'm crazy with dealing with these weird sensations plus pain in my feet. And now I'm worrying this will happen to my hands. It's like a curse and I don't know what I've done to deserve it. I'm printing this article and taking it to my doctor who prescribes Lyrica for me. I'm praying I can afford these injections and that I will get my regular old feet back again. Thank you for posting this information.<br /><br />Darlene Wells - Odessa, TexasAnonymousnoreply@blogger.comtag:blogger.com,1999:blog-8341053492760715216.post-245878701198651692009-10-26T14:36:16.737-07:002009-10-26T14:36:16.737-07:00Congratulations on finding a cause and treatment! ...Congratulations on finding a cause and treatment! And thanks for posting this -- I'm still looking for the cause of my PN, which has had a similarly slow progression (and maybe also with the step-by-step progression now that I think about it). I know I've had tests for specific Ig antibody levels, but your posting prompted me to search for methods of detecting Gammopathies. I found an interesting article comparing the detection methods that, pending further review, I'll likely take to my neurologist at my next visit. It may not lead anywhere, but as you know, when you have an "idiopathic" PN, just finding a potentially new angle for investigation makes for a good day. I also live in the northwest, and also if I could return to running, I would be so, so pleased. Good luck with your treatments!<br /><br />(The article I found is "Screening Panels for Detection of Monoclonal Gammopathies" in the June 11, 2009 edition of Clinical Chemistry.)Marlinnoreply@blogger.com