I know that change can be hard but the all new Floxie Hope will have new features and a fresh new look. The new site will have all the exsisint comments, content and posts. Although they will be in a new formart I hope that the new site will bring us together like Floxie Hope has always done.
The new website will have a much needed “facelift” with some new features like podcasts, videos and support groups. However if you would like to still see the orginal homepage click the button below. Also if you have any suggestions or advice for me on the site please reach out.
Be sure to sign up for our email list below to get updates on the new podcast episodes, helpful blog posts, recovery stories and our new online support group by filling out the form below. I hope this new chapter of Floxie Hope will excite you and keep the hope in our community alive.
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Hello Everyone! I hope we will be able to chat again in the comments! Love to all of you!
Happy to receive your comment, Andrea.
I dont know, to be honest. The worst part is, the comments are sorted from the oldest to the newest. Let’s wait some more time as Jason sets everything up, maybe something will appear on the main page, and if not, then ask him where is the best place for the chat.
Thanks Jason. But something’s wrong with comment order on that site and I see comments from 2013 and there’s no button “newest” – only “newer comments”. I’d have to click newer comments like a thousand times to get to 2020. Could you do something about that? Thanks.
Yes I agree totally. Make some sort of arrangements to “QUICKLY” advance through the 26,093 comments to a more recent time.
This may or may not be the right place to be saying this but new floxies should probably get this ebook and read it. https://www.amazon.com/Floxie-Hope-Fluoroquinolone-Antibiotic-Toxicity-ebook/dp/B00VGS34A8/
Guys, I need some support. I probably had some minor tear in my patellar tendon today – I was just walking, not longer than average. It’s now hurtful and red. It’s been 5th month since floxing. I thought the damage is less likely to happen that late. But now I read that some people encounter ruptures even a year after FQ administration. A guy I read article about had his first rupture after 11 months, followed by other ruptures and now is in the wheelchair.
I’m so worried about that. I only took 7 pills of Cipro but with steroid. I did not notice any major improvement in these 5 months. The hair is still falling out in handfulls. I guess my collagen synthesis mechanism is broken. I don’t know what to do. Avoiding activity leads to weak muscles and tendons and it can also cause a rupture indirectly. But the activity is the direct cause of rupture. Will I always have to live in the fear of rupture? To be honest, it’s not life anymore… Not only every step is hurtful but the fear of ruptures in the future makes me want to give up completely… I know there are disabled people and they live but I really don’t want that… And the lack of stability is the worst – I thought I’d be calm at nearly half year out, but the risk of rupture is still very present 🙁
I feel so bad mentally… Please help.
Why my previous comment are now deleted?
Jason…… What are you doing about making it where all the old members can see posts that they exchanged in recent years without the 23,000 plus that appear before them? Fix it!!!!
The font size and color, light gray, very hard to read for Some of us with eye damage . Any chance you can up the font size and use black instead of gray?
There is no,link to the old blog under other resources.
I have made important findings that I know would help Andrea and others but can’t communicate with them.
As you have censored my last post, I just have to comment. Your avitore looked like an angry dominating face. You may want to change that.
Hey John, I don’t have any censors or blocks on the comments. Not sure what you are seeing?
Whew just looked for floxie hope had not popped in for a while could not find it- so glad that it is still up and runing!! It dang near saved my life when I was posioned by levofloxcian almost 300 days ago- I am a lot better now thank you and god bless you best of luck in your new adventure Lisa- more power to the new board and jason! Best to everyone thank you for Flxie hope it really saved me and gave me hope in the dark days when I first got knocked down by the poison RX- thenks for helping!
Jason. I find it impossible to email you or find any way to reach you specifically. Could you please post an email address that actually works? Jason@floxie hope is all over the sites but useless to use or connect with.
Jason. Are you collecting data on vaccines for floxies? Some mitochondrial specialists have fears about the messenger RNA alternatives for our group. I think this is important.
Tell me again how to see the current conversations. ????these are older Feb ones. Yes change is difficult if it’s not clear to people.
Propaganda or fact? Read it and you decide. https://www.bbc.com/news/world-europe-56397157
Magnesium … Seems that plenty of magnesium is one of the very important things for anyone who is floxed. This add came across my Facebook news feed. I am forwarding it because it is the first magnesium supplement that I have found where there is more than one kind of magnesium in it. This has 5 different magnesiums that are claimed to be the most absorbable. John Taylor is recommending that a person use more than one kind of magnesium. This one has 5 different kinds in one capsule. https://autoimmuneinstitute.com/pages/advanced-magnesium
I am posting this in both the “new” and “old ” comments sections because it seems that one must visit several different places to get their information.
Hello out there. Where has everyone gone? Have all the ones who used to post regularly given up on the “New Floxie Hope”? I click on to the site daily and don’t see any of the old gang posting on either the new or the old comments pages.
Have you read about this? https://www.livescience.com/antibody-cocktail-works-preventatively-covid-19.html
Please read this. …. For the many who are having problems navigating the floxiehope web site now. The people’s comments are not in one place any longer. One must visit each of the different subjects (site pages) covered to see the people’s comments about that specific subject. To find that subject and see the comments on it by the people go to the column on the right side of many pages. (header …. “COMMENTS” , there one will find the date and listing of the topic and the name of the person who commented) Clicking on the subjects listed will take you to the web page of the specific subject and you then can read the people’s comments after you have read through the subject. I hope this helps the many who are having problems finding people’s comments and the various subjects and the people’s comments on the various subjects that concern us. I am posting this in both the “old comments section and the new comments section. Good searching.
Just another article on the covid virus. https://www.webmd.com/lung/what-does-covid-do-to-your-lungs?ecd=socpd_fb_nosp_1822_spns_cm5953&fbclid=IwAR0D3gUpLBqMiQ6ZBjbFk5uL1X57mEiXuCyLVwDzX7tIgVgOGMD7BPGBATk#1