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Brady's Blog


Guide

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Brady's Blog

If you ever wanted to start your own rosacea blog, we have the tools for you to do this. Then you can refer to your blog when posting elsewhere. It is free for members. And you can set your blog to PRIVATE so that only members you invite can view your blog. While my blog is public, so that you can see how a blog works, when setting up your own rosacea blog you simply set it to PRIVATE and only invite who you want to view your blog. 

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The RRDi understands you may want your own private blog and we sponsor your having one which is included in your subscription! These are the steps

Need help?

For More information on how to use blogs use the Invision Community help center: 

Types of Blogs • Introduction to Blogs

Scroll below to read my first comment in my blog. You can reply to my comment if you register an account with a donation. Then scroll to bottom and find the reply button or find the 'quote' button at the bottom of any post to post your comment. 

You can have your own rosacea blog, included with your subscription, compliments of the RRDi. Why not?  Your own rosacea blog. Think about it. Your own rosacea blog. 

FREE!

Scroll below for comments on my blog. 

29 Comments


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  • Root Admin

We have made the MEMBER FORUM totally private now. If one registers with Sign in with Apple, hides behind a cryptic, mysterious DISPLAY NAME and hides their email address using Apple's Hide My Email service when registering, this makes the RRDi member forum the most private rosacea forum on the internet. 

Guests can only view a portion of our website

Registered Active members have full access to the Member Forum

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  • Root Admin

Updates

In February 2022 we sectioned off about three quarters of our website to members only and only allow guests to view a portion of our website. At the end of March we switched to a subscription based website for members only and allow 95%e of our website to members only who subscribe at least $2/month donation ($1/month for three or more months). Guests were allowed to post for free in our guest forum if until the end of June 2022. Now guest cannot post period unless they subscribe. Watch Season 2 Episode 3 that explains all this. 

Since November 2023, due to a generous donation from one of our members, we have opened up the member forum to guests to view and only allow subscriber members to post. 

My current regimen is using Azelaic Acid generic topical regularly, avoid sugar/carbohydate as much as possible, use the ZZ cream on a regular basis (once a week), stopped drinking alcohol, take loads of vitamins/minerals, drink lots of sugar free seltzer, eating high protein/fat, and continue taking carvedilol. 

Why not donate $2 and gain access to our member forum and create your own rosacea blog?

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  • Root Admin

Just an update on my regimen. The vitamin, minerals, supplements and homeopathic treatment the acupuncturist/nutritionist in Rome, GA prescribed for me as mentioned in my post dated November 27, 2023 I have continued and my health has improved. I can list the treatments I am using for overall health if anyone wants to know. I used Azelaic Acid 15% gel for my rosacea. While I still have occasional white heads and rosacea mainly on my cheeks or nose, it is controlled fairly well. When I eat some sugar I notice it flares up again, but once in a while I cheat on my Rosacea Diet for some ice cream or soft serve since that is my weakness or craving. 

The reason I am not posting as much as I have done in the past is that I had a major life change in May 2022 which affected my mental and emotional stability. It has taken a couple of years to recover. One thing that has helped me is going back to work full time. Now I am emotionally and mentally stable. As anyone knows, stress can aggravate rosacea, and now my rosacea is fairly controlled, but, of course, not healed. That is why rosaceans still search on the internet for solutions that may help control their rosacea. I still find it so odd that rosaceans do not want to come together in a non profit organization and engage in their own research and have a positive impact on the medical community by banding together in numbers to influence the pharmaceutical and skin industry. All rosaceans want to do is rant and rave about rosacea in social media rather than do anything unitedly. It is so sad 😞 . For over twenty years the RRDi has tried, and all we have to show for it is one journal edition and a website full of free rosacea data. Not sure if we can keep it going in 2025 unless we get another generous donor who appreciates what the mission of the RRDi is all about. 

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