[Serious] Multiple Sclerosis Map: my latest web project
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[Serious] Multiple Sclerosis Map: my latest web project
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 RE: Multiple Sclerosis Map: my latest web project
September 21, 2019 at 5:49 pm
(This post was last modified: September 21, 2019 at 5:50 pm by Athene.)
Nice job, Atlas!
Is it a work in progress? I think it would be cool to be able to click on a country and get links to regional resources, if they're available. 
Nice job Atlas! I shared it on my facebook page.
God thinks it's fun to confuse primates. Larsen's God!
 (September 21, 2019 at 5:21 pm)Jackalope Wrote: I dunno, it just seems poor form to critique an MS patient's efforts at outreach. If it makes him feel better, it's helped at one MS patient. What possible harm is there in that? I never said there was any harm in it. If it makes Atlas feel better, if it improves his outlook, all well and good. *shrug* Boru
‘I can’t be having with this.’ - Esmeralda Weatherwax
It would be nice to know the percentage of population having MS. Is it better medical care and early diagnosis or are there regional/ genetic risk factors?
God thinks it's fun to confuse primates. Larsen's God!
 RE: Multiple Sclerosis Map: my latest web project
September 22, 2019 at 2:18 pm
(This post was last modified: September 22, 2019 at 2:53 pm by WinterHold.)
(September 21, 2019 at 4:45 pm)BrianSoddingBoru4 Wrote:(September 21, 2019 at 4:15 pm)Jackalope Wrote: We're talking about it and raising awareness right now, in this thread. MS's name is known, but everything else about the disease is either hard to reach or not quite understood by patients. The moment I got diagnosed, I had no knowledge about the numbers of patients, or where are they located. The doctor gave me the number of a Rebief medicine agent and left me with that. I'm just saying that information are priceless. From the number of patients to how much the disease is affecting on every place. At least I don't feel alone with this map; and if one thing I realized its this: There is a damn epidemic regarding this disease, IDK if it's food or cigarettes or genes. (September 21, 2019 at 5:49 pm)Athene Wrote: Nice job, Atlas! Thank you Athene  Yes; the regional resources are a nice idea, I will see if I can implement it right. I can already add whatever to the country's popup. (September 21, 2019 at 6:06 pm)chimp3 Wrote: Nice job Atlas! I shared it on my facebook page. You're the man; chimp3 ^_^ Thanks for the share (September 21, 2019 at 6:07 pm)BrianSoddingBoru4 Wrote:(September 21, 2019 at 5:21 pm)Jackalope Wrote: I dunno, it just seems poor form to critique an MS patient's efforts at outreach. If it makes him feel better, it's helped at one MS patient. What possible harm is there in that? You know, it feel quite good. Helping with a tiny fraction feels amazing. (September 21, 2019 at 6:20 pm)chimp3 Wrote: It would be nice to know the percentage of population having MS. Is it better medical care and early diagnosis or are there regional/ genetic risk factors? Nobody knows the source of M.S; but there are speculation and theories, genetics are a suspect, so as cigarettes and environmental factors. I will add the percentages; seems like a fine idea. (September 21, 2019 at 6:20 pm)chimp3 Wrote: It would be nice to know the percentage of population having MS. Is it better medical care and early diagnosis or are there regional/ genetic risk factors? I calculated the prevalence in every 100,000 though: new map: http://www.bytsnbytes.com/ms_oracle/ms_oracle_map (September 28, 2019 at 9:26 pm)AtlasS33 Wrote:(September 21, 2019 at 6:20 pm)chimp3 Wrote: It would be nice to know the percentage of population having MS. Is it better medical care and early diagnosis or are there regional/ genetic risk factors? Shared that also! Thanks!
God thinks it's fun to confuse primates. Larsen's God!
(September 28, 2019 at 9:45 pm)chimp3 Wrote:(September 28, 2019 at 9:26 pm)AtlasS33 Wrote: I calculated the prevalence in every 100,000 though: You are mostly welcome, chimp3 Thanks for the share
 (September 28, 2019 at 9:26 pm)AtlasS33 Wrote:(September 21, 2019 at 6:20 pm)chimp3 Wrote: It would be nice to know the percentage of population having MS. Is it better medical care and early diagnosis or are there regional/ genetic risk factors? Some of you numbers on rate/prevalence don't make sense. They are not matching other published rates. For instance, look at England (~population 55 million) and Germany (~population 83 million). You have the total cases in both countries as a little more than 100,000 but rate/100,000 in England as 0.11 and Germany as 81.
Being told you're delusional does not necessarily mean you're mental.
RE: Multiple Sclerosis Map: my latest web project
September 30, 2019 at 3:04 am
(This post was last modified: September 30, 2019 at 3:46 am by WinterHold.)
(September 29, 2019 at 7:41 am)wyzas Wrote:(September 28, 2019 at 9:26 pm)AtlasS33 Wrote: I calculated the prevalence in every 100,000 though: I read your comment yesterday and tried to check the numbers of prevalence. The U.K gave me 1.784553980215224 per 100,000 . I used the following: MS CASES/Total Population X 100000 mmm so I disabled the prevalence for now until I find what's wrong in the code.. Comments like yours, Chimp3 and Athene are very useful for me. If you or anybody else find a mistake in my calculations is would be very useful to notify me about so I try to fix them or suggest ideas for me to implement and make the map better |
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[Serious] Multiple Sclerosis Map: my latest web project
