Thank you!! I know about hematology….what I am looking for is the rarest blood disease.

Anxiety and Panic Attacks

okay i know that the rares sea animal is a dolphin or w/e but other then that dolphin , what is the rarest sea animal ? what is the rarest cat. rarest dog . rarest disease ,rarest fruit , rarest vegitable , if u can answer any1 of those it would be helpful ……rarest pokemon ! lol jkjk but if u can answer any one of these , thank youuuuu

Fat Loss 4 Idiots

The degredation of the mind due to Alzheimer’s disease proves that the mind and, resultantly, the human consciousness are both transient things.

Does this prove that most preconceived notions of an afterlife are fundamentally flawed? Most people believe that we will be able to perceive, evaluate and understand any kind of afterlife that may exist.

But clearly, as Alzheimers proves, the mind cannot possibly survive without a functioning human body. It is a possibility that a kind of eternal soul lives on, but, surely, if the consciousness dies then the thing that makes you an individual, self-aware human will cease also.

Opinions?

Deep Zen Audio Meditation

I need the starter pokemon from the previous pokemon games so if anyone breeds them please trade me one

the pokemon i need are:

squirtle
bulbasaur
chikorita
cyndaquil
totodile
treecko
torchic
mudkip

i do not have any great pokemon to trade in return but i will try my best to meet the requests. i will however infect the pokemon i trade with the rare disease pokerus so you can spread it to you favourite pokemon (for those that do not know what pokerus is, it is a virus that will double the amount of ev’s your pokemon recieves from training. this means your pokemon will become stronger, faster)

my fc: Steve! 4639 6394 4463

Yeast Infection No More

I am 21 and have been diagnosed with Degenerative Disk Disease. I have always been very healthy, and do not smoke, so i believe it is quite rare at my age. I have had pain on and off for over 2 years now, and currently for the last 6 months straight. I used to play basketball, it was my life, and in a way still is, I really just wanna know if I’ll be able to play again. If anyone has had DDD and found a good solution that has worked for them please let me know your story. I have tried all the exercieses, anti-inflam., and chiropractor for months but have yet to find a solution besides injections or surgey which looks to be next on my list. I dont need a total painfree solution, I can play through pain, but it totally locks my core up when i try to do anything. So if anyone has any solutions, or has had the injections or surgey please let me know what happened good or bad. I kno even doctors arent always rt, so i want to get some other opinions from people who have been thru this, thx
Yes I did have electric stem. for 3 months along with the chiropractor and therapy and i also used a lumber trackion all with no results good or bad. The treatment did not start that aggressive with all those things, but we tried to add things and build my strength up but it didnt seem to help at all. I’m getting my mri this week and seeing my orthopedic the next week with results and what he thinks is best to do, I just want to get other peoples opinions and experiences, so that i can develop better questions and ideas to ask my doctor. Thanks a lot for your answers so far, anymore would be greatly appreciated…

Fit Yummy Mummy

I want one that is rare to have, but still easy to talk about.
I said I wanted a rare one. I DO NOT want Eczema.

Anxiety Info

It is very rare, 178 cases in literature since 1930. I’m concerned about life expectancy and if it is hereditary. BUT!, I also want to know what I could possibly be facing. I am seeking treatment with Interferon-Alpha.

Angina and Diet

Disability is non-contagious, rare disease. Meds (Opiate derivative & Interferon) and pain keep me from working, though I could do part-time work seated.

The One-Minute Cure

Are there any statistics kept on the prevelance of Hemiplegic migraine syndrome either familial or sporadic (I am guessing FHM would be easier as it is more throughly researched). I understand it is very rare- it is not even indexed as a rare disease! I cannot find any organisation focused on it or any migraine variant really. I have been having a HM for about a week and a half, at first they thought I had a stroke and then multiple sclerosis but nope nope- just an awful migraine that’s disabled half of my body and put me on a cane! I’ve had them before, to a lesser degree and never thought anything about it… Anyway, any info beyond the basics I’ve already found with google would be helpful

-Nicole

Deep Zen Audio Meditation

And, any info on time it will take for the ravages of Hep-C to make it unbearable to live with it any more. I’m a stage 1, with minimal (level 2) inflamation & I already am disabled (literally) with exhaustion & muscle pain/spasms. I have a history of depression, diabetes & other stuff which makes me a poor candidate for interferon/riboviron treatment. Also, I’m not sure I want to take the risk of blindness,(more likely with diabetics like me) no matter how “uncommon” it is. Notice its not listed as “Rare”. nor do I like the idea of facial or ocularmotor palsey–it doesn’t say that’s temporary or reversable. How long do I have before the discomfort of the disease makes suicide look real good?

The Hidden Secret