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May 18, 2012, 03:37:20 PM
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New28 Story  (Read 7630 times)

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When all else fails, play dead!


Not yet.
The doctor called, apparently a nutritionist will solve my problems??


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I Will Be Diagnosed !


Love to hear what the nutritionist advises especially when on a tight budget.
Hope your having an ok weekend New

 Huge Hug
Sammy


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Any updates New ?
Hope all is well for you sweetie


 Huge Hug


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Sr. Member
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Gender: Female
Posts: 339

When all else fails, play dead!


I have broken a rib! Geesh knows how i did it.

I have a neurotic kitten, she has to be fostered and I'm awaiting the arrival of belly bands for Kaos to stop him scent marking everything in shopping centres, the theory goes he was desexed a bit late so he still has hormones running rampant.


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Broken rib ouchhhhhhh How did you manage that  Question So you haven't been to see the nutritionist New Question
What's wrong with this little kitten ?


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Gender: Female
Posts: 339

When all else fails, play dead!


No idea!
She's had to get over her stress here...She was cleaning the fur off her brother Toby's front leg, and he just let her do it! He's now big enough to stand up for himself.

I have foound a letter in my record from 1990...Hell, that WAS a while ago!


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Hi new 28 karen here again. I read through your four pages and read the recommendations from jay son about the tocapherol injection, i found an article in pubmed about aved ataxia with vitamin e deficiency. the researchers that wrote the articles are sr hammans and cr kennedy. Aved is the name of the condition and is treated with the injections of tocapherol. It is a genetic condition and testing levels of vitamin e in your parents is not a way to definitely diagnose it. You would have to have genetic screening as i am going to do in Rochester New york..It is a recessive genetic condition..Do a google search on the doctors and read some of there research new28.. im sure there probably is research being done somewhere and perhaps you can send your dna to a lab that is researching it..Taking the tocapherol probably wont totally cure you but from what ive read it may prevent further damage and in particular possible blindness as you are possibly at risk for that,,just something for you to consider and mention to your doctor perhaps your doctor can look up the condition for you and start treatment if you are interested. If i understood it correctly the tocapherol helps you overcome the absence of a protein that helps in the assimilation of vitamin e..I found the publication in pubmed a very helpfull website dealing with rare genetic conditions..


 Huge Hug  karen


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Sr. Member
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Gender: Female
Posts: 339

When all else fails, play dead!


Trouble with that theory is I've been through the genetic testing stuff, so have both my parents, my brother, both of my sisters and my daughter. No link has been found.

My brother fainted when they did his, and my youngest sister saw him slide out of his chair and fainted too!!

You've also missed that tocopherol IS vitamin e under a different name is all.


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 Huge Hug HI new, karen again,
i realise that tocapherol is another name for vitamin e. it is my understanding that there are like 8 different forms of vitamin e. I read an article on research done in cows where the were injected with a form of vitamin e a trocapherol i believe it was called..and that with doses of between 2 and 10mg per 100gms of body weight they showed an increase in vitamin e concentration in the serum (blood). i only saw one article about the injection of vitamin e in humans but could not access the article..Pay per view.. I really do believe you need to see another doctor perhaps check with ataxia support forums to see what type of doctor would be appropriate..Ataxia with vitamin e deficiency is listed as an autosomal recessive condition. it does i believe have a recognised genetic marker,, Taking serum levels is not the same as having genotyping done..sometimes conditions occur due to mutation of the genes and in that case family members would not show the gene.. In my case my condition it is autosomal dominant genetic condition passed from generation to generation with a 50/50 chance of getting the gene.

just trying to help a little
karen


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Sr. Member
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Gender: Female
Posts: 339

When all else fails, play dead!


a tocopherol is what I'm injecting now. You probably couldn't find anymore articles because the condition's extremely rare and they haven't done sufficient research yet.
The recognized genetic marker is good. This makes me want to get involved with medical morons again. My own fix is good, but medically recognized would be good too.
Autosomal recessive explains a lot too.


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How's things New  Question haven't heard from you in a long time I do hope things have improved

 Huge Hug
Sammy


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