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Anyone diag.w/mental issues from cfs
by chadry, Oct 17, 2009 07:24AM
My son who is now 29 was diagnosed when he was 17 with CFS. They say he must have had a mild case of mono that went undetected. We probably just thought it was the cold or flu.
He has had his bouts over the years with the fatigue. Sometimes for a few days and sometimes for a few weeks.
About a 1 1/2 he went through some very stressful situations. Loss of his business and a personal betrayal that occurred with this. He was pretty devastated at the time. He felt hopeless because he had worked so hard to get there.
He did not see a way out. He began sleeping again and then he was diagnosed as depressed and put on all kinds of meds. These meds were driving him crazy and he kept telling the doctors this so what do they do they up the dose or add other meds to it. so he went into a hospital and they said he was not depressed he was bi polar.
Now new meds and he looks and feels horrible. I am so worried about him.
He can't work because he hurts all over especially in his hands and knees. The little bit of energy he does have the meds take away.
Has anyone else ever been through this. Can the CFS mimic the signs of bi polar. My son does not feel it is CFS because he says he knows that he gets tired usually only once or twice a year and then he is OK again
I have been doing more research again. It seems there is a lot more info now then when he was younger. I tried to explain that in times of stress his body may be reacting to it a lot different than other peoples.
he has state insurance so his doctor choices are limited. I am at the point where I will pay for a doctor visit so he can get tests done and a really good check up.
I told him that we need to see a new physc. and i will pay for it. We need some new sets of eyes on this. We need to start at the beginning again and not have meds just thrown his way and when they don't work or make him worse adding more or upping the dosage. He does not like living like this but with the insurance he has he is at their mercy. He has agreed that he does need new doctors and I told him not to worry about the money part i will do what i have to to get him to see other people.
There is no spark in his eyes at all. He has always been on the thin side but now he looks horrible. I am so worried.
I do not think it is depression or bi polar. I am thinking back to his childhood and until he got diagnosed with CFS in his senior year he was a very happy healthy child. The reason i took him to be checked is because of the new sleeping pattern. he was never like that growing up.
Any thoughts or suggestions would be greatly appreciated.
Chadry
He has had his bouts over the years with the fatigue. Sometimes for a few days and sometimes for a few weeks.
About a 1 1/2 he went through some very stressful situations. Loss of his business and a personal betrayal that occurred with this. He was pretty devastated at the time. He felt hopeless because he had worked so hard to get there.
He did not see a way out. He began sleeping again and then he was diagnosed as depressed and put on all kinds of meds. These meds were driving him crazy and he kept telling the doctors this so what do they do they up the dose or add other meds to it. so he went into a hospital and they said he was not depressed he was bi polar.
Now new meds and he looks and feels horrible. I am so worried about him.
He can't work because he hurts all over especially in his hands and knees. The little bit of energy he does have the meds take away.
Has anyone else ever been through this. Can the CFS mimic the signs of bi polar. My son does not feel it is CFS because he says he knows that he gets tired usually only once or twice a year and then he is OK again
I have been doing more research again. It seems there is a lot more info now then when he was younger. I tried to explain that in times of stress his body may be reacting to it a lot different than other peoples.
he has state insurance so his doctor choices are limited. I am at the point where I will pay for a doctor visit so he can get tests done and a really good check up.
I told him that we need to see a new physc. and i will pay for it. We need some new sets of eyes on this. We need to start at the beginning again and not have meds just thrown his way and when they don't work or make him worse adding more or upping the dosage. He does not like living like this but with the insurance he has he is at their mercy. He has agreed that he does need new doctors and I told him not to worry about the money part i will do what i have to to get him to see other people.
There is no spark in his eyes at all. He has always been on the thin side but now he looks horrible. I am so worried.
I do not think it is depression or bi polar. I am thinking back to his childhood and until he got diagnosed with CFS in his senior year he was a very happy healthy child. The reason i took him to be checked is because of the new sleeping pattern. he was never like that growing up.
Any thoughts or suggestions would be greatly appreciated.
Chadry
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I hope you will check out MedHelp's fibro/CFS forum and join us and also invite your son. There are groups, such as the CFIDS Association of America and the new Whittemore Peterson Institute who are there for us.
The best thing you can do for your son right now is be supportive. Trust me... he needs all of the support he can get.
To find a physician in your area who regularly diagnoses and treats CFS, google, "Co Cure's Good Doctor List" (read the disclaimer first)
Link to MedHelp's fibro/CFS forum:
http://www.medhelp.org/forums/Fibromyalgia---CFS/show/44?camp=msc&;personal_page_id=495962
chadry