Guest guest Posted April 17, 2001 Report Share Posted April 17, 2001 In the past I have suffered from " extreme bruising " (yeah, I'm sure THAT'S the technical term! LoL). Even went to see my MD about it. This was before I started LC. But, my MD told me it was an electrolyte imbalance and gave me a prescription that helped. I am sorry that I cannot recall what it was. He also recommended a specific vitamin/mineral supplement that I took for a while that kept me from bruising so easily. I wish I could remember what the vitamin/mineral supplement was. Drats! LC has impacted my memory :-( -Marlena >From: H1211958@... >Reply-To: Atkins_Support_List >To: Atkins_Support_List >Subject: Vitamins >Date: Mon, 16 Apr 2001 17:23:05 -0700 > >I bought the vitamin C today...is 500 mg a day okay to take? >I could not find the vitamin K. >I will keep looking for it, will it hurt to take it with the C? >I have about 23 bruises in all, seems like anything I touch with my arms >or legs cause one. >Looks like I have been beaten, some of them are painful too. >I hope the C will work fast. >Thanks for telling me that I needed it and not Iron. >Carol H. _________________________________________________________________ Get your FREE download of MSN Explorer at http://explorer.msn.com Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 1, 2003 Report Share Posted July 1, 2003 I still don't have a definite PLS diagnosis, but the neuro who said he thinks that's what I have recommended heavy vitamin dosages, mostly anti-oxidants. I was concerned about the Vitamin E recommendation -- 800 IU 4x a day, or 3200 IU. That's at least 4 times the recommended dose, and I believe it does build up in your body. He also recommended 500 mg. of Vitamin C 4x a day and 50 mcg of selenium, 4x a day. I'm OK with those dosages, but not the Vitamin E. I have been taking 400 mg of Vitamin E and 500 mg of Vit. C for 10 years, plus a multi-vitamin. I added the selenium and lipoic acid. I opted not to start the mega doses until I have at least a second neuro tell me I have PLS. Hopefully I'll get some answers at s Hopkins later this month. Anyone have any suggestions or comments about the mega doses? Edith Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2003 Report Share Posted July 2, 2003 The neurologist I am seeing was at s Hopkins and is now at the University of land. His name is Dr. Reich. The neurosurgeon is at Hopkins, Dr. Long. Would you be kind enough to send me the list of vitamins you take. Send it to me personally at edith@... so we don't clog up the Yahoo site. Thanks. Edith Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2003 Report Share Posted July 2, 2003 The neurologist I am seeing was at s Hopkins and is now at the University of land. His name is Dr. Reich. The neurosurgeon is at Hopkins, Dr. Long. Would you be kind enough to send me the list of vitamins you take. Send it to me personally at edith@... so we don't clog up the Yahoo site. Thanks. Edith Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2003 Report Share Posted July 2, 2003 Edith who is your appointment with? I ran off the tons of vit. I took to Maragakis and he seemed fine with it all. I felt like they really approved of the CoQ10 and NADH. Please ask them what they recommend and if they will use stem cell testing soon. Thanks, Donna > I still don't have a definite PLS diagnosis, but the neuro who said he thinks > that's what I have recommended heavy vitamin dosages, mostly anti- oxidants. I > was concerned about the Vitamin E recommendation -- 800 IU 4x a day, or 3200 > IU. That's at least 4 times the recommended dose, and I believe it does build > up in your body. He also recommended 500 mg. of Vitamin C 4x a day and 50 mcg > of selenium, 4x a day. I'm OK with those dosages, but not the Vitamin E. > > I have been taking 400 mg of Vitamin E and 500 mg of Vit. C for 10 years, > plus a multi-vitamin. I added the selenium and lipoic acid. I opted not to start > the mega doses until I have at least a second neuro tell me I have PLS. > Hopefully I'll get some answers at s Hopkins later this month. > > Anyone have any suggestions or comments about the mega doses? > > Edith > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2003 Report Share Posted July 3, 2003 Edith, For whom is this message intended? Dolores Re: vitamins > The neurologist I am seeing was at s Hopkins and is now at the University > of land. His name is Dr. Reich. The neurosurgeon is at Hopkins, Dr. > Long. > > Would you be kind enough to send me the list of vitamins you take. Send it to > me personally at edith@... so we don't clog up the Yahoo site. > > Thanks. > > Edith > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2003 Report Share Posted July 3, 2003 Sorry...this was for Donna, and she did reply. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2003 Report Share Posted July 3, 2003 Edith I sent you a personal email. Did you get it? Donna > Sorry...this was for Donna, and she did reply. > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 4, 2003 Report Share Posted July 4, 2003 Donna: Yes I did receive your email. Sorry I didn't let you know. That's quite a lot of pills to take. There are so many different approaches to vitamins and I'll continue to check into what might be best for me. Thanks for your help. edith Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 4, 2003 Report Share Posted July 4, 2003 Donna: Yes I did receive your email. Sorry I didn't let you know. That's quite a lot of pills to take. There are so many different approaches to vitamins and I'll continue to check into what might be best for me. Thanks for your help. edith Quote Link to comment Share on other sites More sharing options...
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