Guest guest Report post Posted June 18, 1999 Hi there My son who is nearly three has COX deficiency (mito complex IV). He often has episodes of shaking, shivering like he is cold - but obviously he is not! Has anyone else with mito experienced this? What is going on? All help/suggestions gratefully received. Yours - . Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 18, 1999 , My daughter, Savannah, is 3 and has Complex I, Encephalomyopathy. Up until Savannah was approximately 2 years old, she also had the shiver-like thing. It was a quick shiver, as if she was cold, and she would usually do it several times a day. Also, she would have short staring spells occasionally. Then from 2 years old until just a couple of months ago, we didn't see her do the shiver thing or the staring spells as much. Well, a couple of months ago, I started to notice when I would rock her to sleep that she would do a jerking/twitching-like thing. About this same time, it would appear the shiver and staring spells had resumed. Last weekend she did all three several times and she was shaky, lethargic and not eating well, so I called her neurologist. The doctor feels she is having seizures and has ordered an EEG, but wants us to consider trying a seizure medicine - even if the EEG comes back normal, as they often can from what I understand. The doctor had told us a while back, that she felt the staring spells were absence (sp?) seizures and the jerky thing was myoclonic jerks. I have only heard a few people describe what appears to be the same shiver-like episode. The motion is quite fast and I noticed it the most when she was sitting up. Savannah was very ataxic and hypotonic, the physical therapist thought that maybe because of the involuntary movements, that the shiver was a result of her trying to " center herself " . Since Savannah is now 3, she has better control and is walking. Her movements aren't as dyskinetic, so I don't feel this reasoning by the PT is as appropriate now. The neurologist does not go along with the theory either. These are the only 2 explanations I've had so far (seizures and " centering herself " ). I hope it helps. Have you asked your son's doctors about this? If so, what do they say? Lipps Mom to 10, Mackenzie 6 and Savannah 3 (Complex I) > Hi there > My son who is nearly three has COX deficiency (mito complex IV). He often > has episodes of shaking, shivering like he is cold - but obviously he is > not! Has anyone else with mito experienced this? What is going on? > All help/suggestions gratefully received. > Yours - . Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 18, 1999 My son also does this. However, he doesn't shake his whole body, only his arms. He is undiagnosed (suspected mito), and had a normal EEG and MRI. We have no idea what is going on with him, sorry I couldn't be of more help! Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 18, 1999 , I am not diagnosed with mito, just suspect that is our problem, but I also do the shivering thing. It is when I get very nervous I do it. One time on this list there was a big discussion and quite a few people said their kids did it too if I remember right. S. Re: HELP > > > >Hi there >My son who is nearly three has COX deficiency (mito complex IV). He often >has episodes of shaking, shivering like he is cold - but obviously he is >not! Has anyone else with mito experienced this? What is going on? >All help/suggestions gratefully received. >Yours - . > > >------------------------------------------------------------------------ >Looking to expand your world? >http://www.onelist.com >ONElist has 170,000 e-mail communities from which to choose! >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 18, 1999 Hi I mentioned the shaking to 's doctor and he did not make any comment about it as if he seemed not to think it was relevant. I didn't know if it was something to do with the mito or not. Now from what you and others in the group have said I think I'll get back in touch with him and see what he says now I have more info. Thanks - R. Mum to (Complex IV) nearly three, and Chloe age four. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 In a message dated 99-06-17 21:53:03 EDT, you write: << Well, a couple of months ago, I started to notice when I would rock her to sleep that she would do a jerking/twitching-like thing. About this same time, it would appear the shiver and staring spells had resumed. Last weekend she did all three several times and she was shaky, lethargic and not eating well, so I called her neurologist. The doctor feels she is having seizures and has ordered an EEG, but wants us to consider trying a seizure medicine - even if the EEG comes back normal, as they often can from what I understand. The doctor had told us a while back, that she felt the staring spells were absence (sp?) seizures and the jerky thing was myoclonic jerks. >> Dear : Our daughter, Amy is nearly 22 years old. You just discribed her infantcy! These seizures changed when she became about 5 years old, then again at 14 years old and at 16. Now, at 22, she has typical Grand Mall seizures, absence (sp?) seizures, and Drop seizures. The myoclonic jurking has disapeared except durring the grand Mall. Our son, Shea had absence seizures from birth and myoclonic episodes starting when he was 9 years old. They were particularly bad when he had any cold or flu. He turned 20 last month and took himself off the seizure meds and Carnitor when he was 18, with no ill affects. He does experence lethergy and flu-like symptoms when he doesnt get approprite sleep, and he has a learning disability, auditory discrimination, but that's about it. Hope this helps, Lynnie Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 In a message dated 99-06-17 21:53:03 EDT, you write: << Well, a couple of months ago, I started to notice when I would rock her to sleep that she would do a jerking/twitching-like thing. About this same time, it would appear the shiver and staring spells had resumed. Last weekend she did all three several times and she was shaky, lethargic and not eating well, so I called her neurologist. The doctor feels she is having seizures and has ordered an EEG, but wants us to consider trying a seizure medicine - even if the EEG comes back normal, as they often can from what I understand. The doctor had told us a while back, that she felt the staring spells were absence (sp?) seizures and the jerky thing was myoclonic jerks. >> Dear : Our daughter, Amy is nearly 22 years old. You just discribed her infantcy! These seizures changed when she became about 5 years old, then again at 14 years old and at 16. Now, at 22, she has typical Grand Mall seizures, absence (sp?) seizures, and Drop seizures. The myoclonic jurking has disapeared except durring the grand Mall. Our son, Shea had absence seizures from birth and myoclonic episodes starting when he was 9 years old. They were particularly bad when he had any cold or flu. He turned 20 last month and took himself off the seizure meds and Carnitor when he was 18, with no ill affects. He does experence lethergy and flu-like symptoms when he doesnt get approprite sleep, and he has a learning disability, auditory discrimination, but that's about it. Hope this helps, Lynnie Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 In a message dated 99-06-17 21:53:03 EDT, you write: << Well, a couple of months ago, I started to notice when I would rock her to sleep that she would do a jerking/twitching-like thing. About this same time, it would appear the shiver and staring spells had resumed. Last weekend she did all three several times and she was shaky, lethargic and not eating well, so I called her neurologist. The doctor feels she is having seizures and has ordered an EEG, but wants us to consider trying a seizure medicine - even if the EEG comes back normal, as they often can from what I understand. The doctor had told us a while back, that she felt the staring spells were absence (sp?) seizures and the jerky thing was myoclonic jerks. >> Dear : Our daughter, Amy is nearly 22 years old. You just discribed her infantcy! These seizures changed when she became about 5 years old, then again at 14 years old and at 16. Now, at 22, she has typical Grand Mall seizures, absence (sp?) seizures, and Drop seizures. The myoclonic jurking has disapeared except durring the grand Mall. Our son, Shea had absence seizures from birth and myoclonic episodes starting when he was 9 years old. They were particularly bad when he had any cold or flu. He turned 20 last month and took himself off the seizure meds and Carnitor when he was 18, with no ill affects. He does experence lethergy and flu-like symptoms when he doesnt get approprite sleep, and he has a learning disability, auditory discrimination, but that's about it. Hope this helps, Lynnie Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 CLayton also has staring spells and shivering spells and Dr. Kelley does think they are seizures although the only thing his 2 eeg's have shown is some abnormal vertex waves but NO seizure activity. He does believe that although they are seizures he doesn nto want to put him on seizure meds yet - as they could actually trigger in his case other type of seizures - BUT is giving us some med to tkae home (cant remember the name) because he believes that he is a very high risk to develop seizures and that his first seizure could be a statis seizure. Love, Sharon mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins (3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial disorder (presumed to be complex I), eosinophilic gastroenteritis, food allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, sensory integration disorder, tremors, etc........., and the world's best smile) Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 Sharon, how do you fix your computer to be able to make an " ending signature thing " and just put it on each time without retyping the whole thing (that is what some of you do, isn't it?) S. Re: HELP >From: SDidinsky@... > >CLayton also has staring spells and shivering spells and Dr. Kelley does >think they are seizures although the only thing his 2 eeg's have shown is >some abnormal vertex waves but NO seizure activity. He does believe that >although they are seizures he doesn nto want to put him on seizure meds yet - >as they could actually trigger in his case other type of seizures - BUT is >giving us some med to tkae home (cant remember the name) because he believes >that he is a very high risk to develop seizures and that his first seizure >could be a statis seizure. > >Love, >Sharon >mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >disorder (presumed to be complex I), eosinophilic gastroenteritis, food >allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >sensory integration disorder, tremors, etc........., and the world's best >smile) > >------------------------------------------------------------------------ >Where do some of the Internet's largest email lists reside? >http://www.onelist.com >At ONElist - the most scalable and reliable service on the Internet. >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 Sharon, how do you fix your computer to be able to make an " ending signature thing " and just put it on each time without retyping the whole thing (that is what some of you do, isn't it?) S. Re: HELP >From: SDidinsky@... > >CLayton also has staring spells and shivering spells and Dr. Kelley does >think they are seizures although the only thing his 2 eeg's have shown is >some abnormal vertex waves but NO seizure activity. He does believe that >although they are seizures he doesn nto want to put him on seizure meds yet - >as they could actually trigger in his case other type of seizures - BUT is >giving us some med to tkae home (cant remember the name) because he believes >that he is a very high risk to develop seizures and that his first seizure >could be a statis seizure. > >Love, >Sharon >mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >disorder (presumed to be complex I), eosinophilic gastroenteritis, food >allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >sensory integration disorder, tremors, etc........., and the world's best >smile) > >------------------------------------------------------------------------ >Where do some of the Internet's largest email lists reside? >http://www.onelist.com >At ONElist - the most scalable and reliable service on the Internet. >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 Sharon, how do you fix your computer to be able to make an " ending signature thing " and just put it on each time without retyping the whole thing (that is what some of you do, isn't it?) S. Re: HELP >From: SDidinsky@... > >CLayton also has staring spells and shivering spells and Dr. Kelley does >think they are seizures although the only thing his 2 eeg's have shown is >some abnormal vertex waves but NO seizure activity. He does believe that >although they are seizures he doesn nto want to put him on seizure meds yet - >as they could actually trigger in his case other type of seizures - BUT is >giving us some med to tkae home (cant remember the name) because he believes >that he is a very high risk to develop seizures and that his first seizure >could be a statis seizure. > >Love, >Sharon >mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >disorder (presumed to be complex I), eosinophilic gastroenteritis, food >allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >sensory integration disorder, tremors, etc........., and the world's best >smile) > >------------------------------------------------------------------------ >Where do some of the Internet's largest email lists reside? >http://www.onelist.com >At ONElist - the most scalable and reliable service on the Internet. >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 Hi , I know you didn't ask me, but if you are using Internet Explorer for your mail program I can help you. If you are using Netscape, I'm sure it's similar. In Outlook Express 5 go to Tools/Options/Signature. There you can put in your signature line. Just type what you want to say in the edit box. You also have a choice of attaching your sig line to all messages or just new ones. If you are using version 4 for your mail it's in a bit different place. I think it's still under Tools/options. No, I take that back, it's under Stationary which I think is on the Tools menu. Under Stationary there should be something about a sig line. You would do the same thing. Hope that helps. ) Sue ( & Jack)-worn out parents to the greatest kids on earth-- Chris-8: Leigh's Disease, MR (mild), hypotonia, non-walker/talker -7: Leigh's Disease, MR (mild), hypotonia, non-walker/talker, trach tube (tracheomalasia), g-tube/fundo Visit us! http://u2.lvcm.com/jscb > Sharon, how do you fix your computer to be able to make an " ending signature > thing " and just put it on each time without retyping the whole thing (that > is what some of you do, isn't it?) S. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 OK Sue let's try this. I'll try signing that way and see if I did it right. S. mother to 4 and genetic grandmother to 8 with a variety of symptoms: AD(H)D, depression,suspected mito AHA!! It worked! Thank you. Re: HELP > > >Hi , > I know you didn't ask me, but if you are using Internet Explorer for >your mail program I can help you. If you are using Netscape, I'm sure it's >similar. In Outlook Express 5 go to Tools/Options/Signature. There you can >put in your signature line. Just type what you want to say in the edit box. >You also have a choice of attaching your sig line to all messages or just >new ones. If you are using version 4 for your mail it's in a bit different >place. I think it's still under Tools/options. No, I take that back, it's >under Stationary which I think is on the Tools menu. Under Stationary there >should be something about a sig line. You would do the same thing. Hope >that helps. ) > >Sue ( & Jack)-worn out parents to the greatest kids on earth-- >Chris-8: Leigh's Disease, MR (mild), hypotonia, non-walker/talker >-7: Leigh's Disease, MR (mild), hypotonia, non-walker/talker, trach >tube (tracheomalasia), g-tube/fundo Visit us! http://u2.lvcm.com/jscb > > >> Sharon, how do you fix your computer to be able to make an " ending >signature >> thing " and just put it on each time without retyping the whole thing (that >> is what some of you do, isn't it?) S. > > > > > >------------------------------------------------------------------------ >ONElist: where real people with real interests get connected. >http://www.onelist.com >Join a new list today! >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 19, 1999 Sharon, Sue helped, thanks! S. Re: HELP >From: SDidinsky@... > >In a message dated 6/19/99 1:38:53 AM Eastern Daylight Time, >joelinda@... writes: > ><< Sharon, how do you fix your computer to be able to make an " ending >signature > thing " and just put it on each time without retyping the whole thing (that > is what some of you do, isn't it?) S. >> > >I just hit a button - the computer guy helped me set it up and I do know how >to change it - BUT how is it done - I DO NOT KNOW. > >Love, >Sharon >mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >disorder (presumed to be complex I), eosinophilic gastroenteritis, food >allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >sensory integration disorder, tremors, etc........., and the world's best >smile) > >------------------------------------------------------------------------ >Make your voice heard! >http://www.onelist.com >Sign up for the ONElist Weekly Survey. Go to homepage for details. >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 20, 1999 I have Microsoft Outlook Express and created the following signature to add to my messages. " Tools: Stationery: Signature " and then added the text. After composing message " Insert: Signature " and you're done. I'm sure that other e-mail software is similar. Amy (mom to the younger, possible mito, developmental delay, microcepaly, bladder reflux to kidney, GI reflux and GI delay in emptying, CVI, and the best smile and giggle) Re: HELP >From: SDidinsky@... > >In a message dated 6/19/99 1:38:53 AM Eastern Daylight Time, >joelinda@... writes: > ><< Sharon, how do you fix your computer to be able to make an " ending >signature > thing " and just put it on each time without retyping the whole thing (that > is what some of you do, isn't it?) S. >> > >I just hit a button - the computer guy helped me set it up and I do know how >to change it - BUT how is it done - I DO NOT KNOW. > >Love, >Sharon >mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >disorder (presumed to be complex I), eosinophilic gastroenteritis, food >allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >sensory integration disorder, tremors, etc........., and the world's best >smile) > >------------------------------------------------------------------------ >Make your voice heard! >http://www.onelist.com >Sign up for the ONElist Weekly Survey. Go to homepage for details. >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 20, 1999 Thank you Amy and I got it worked out. Everyone is so helpful. I wish I could help everyone else as much as you all help me with everything. I mostly wish I had more answers like for and the weight. I hate it when scary things are happening and we feel so helpless. S. Re: HELP > > >>From: SDidinsky@... >> >>In a message dated 6/19/99 1:38:53 AM Eastern Daylight Time, >>joelinda@... writes: >> >><< Sharon, how do you fix your computer to be able to make an " ending >>signature >> thing " and just put it on each time without retyping the whole thing (that >> is what some of you do, isn't it?) S. >> >> >>I just hit a button - the computer guy helped me set it up and I do know >how >>to change it - BUT how is it done - I DO NOT KNOW. >> >>Love, >>Sharon >>mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >>(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >>disorder (presumed to be complex I), eosinophilic gastroenteritis, food >>allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >>sensory integration disorder, tremors, etc........., and the world's best >>smile) >> >>------------------------------------------------------------------------ >>Make your voice heard! >>http://www.onelist.com >>Sign up for the ONElist Weekly Survey. Go to homepage for details. >>------------------------------------------------------------------------ >>Brought to you by www.imdn.org - an on-line support group for those >affected by mitochondrial disease. > > >------------------------------------------------------------------------ >Looking for a new hobby? Want to make a new friend? >http://www.onelist.com >Come join one of 170,000 e-mail communities at ONElist! >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 20, 1999 is still undiagnosoed with a mito dx but she too has the staring and shiver spells, her neurologist has recommended that she take seizure meds. Said they would help her sleep better (which did happen...9-12 hours staright every day-she doesn't take any big naps during the day) and if she slept better she might develop better - which she is making progress but no milestones. She continues to twitch for 30 mins while she falls asleep. Keep us up to date on his eegs and if he does get a seizure. BTW: 's eeg showed no spikes that would be a seizure but she had waves. Her neurologist said he thought she was having them and we didn't recognise them, I don't agree. She still twitches, as I said. Amy (mom to the younger, possible mito, developmental delay, microcepaly, bladder reflux to kidney, GI reflux and GI delay in emptying, CVI, and the best smile and giggle) Re: HELP >From: SDidinsky@... > >CLayton also has staring spells and shivering spells and Dr. Kelley does >think they are seizures although the only thing his 2 eeg's have shown is >some abnormal vertex waves but NO seizure activity. He does believe that >although they are seizures he doesn nto want to put him on seizure meds yet - >as they could actually trigger in his case other type of seizures - BUT is >giving us some med to tkae home (cant remember the name) because he believes >that he is a very high risk to develop seizures and that his first seizure >could be a statis seizure. > >Love, >Sharon >mommy to Jake (6)(ADHD and too smart for his own good) and fraternal twins >(3/30/97) - Cole -(nda and cute as a button) and Clayton (mitochondrial >disorder (presumed to be complex I), eosinophilic gastroenteritis, food >allergies (milk, soy, eggs, wheat), g-tube, Nissen, latex allergy, DD, >sensory integration disorder, tremors, etc........., and the world's best >smile) > >------------------------------------------------------------------------ >Where do some of the Internet's largest email lists reside? >http://www.onelist.com >At ONElist - the most scalable and reliable service on the Internet. >------------------------------------------------------------------------ >Brought to you by www.imdn.org - an on-line support group for those affected by mitochondrial disease. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 20, 1999 Hi Amy, You can check a box that will automatically insert your sig file to all message or to just new ones. That way you don't have to do it manually. Just trying to be helpful. ) Sue ( & Jack)-worn out parents to the greatest kids on earth-- Chris-8: Leigh's Disease, MR (mild), hypotonia, non-walker/talker -7: Leigh's Disease, MR (mild), hypotonia, non-walker/talker, trach tube (tracheomalasia), g-tube/fundo Visit us! http://u2.lvcm.com/jscb > I have Microsoft Outlook Express and created the following signature to add > to my messages. " Tools: Stationery: Signature " and then added the text. > After composing message " Insert: Signature " and you're done. I'm sure that > other e-mail software is similar. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 20, 1999 , You are quite welcome! I do hope you get to feeling better. Sue ( & Jack)-worn out parents to the greatest kids on earth-- Chris-8: Leigh's Disease, MR (mild), hypotonia, non-walker/talker -7: Leigh's Disease, MR (mild), hypotonia, non-walker/talker, trach tube (tracheomalasia), g-tube/fundo Visit us! http://u2.lvcm.com/jscb > OK Sue let's try this. I'll try signing that way and see if I did it right. > > S. mother to 4 and genetic grandmother to 8 with a variety of > symptoms: AD(H)D, depression,suspected mito > > AHA!! It worked! Thank you. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted June 20, 1999 , You are quite welcome! I do hope you get to feeling better. Sue ( & Jack)-worn out parents to the greatest kids on earth-- Chris-8: Leigh's Disease, MR (mild), hypotonia, non-walker/talker -7: Leigh's Disease, MR (mild), hypotonia, non-walker/talker, trach tube (tracheomalasia), g-tube/fundo Visit us! http://u2.lvcm.com/jscb > OK Sue let's try this. I'll try signing that way and see if I did it right. > > S. mother to 4 and genetic grandmother to 8 with a variety of > symptoms: AD(H)D, depression,suspected mito > > AHA!! It worked! Thank you. Quote Share this post Link to post Share on other sites
Guest guest Report post Posted April 22, 2000 Jeanie DON " T go near the baby food, its vile!! I tried that & thought nothing was better than eating that. The first few weeks while your tummy is healing get liquids in .. protein shakes, soups, if you can tolerate it cottage cheese, scrambled eggs (soft) things like that you don't need to be eating that blechy stuff. Hang in there! Lyssa HELP SORRY TO BOTHER YOU ALL BUT AS THE DAY APPROACHES RAPIDLY I MUST SAY IM GOING NUTS OOPS OR WAS I ALLREADY THERE ANYWAY I WENT AND GOT SOME REALLY CUTE SIPPY CUPS AND SPOONS ETC. AND THE DIET THE NUT. GAVE ME SAID TRY BABY FOOD AT FIRST I KNOW PROTEIN IS A MUST SO I WENT AND BOUGHT EVERY KIND OF MEAN BABY FOOD THEY HAD AND I OPENED UP A COUPLE AND PUKED THERE IS NO WAY I CAN EAT THAT PLEASE HELP....also is cream of wheat and wheatena good jeanie(desperate) ------------------------------------------------------------------------ Enter to WIN one of 10 NEW Kenmore Ranges! Only at sears.com http://click./1/2677/7/_/675032/_/956449749/ ------------------------------------------------------------------------ Quote Share this post Link to post Share on other sites
Guest guest Report post Posted April 22, 2000 Protein shakes are a great way to boost your daily protein intake. They mix up with milk or water .. You can buy them at most health food stores .. and places like GNC .. I like Designer Protein brand and Pro Score 100 both in chocolate flavors. They have about 20-24g of protein per shake (you have to read the labels to see which has how much). I know my surgeon recommended the sugar free Instant Carnation breakfast shakes but those have very low protein .. although they do in a pinch. Lyssa Quote Share this post Link to post Share on other sites
Guest guest Report post Posted April 22, 2000 i dont want to sound stupid but never heard of protein shakes and what kind of soups like tomatoe or chicken broth HELP > > > SORRY TO BOTHER YOU ALL BUT AS THE DAY APPROACHES RAPIDLY I MUST SAY IM > GOING NUTS OOPS OR WAS I ALLREADY THERE ANYWAY I WENT AND GOT SOME REALLY > CUTE SIPPY CUPS AND SPOONS ETC. AND THE DIET THE NUT. GAVE ME SAID TRY BABY > FOOD AT FIRST I KNOW PROTEIN IS A MUST SO I WENT AND BOUGHT EVERY KIND OF > MEAN BABY FOOD THEY HAD AND I OPENED UP A COUPLE AND PUKED THERE IS NO WAY I > CAN EAT THAT PLEASE HELP....also is cream of wheat and wheatena good > jeanie(desperate) > > > ------------------------------------------------------------------------ > Enter to WIN one of 10 NEW Kenmore Ranges! > Only at sears.com > http://click./1/2677/7/_/675032/_/956449749/ > ------------------------------------------------------------------------ > > Quote Share this post Link to post Share on other sites
Guest guest Report post Posted April 22, 2000 is the protein shales in place of the 3 ounces of protein i need at a meal so sorry to bother you HELP > > > SORRY TO BOTHER YOU ALL BUT AS THE DAY APPROACHES RAPIDLY I MUST SAY IM > GOING NUTS OOPS OR WAS I ALLREADY THERE ANYWAY I WENT AND GOT SOME REALLY > CUTE SIPPY CUPS AND SPOONS ETC. AND THE DIET THE NUT. GAVE ME SAID TRY BABY > FOOD AT FIRST I KNOW PROTEIN IS A MUST SO I WENT AND BOUGHT EVERY KIND OF > MEAN BABY FOOD THEY HAD AND I OPENED UP A COUPLE AND PUKED THERE IS NO WAY I > CAN EAT THAT PLEASE HELP....also is cream of wheat and wheatena good > jeanie(desperate) > > > ------------------------------------------------------------------------ > Enter to WIN one of 10 NEW Kenmore Ranges! > Only at sears.com > http://click./1/2677/7/_/675032/_/956449749/ > ------------------------------------------------------------------------ > > Quote Share this post Link to post Share on other sites
