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Temodar and pcp

Common Questions and Answers about Temodar and pcp

temodar

Avatar f tn Now the tumor has recurred a third time and they are trying Temodar again. What other treatment options would you consider at this point?
1515784 tn?1387197290 She had a surgical resection near the end of November and is currently in her third week of Proton Therapy and chemo with Temodar. Her tumor was in the right temporal lobe and the remaining tumor they couldn't remove (about 10 percent they said) is on her right insula. Hoping to chat with other people in the same boat as her. What if any side effects did you incur on Proton therapy? Did everyone who had proton therapy to their brain have to be on a steroid? Did anyone NOT lose hair.
Avatar m tn Merck subpoenaed by DoJ over marketing practices; J&J settles World News | August 10, 2011 Phil Taylor Merck subpoenaed by DoJ over marketing practices; J&J settles Merck & Co has been subpoenaed by the US Department of Justice as part of a criminal investigation into marketing practices for three prescription medicines.
Avatar f tn A month ago my husband (41) had a tumor resection of a GBM in the left temporal/frontal lobe. He is still recovering from surgery and has begun cancer treatment (temodar& radiation) a week ago. He has a previous accident injury where he has struggled with neck pain for ten years. He has been on suboxone for probably 7 years now. He is currently taking his suboxone but is not getting any relief for his head pain.
1524669 tn?1291423170 HI, I AM WITH OLIGODENDROGLIOMA,, NOW ON CHEMOTHERAPY-TEMODAR 350MG.
Avatar n tn Anger and frustration, depression, hallucinations and delusions, headache, impaired vision and coordination, increase in women’s sexual appetites, loss of consciousness, memory loss, paranoia, physical violence, sleepiness, and vomiting. Long-term effects: Brain damage, bronchitis, coma, convulsions.
Avatar n tn Hi I also have complex partial seizures which are being controlled w/anti seizure meds. Along w/1000 ml of Keppra I am taking 400 ml of Lamictal. I have a meningioma in the left petrous apex, meckle's cave and clivas... I had gamma knife radiation in 2002 and the tumor went from 2.6 x 2.2 x1.0 cm to 2.0 x 2.0 x .9 presently. The only symptoms I had at the time of diagnosis was left sided facial tingling. I now have epilepsy, trigeminal pain and severe headaches...
1318483 tn?1318347182 I have been to the ER 3 times during this flare and seen my neuro and PCP. No one seems to be able/willing to give me either enough of something or try something different. So, I will just wait out the flare and hope I get as much mobility back that I had before it started. D - Funny...my mom and I were just talking about UCLA and whether I will be my normal or in a flare when I finally get there. It is pretty sad to hope that I am still flaring when the time comes...
1187071 tn?1279369698 I just hope my PCP is able to go home after work and play with her kids and eat her dinner and able to get a good nights sleep with no problems. And I also hope that she feels guilty for putting me thru this since I can't eat, I can't sleep and I can't play with my kids. Im sorry but that is how I feel. It don't matter if the food is soft the movement of my mouth to eat is what hurts. No OTC meds are helping me. I haven't ate all day and I am hurting anyway.
1462810 tn?1327360449 this tiny bit of PCP - did THAT to me...and as I say, I am extremely healthy, and no illicit drug use...so, imagine the effects on weaker, "drug-taking" folks! I have only had one/two "flashbacks" (one was recently, in my dreams, 30 damn years later!) Horrible stuff! I say to you..DO NOT TAKE Illegal Street DRUGS! Period! Please! Never! OK? Get into some Buddhist-type mind therapy, whatever...but I doubt traditional doctors will help. OK? Good Luck...
Avatar f tn How about you tell us what your exposure was,if you had one at all.
Avatar f tn Apparently its in two places, frontal cortex and thallamus and hence surgery was ruled out. She is on 4th week of radiation [6week plan] and plan to start chemo next week. Now she is experiencing headache and nausea. She is not on steroids. Is this normal? are we missing something? What are we to expect in the near future? Any guidance is appreciated.
Avatar n tn Since the diagnosis of Glioblastoma grade 4 in August, my husband has had the tumor removed and completed the round of radiation and chemotherapy - temodar. Recently I have noticed him being very short fused and argumentative. The slightest thing sets him off as if he had been personally attack. I have also noticed depression setting in. I'm assuming this is all part of the treatment and diagnosis.
794236 tn?1238016706 m still able to walk (with a few balance issues here and there). Anyway, I am NOT a doctor, and each person's situation is different, so don't be afraid to get a second or third opinion on your husband's treatment options. If, after consideration, your husband opts for radiotherapy, ask your doctors about doing it concurrent with Temodar (temolozimide). I took that with my last radiotherapy.
1823499 tn?1370090289 Last week had tilt table test- heart is fine yeah Past wed had emg and barely felt a thing, don't know results yet. yesterday I had a scope done and my stimach is super red. She did a few biopsies. She's checkin for H-pylori and celiac. Celiac is incurable auto immune disease and it makes the body not be able to absob vit. Maybe that's why I have b12 defieciency? It alsoo means I'm allergic to gluten and may need to see a nutritionist yo change eatin habits.
Avatar m tn One thing I can tell you is beware of certain chemos, like temodar , it can cause lukemia in people with NF, and radiation is also a no go for people with NF. Good luck.
Avatar f tn In the following text they use regular mm measurements which is easier to understand. 18mm is around 7/10 of an inch. 20 is .79 and inch and 23mm is just under an inch (an inch is 25mm) about the size of a quarter. I am only a layman, but what I glean from the report is that there is increased blood flow to the area that is enhanced - the area of the tumor - and that is concerning them for being a tumor. Sorry I am not much help. I know your husband has had quite a battle.
Avatar f tn I guess I should get copies and take a look. Although my PCP and NL have not said anything directly, I distinctly get the feeling that they believe I am wasting their time. PCP just referred me to a rheumatologist.... Can you just call an office and request copies? Is it a HIPPA violation to have them mailed, would I need to go there in person?
Avatar f tn Some doctors just think they are where the world begins and ends. It sounds like you need a new PCP as well. Maybe someone younger and more empathetic. I don't remember if you said you were going to look for a new PM or not. It sounds like you need a whole new team of doctors. I do understand "taking a break" from the meds to see if you can live without them.
Avatar f tn Saw my PCP yesterday . He saw my initial results for HIV/std being negative and basically said I'm good . He didn't recommend further testing .
1748105 tn?1314473206 So, my neuro is starting me on Gilenya. I go this Thursday for cardiac and opthamalogic testing so they can have baselines to monitor side effects. Since it is an immunosuppressant if you haven't had the chicken pox or the vaccine you have to get the vaccine and then wait a month to start the drug. Well I call my neuro to tell him I've never had the chicken pox or the vaccine. They call back and tell me to get the vaccine from my pcp.
1823499 tn?1370090289 Since beein off work, the pre fainting has gitten better. And I been payin attention to when and how I move my neck. That is what triggers it. Or stanfing too long also. Im almost sure its related and he done blood work and I havent heard no other reasons for this to happen to me?! Someones opinion please.....
1406332 tn?1315962760 I saw my PCP today for lower leg pain (I fainted and fell a month ago and fractured a small part of the fibula), anyway my shin pain hasn't gotten any better. He said it would take awhile. I mentioned to him that I have a neuro appt. on the 31st. He said: 'Are you still having spells?" ....uh, yes, and they're not 'spells', it's EVERY single day! I told him about the weird feeling in my lower legs when I lay down.
Avatar n tn I have a coworker with my same dx (Hashimotos w/goiter) who sees her local PCP (also my PCP) and her labs are only run every 12 months for TSH only. No ultrasound. This is purely anecdotal, but in my case I would definitely choose my Endo over my PCP.
Avatar f tn I'm looking for a good doctor in or around south bend, a primary care physician, I've been living with my issues since March and they are progressive, I've also lived through 2 pcps , I'm at a loss any help appreciated
956292 tn?1334054869 s advice and support while I have been feeling like I have been losing my mide. I am finally going to my PCP tomorrow and seeking other options after a shutdown at my last neuro apointment. Wish me luck..Any advice on tests I should ask him to run to start ruling things out or in? My neuro insists this is all migraine but I feel it is more than that. I am also bringing him my MRI report to reveiw.
Avatar n tn I'm having vibrating sensations in the middle of my upper back and left should blade and down my arm. What could be causing this?
Avatar m tn is Pneumonia associated with early HIV symptoms - 45 days? i could not understand PCP How long the opportunistic infections take...earliest period.