I checked the side effects on Walgreens site and didn't see anything like what he is having. His symptoms sound more like MS to me. Has he been checked for that at all? You might want to do a search for MS symptoms and see if that sounds like a possibility. If so, get an appointment with a neurologist and have some test run to check for sure.
Thanks, we just checked the website out and it seems like he may have a few more of the symptoms on the list. he already has an appointment with a neurologist, and is scheduled for an MRI in less than two weeks.
Hi,
How is your husband? There is no single test that is conclusive for multiple sclerosis. It is good that he will be seeing his neurologist soon and that MRI will be done. Other differentials that should be ruled out include inflammation in the blood vessels, multiple strokes, vitamin deficiency, lupus, stress-related disorders and even a brain infection. Take care and do keep us posted.
Hi, thank you so much for your input. My husband is scheduled for his MRI in 2 days and we are both very anxious. He is also scheduled for an EEG in about two weeks, and hopefully we will get some answers. another symptom that he recently noticed was tremors. hopefully we will get some kind of answers soon! I'll keep you all posted. :)
Hi,
How are you? How was the MRI? I hope everything went well. It is normal to be anxious while waiting for the result. Bu hopefully, the answers will be there soon. Hang on and hope to hear from you soon. Take care always. Best regards.
Hi,
we are doing as well as can be expected I suppose. My husband just received a phone call about his results, and the nurse is asking him to return to the hospital monday morning so they can do another MRI with dyes. She said something about a cyst or something of that nature. she was really unclear. is it possible to have a cyst in your brain? or on it? and what exactly will using the dyes do?, not to my husband, but for the MRI...? Thanks so much for your input, Dr. Santos. It really does mean a lot to us that there is someone out there other than the VA nurses and Doctors that don't like to tell us much.
Hi,
A cyst is a closed, saclike structure that contains fluid, gas, or semisolid material. These can occur anywhere in the body. Majority of cysts are benign, but some may produce symptoms because of their size or location. There are different types of cysts in the brain such as arachnoid cyst, pineal cyst, etc. The treatment for a cyst depends upon the cause of the cyst along with its location. MRI with dyes will help visualize and enhance the location and size of the cyst better than that of MRI with no dye. Discuss the results of the MRI with his doctor for proper evaluation. Write down all questions so that you may not miss them during the consultation. If you don't understand, don't be afraid to ask. They are there to help also. Best regards. Take care always.
Thank you so much for your information and advice again. :) We still have not had an appointment with his Doctor to review the results of his first scan. They had a nurse call us to tell us that he had to do another scan. when he went in the MRI tech asked him what the Dr said about his results, and the tech said that he wasn't able to say anything about the results but that my husband should push for answers. WE JUST AREN'T getting any. That's how it always goes with the Army Doctors tho.. Don't ask, Don't tell, just deal. hopefully we will get some answers soon. I will keep you updated as much as possible. he should be hearing the results in just a few days. THANK YOU AGAIN!!
I have found that the only way to get info with some doctors is to be pushy in a nice way. I would have him call today and say that he had such and such test done on such and such day and that he was calling to find out what the results of that test are. If he doesn't get anywhere, have him call again tomorrow. He needs to be nice, yet firm. Eventually, they seems to get tired of you calling all the time and give you the info you are looking for just so you will stop calling them.
Thanks. I mentioned him trying that, but its very hard to talk to anyone at the VA clinics. they are soooo busy and so backed up all the time it seems like nothing gets taken care of for months unless its VERY serious. i told him to just keep on and see what happens, see if he gets any info from them...
Well, he got SOME answers about his second MRI with dyes... They said to him "Well, there's defintely something there that shouldn't be, so we are sending you to a NeuroSurgeon, If you have any questions, just ask him." My husband asked if it was serious. and they replied, "just ask the neurosurgeon." I'm so tired of these Army Doctors!
Is there any way you could go to a non-military facility? Not sure where you live, but I was very impressed with my neurosurgeon and the facility that I had my surgeries at. I would definitely try to get my friends/family to go there if they needed a neurosurgeon.
There is a way, but it's a very expensive way. :) he has a few appointments lined up so hopefully we will be finding things out soon.
Hi,
Thanks for the update. It can really be frustrating if questions are left unanswered. However, it is best that you wait for the appointment with the neurosurgeon so that he or she can explain better because he is in a better position to do so. Hang on and do keep us posted. Best regards.
If you are in the South Carolina, Georgia, Florida area, let me know. I can contact the University system where I had a lot of my testing and both of my surgeries done and see if there are any special programs that would make it affordable for him to be seen there.
That is VERY nice of you, but unfortunately we are located in the indiana/kentucky area. :( Thank you though.
Well, my husband had his Neurosurgery Consultant Appointment today.... It is a tumor ( they didn't say what kind, but they don't believe it is cancerous) It is a tumor... touching his brain stem... They said that he needs surgery and they would be getting ahold of him within a week or so because the surgeon he talked to today said that isn't is area of expertise per say, so he will be reaching out to another surgeon in hopes of helping my husband and preforming the surgery... I was just wondering... how dangerous would that kind of surgery be? working so close to the brain stem. they said that they couldn't cut it out... so what else would they be doing? the tumor has been growing for years now...they also said that it is risky, but wouldn't give us any details at all.
So sorry you guys are having to go through this. It was hard for me to go through brain surgery when I was single. I can only imagine how you are feeling right now. Praying for both of you.
I'm going to send you a message with a link. The page talks a little about craniotomies and different ways they removed brain tumors. I had a craniotomy done but my surgery was more in the temporal area than the stem. Not sure how similar this would be. If you need to vent, have questions, etc., feel free to message me.
Hi,
How are you? Surgery is indeed very risky since the brain stem controls a number of physical functions including breathing, heart rate, muscle movements, and involuntary tasks such as digestion. Any damage to the brain stem can also interfere with the function of the brain stem and spinal cord. This is why a referral to another neurosurgeon is warranted, if surgery is an option. Radiation treatment can also be done to attempt shrinking the tumor. Do keep us posted on the recent surgery appointment. Hang on and if the explanations by your doctors are not clear, request for further clarification to have a better understanding of the situation. This will also ease any anxiety on your part. Take care always.
So my husband had yet another appointment. The surgeon told him that the tumor is wrapped fully around his brain stem... they told him his military career was over, and he has to have surgery as soon as possible. we have to meet with the surgeon Oct. 29th. they gave him three options as to how to do the surgery. one was going through his ear and drilling straight through, where it would knock out his hearing on that side permanently. also, they could go through his throat, but mentioned something about spinal fluid leaking or something? I'm not sure what the risks with these are at all. they also said they could go through the back of his neck and behind his ear, and didn't say anything about risks with that one. Is there any way to tell which procedure would be best?
Hi,
The best procedure would depend on several factors such as your husband's medical history, experience of the surgeon, the type of tumor present, and the evaluation of his doctors. As much as I want to help which way is best, his attending has a greater say on this matter. Ask for clarifications from his doctors if the medical terms are difficult to understand. Be strong and remember that we are here for you.
Hi. I know it's been nearly a month since I've posted anything regarding my husband's condition. we've had a few more appointments and we have a surgery date finally. We found out that his tumor has been growing since he was born. They said it was a tumor of skin like tissue that for some reason formed between his brain and his skull, instead of on the outside of his skull. we got to really look into the MRI and it was terrifying. His tumor is pushing his brain stem to the right and his brain forward.It is about three times the size of his eyeball...his vision and hearing are becoming more and more disturbed, and he's getting debilitating headaches within the last few days. His surgery is scheduled for December 13. less than a month away. I was just wondering if the headaches should be brought to the attention of the surgeon....any input on the recent info or anything would be greatly appreciated. It's very hard for me to grasp hold of everything right now, and its hard to cope . he isn't allowing me to tell anyone including our family. no one knows about his condition but me, and it's hard not having anyone to talk to about it... he's pretty quiet about it...
Hi,
I know how hard it is to be in your position right now. But be strong and have faith. Be there for him and I know there are many emotions you are both feeling right now. The size of the tumor is responsible for the debilitating headaches and other symptoms he is experiencing right now. Inform his attending physician about any symptom he is experiencing for management as well as for updates. The surgery is less than a month away and the anxiety of waiting is sometimes harder. A support group is really important at this time. If he does not like to tell his family about his condition, ask around in the hospital or ask his doctor if there are support groups in the community/hospital. You can always drop me a note if you need somebody. Will be praying for his surgery and complete recovery. Take care.
Well, My husband had his surgery. He is doing so well! it lasted about 12 hours, and they removed 99% of the tumor! I was completely amazed with the outcome, and with how quickly he is healing and recovering. As far as the surgeons can tell, there is no permanent damage. The only things that we are concerned with is his hearing and having no taste. When they went in for surgery they tested his hearing, and couldn't get a response from his nerves in his right ear, and after surgery, they couldn't either. Other than that, He cannot taste anything. that's not something the doctors mentioned at all, and my husband just mentioned it to me today, after being home for 3 days. is that something that is common with brain surgery, or could it be because he has partial temporary paralysis on his right side of his face? the paralysis isn't even noticable really. he just says it feels a little numb. either way, the surgery went well, and we're both very happy. there were very few set backs so far, he had a slight CSF leak from his nose at one point, and the drain had come out partially in his sleep, so it leaked from his back as well, but other than that, he was fine! thanks for all of your support through all of this! it means a lot to me.