Sleep disorder symptoms and conditions

HEllo.. I am a 47 year woman, whom started losing alot of hair all of a sudden... I had been losing, a few to 20, throughout a days brushing.> But the last few weeks a good chunk on and off for months.. I started advair last year.. Just got my 3rd refill... I been on albuterol for about 4 years.. My airways close severely..Allergies to foods, chemical, nature flowers and plants.. I also have Apnea sleep disorder which closes airways.. I take, singulair, albuterol, advair, naproxen, and flonase.. daily... I try to take the advair only if really needed.. BUt usually needed every day.. BUT I got the thought the more recent meds have to be the culprit..Not unusual to lose a 100 hairs a day by studies ! But clumps from same spot, all of a sudden! >YEa something not right ! So I started searching..Found so far nsaids such as the naproxen , and this advair both can make you lose your hair and then some ! I also get the itching for your life itch ! HEad to toe ! Dry, Told the doctor I use ever cream, lotion, gel, To Moisturize and it not help..
I been bloating on and off for years, with bowel trouble(IBS).. And nsaids also give constipation problems it seems , as advair has been said by users. BUt the last few years even more so.. I always excerscized..BUt bloat would make me not even appear as I exercise regular.. I have nerve problems all the time.. NEver had blood pressure... ALways read low if anything..NOW I am rating higher blood pressure when I go the dr.. I noticed in the last year My blood vessels show through my skin aLot ! That seemed weird to me ! Perhaps the meds? I been gettin more backaches than usual.. I always have them along in my life..BUT MOre prevailed Now in Lower back . My Eyes stay dry No matter what I do, Even feels like something in my eye, like a small bug or something... BUt never nothing there.. I get the ringing in the ears quite often now.. I think I will quit advair.. As for albuterol I do not know !? I do not know.>BUt Advair is the only meds I started recent.. And the clumps of hair been recent.>So I assume yes the advair !

THe person saying bad mouthing the advair or any med... that it is as prescribed only etc.. YOUR right ! Some people cannot take wat other persons can.> We take meds from a dr.. Not realizing we can have allergy reactions to the med, other people will not have ! PErhaps that it I have another chemical I cannot take in the advair, And perhaps the albuterol !

And another thing.>>The OZone harming chemical had been taken out the ALBUTEROL... they switched it to something else but calls it Albuterol still.. THat is what my Dr told me ! So if harmful to the Ozone, why not harmeful to humans. IT is about Sales to the medical fields more than HElping humans ! Money talks !

GOOD Luck.. and remember GOD is the 1st Physician.>HE cures still !

I to was put on Lipitor 20mg. took it about 1 month and had such pain in my leg muscles I couldn't hardly walk . I went to my doctor he said go off it and I should start Zocor in . A month the pain was worse I couldn't even walk around the mall . I couldn't sleep at night the pain was terrible. Once again I told the doctor he said stop it and we will wait 6 weeks and start Crestor. In six weeks the pain should be gone. It didn't go away I could hardly walk at my job teaching at a Pre School. The pain unreal.I have type 2 diabetes under control for years. Still is.I was told I had arthritis. But now they tell me I have spinal stenosis. I'm on paxil for the depression they said I had and. I feel as bad now as I did 4 years ago when I was on statins. I can hardly walk, my life is pain in my muscles that never leaves and now my back. I was active and watched my weight and walked 3 miles a day. Since taking these meds. I can no longer work, go shopping or go anyplace I have to walk . I have gained a lot of weight . I have something wrong with my knee .I have tried to explain this to 3 doctors and no one listens to me. My health turned for the worse when I started taking Lipitor in 2005. I don't think I'll ever get my life back I am only 58 years old and can't work to support myself.I can't even hold my 1 month old grandson and walk or lift him from his bed. Reading all your messages . I know my health going down like this is from the statin drugs I took . When I sit , I can't walk when I stand Then .I gotta sit in 5 to 10 minutes.And the pain in my knee has progressed. No doctor wants to hear my story and believe me. Thank God I found this web site and read this for my self now I know I'm not crazy. How can I get myself better ? Will I live the rest of my life in pain, and not able to function.Every time I see a doctor they give me another pill to take. I want to just throw them all away .There must to be an answer to this.

Like many of you here... i am extremely happy to have found this website. I have been on Yasmin for about 5 years (frightening!!) and not until yesterday did i realize that all of the peculiar things that have been happening to my body must be connected to this pill. Let's start with the weight gain...

I am 5'9" and have always weighed about 128-132 lbs... As soon as i started taking the pill i jumped up to 138lbs and then over the course of 2-3 years peaked at 160 lbs!! I have struggled to lose that weight for years, exercising daily (with a trainer and also running, doing bikram yoga etc) and eating immaculately (under the supervision of one of New York's best nutritionists..) the result?? not much! i have struggled to lose 10 lbs and have remained at this weight (around 150 ) for about a year!! no matter how many crunches i do, laps i run, and vegetables/ salmon i eat my tummy and midsection is flabby, bloated etc. and i can't shake this weight

next up... i am always tired but yet have trouble sleeping... lie awake at night clutching my chest thinking i'm having a heart attack. fluttering heart/ palpitations etc. they always pass but i thought i was mad until i came across this site.

phantom leg pains... i have inexplicable cramps in my lower legs... thought they were blood clots. have been to see about 20 doctors... all over the world... been tested for blood clots w/ ultrasound, been tested for nerve damage, muscle damage, bone density issues... you name it. even went down the whole eastern medicine, acupuncture route... NOTHING!! nobody can diagnose it or even locate any issue.

these pains also wake me in the night.

last, but not least, i develop hyperpigmentation when i expose my face to the sun... basically looks like a have a moustache b/c my skin darkens... i know this is normal for any birth control/ hormone pill but figured i'd throw it in anyway! also noticed hair on my lip/ sideburns which i promptly removed with laser but i'm now thinking might have been from the Yasmin.

i am midway through a packet but as of today i am stopping. praying that the weight will fall off and the weird aches and pains and imaginary heart attacks will stop.

thank you all for your posts and good luck! does anyone have any updates as to their progress since getting off it??? i promise to post an update in a few months to hopefully help anyone with similar issues!!

all the best!
GM

My hair loss actually started 10 years ago with the advent of menopause. It was less an issue of hair loss but that my hair started to grow in baby fine. With that came a depression. A hormone implant helped. Later, celexa and then lexapro helped particularly with the symptoms of irritable bladder. Other symptoms that started 10 years ago included a slowing pulse rate, lower body temp, lost my eyebrows on the sides, etc. I was bounced between cardiologists and endocrinologists -- blaming a marginally low thyroid. An MD, alternative doctor, blamed mercury which did not abate with two separate rounds of IV chelation. Finally, my heart slowed into the 30s and the exhaustion was extreme. Got a pacemaker which helped but did not cure the exhaustion. Sleep apnea study showed a sleep disorder but no apnea. I am on thyroid meds (125 mg.), mycardis, and .75 patch of estrogen. Wellbutrin 150 mg was added about 6 months ago and that helped tremendously with the tiredness. It was great but I finally noticed that I could see my scalp -- my hair had thinned that much with that low dose. I went to various doctors (including a dermatologist) who never mentioned the connection with any of my meds. They could not tug hair out of my head and suggested a genetic problem (the women in my family have big heads of hair until they die in their 90s). Finally a physician friend in Florida suggested that Wellbutrin might be the problem. I am off of it and tired. Too soon to see if the hair loss is getting better. I just want the loss to stop and to start regrowing my hair. Suggestions? A new doc recommended Provigil for exhaustion but there is some hair loss with that noted on the blogs. I have been taking a b complex, biotin, minerals, a vitamin for hair, zinc, D, MSM -- a handful of supplements. I need something for energy (I am a college professor of graduate students) but will not put my hair at risk. I am lost in all the information about how to stop hair loss and help my hair grow out.

I'm 46, female.. developed blood clots on my lungs for apparently no reason, found them when going to ER and complaining of bad headache, nausea and left shoulder and back pain. I haven't had a recent surgery, nor was on birth control.

I'm dealing with anxiety, depression, unusual headache, horrible back and upper shoulder pain, itching of head, hair falling out during shampooing, , tightness in chest, trouble swallowing, really bad pain in hips, legs and feel like feet swell. I don't sleep well, even on Ambien.. doesn't keep me asleep. I awake in the mornings around 4:30 with diarrhea, nausea, headache and feel awful. Never get a good nights sleep. My hips hurt as well as dealing with parathesias down right arm and into hand.. feels like needles sticking in my hand. Most days I feel wiped out in the afternoon.. as I try and drag myself out of bed to get some excersise.

Does anyone deal with parathesia's down their arms or hands.. what feels like nerve pain?

Has anyone ever tried Aggrenox, also known as Dipyridamole instead?

Or actually tried the real Coumadin, instead of the generic Warfarin?

Has any other woman out there been told not to use a tampon when on her cycle, as this will cause more menstrual bleeding?

I'm so tired of Dr.'s not having personal experience of their own with this drug.. and telling the patient that they are crazy and need to be on anxiety meds or anti-depressants. I just found out that Warfarin is the main ingredient in RAT POISON..

Has anyone EVER gone the totally nutrition route, juiced and gone radical, telling their Dr.'s that they were getting off of all meds?

Does anyone suffer from feeling like their ears are full, or hearing loss?

I'm so tired of feeling afraid.. and tossed around by Dr.'s who really don't want to do the research, nor listen to their patients.

I'd love to hear from anyone who has some insight..on any or all of the questions..

there are some positives with Zyprexa. I took it briefly to treat Schizoaffective disorder, which is half schizophrenia half bipolar disorder.

Zypexa helped me sleep. After years and years of sleep disorder, I actually slept so well and used to wake up feeling invigorated. However, often it would be difficult to get out of bed. Not great if you're trying to work and run your own business.

The downside of Zyprexa is the weight gain. I was always careful about what I ate, but I could not control eating whilst on Zyprexa. I'd literally eat a full meal in the evening and then go out for a pizza afterwards. My weight gain was 30%.

Below is the latest ADR report on Singulair from the United Kingdom. I deleted side effects reports by very small numbers of patients in order to keep the post briefer. This shows the total number of reports since Singulair was approved in the UK.

I don't know the total number of prescriptions for Singulair in the UK. It is considered expensive.

Drug Analysis Print
Drug name: MONTELUKAST
Drug name: MONTELUKAST Report type: Spontaneous
Report run date: 13-May-2008 Report origin: UNITED KINGDOM
Data lock date: 09-May-2008 08:00:02 PM Route of admin: ALL
Period covered: 01-Jul-1963 to 09-May-2008 Reporter type: ALL
Earliest reaction date: 01-Jan-1997 Reaction: ALL

Cardiac disorders-TOTAL 64
Palpitations 29
Myocardial infarction 6
Tachycardia 6
Diarrhoea 84
Dyspepsia 24
Abdominal pain 98
Abdominal pain upper 22
Nausea 84
Vomiting 52
Dry mouth 15
Asthenia 13
Fatigue 45
Malaise 32
Sudden death 1
Pyrexia 10
Chest discomfort 12
Feeling abnormal 16
Influenza like illness 17
Irritability 18
Drug interaction 13
Chest pain 13
Arthralgia 59
Myalgia 38
Muscle spasms 24
Pain in extremity 14
Balance disorder 10
Lethargy 16
Somnolence 23
Psychomotor hyperactivity 25
Headache 221
Dizziness 68
Neuropathy peripheral 7
Convulsion 6
Epilepsy 7
Dysgeusia 7
Hypoaesthesia 6
Tremor 18
Nervous system disorders TOTAL 526
Abnormal behaviour 13
Agitation 12
Anxiety 18
Aggression 30
Depression 23
Insomnia 58
Abnormal dreams 12
Nightmare 49
Hallucination 21
Sleep disorder 15
Psychiatric disorders TOTAL 364
Asthma 36
Allergic granulomatous angiitis 43
Angioedema 12
Swelling face 12
Erythema 13
Pruritus 32
Rash pruritic 17
Rash 55
Urticaria 33

TOTAL NUMBER OF REACTIONS 2841
TOTAL NUMBER OF FATAL ADR REPORTS* 19
TOTAL NUMBER OF ADR REPORTS* 1489

Is this a clue,I have an older son that was born with a birth defect,we live in a city that prides itself on its health care,when i would take him to the mylo clinic,we would see orthopedics, neuron surgery,nutritionists ,neurologists etc everything we needed, now my youngest son,with allergies and asthma,when we would go to clinic also available were behavior specialists and sleep disorder doctors hmmmmm

In Feb 2007 my primary doctor took blood tests and put me on a diet because I was 100 pounds overweight with fatigue symptoms. Blood Tests indicated I had diabetes (126 mg/dl) based on an FPG, and high cholesterol. The FGS was repeated and it dropped to 115 mg/dl. I have been on a low sugar low fat diet since Feb 2007.

In June 2007, I was put on Vytorin (Statin Drug) for Cholesterol. I also saw an Endocrinolist who determined I was a Predibetic and had also Reactive Hypoglycemia based on an OGTT, and determined my fatigue and neuropathy problem was not due to diabetes. She recommended a Rheumatoligist to me in September of 2007.

In late September of 2007. I saw a Rhematolgist for my sleep problems and fatique problems. I had severe muscle fatique (firing pains and numbness), chronic sleep disorder. breathing difficulty during day and when sleeping, difficulty swallowing, vision problems, fluctuations in FBS between hypoglycemia and hyperglycemia symptoms.

He determined after physical examination I had Fibremalagia since all test points on my body were sensitive to touch. He also had his lab do repeat and other blood tests (CPK, Aldolase, etc..), and prescribed a sleep study done by a specialist in my area. He took me off all Caffeine and Vytorin immediately (As I have been off it since that date). He prescibed Diclofenac for Inflamation, Citalopram 40mg for stress and anxiety attacks, Zolpidem 10 mg for Sleeping, and he requested I continue monitoring my blood gluecose twice a day.

After Leaving his office I made an Appointment with the Sleep Study Hospital to have the test done the following week. The study indicated I had Chronic Sleep Disorder where my breathing would stop anywhere from 30 seconds to two minutes during the night. The Sleep Order doctor also indicated that there was something else wrong with me out of his expertise.

In early October 2007, my Rheumatologist contacted me by phone and requested me to leave work and come to his office that afternoon to discuss my blood work. I was scared since they would not discuss it over the phone. The doctor dislosed my blood results and was concerned with a CPK of 2600 (should be less than 155) and my Alolase was six times higher than normal. He suspected I either had Polymyositis (not cureable, but treatable) or Inter-myositis (not cureable or treatable). He said he did not want to start treating me with a medication for it until he knew exactly which one I had. He said the only way to find out was to do a muscle biopsy (about the size of a pencil) on one of my large muscles preferribly a Thigh muscle.

In mid October 2007, I was scheduled to see a general surgeon and a week later I had a minor operation to remove a pencil size piece of my left thigh muscle. It was analyzed by the Childrens Hospital in New Orleans who were experts in the muscular diseases.

In Late October 2007, I was diagnosed with severe myopathy caused by the Statin in the drug Vytorin.

I remain on the same medications, have my blood tested every three months, and the CPK last indicated a reading of 900 (still very high, but it dropped all most 2/3 of what it was six months ago. It can usually take a year or so for most folks my age to fully recover, some do not. I still have the same symptoms, but the firing pains have subsided. My vision had also drastically changed, so I saw an Opthomoligist after providing her all my past records. She indicated I did not have any Renal disfunction which is good.

All the doctors agreed I should continue the stress, sleep, and inflamation medication and none of them have any reported inter-related problems. I am also on an AUTO CPAP machine when I sleep because I have two kinds of Atnea that affects my breathing (muscular and brain related). My breathing patterns seem to change quite a bit and my pressures vary from 7 to 20 and more so on the high side.

I am posting an update on my granddaughterwho has been off for 2 weeks since the story broke in the news. There certainly has been a difference, she's more 'present' when I'm speaking with her, not angry, calmer and she slept through the night the other day when she came over to visit. There were actually no 'scenes' or carrying on. However, in light of the last posting I do not know how she will be affected in the long term, None of us can know that, none of us know how this drug actually works on the brain to create such side effects. I just saw a Singulair commercial on TV and almost got sick. Cody Miller's mom in her post stated that he had no behavioral problems before his death. I imagine that is true for the majority of us. My granddaughter never had the need to go see a counselor before this drug. She was a happy, normal 9-year old. That all changed in only 2 months as her mother took her to a psychologist to find out why she was acting so bizarrely. I am convinced this drug has caused untold misery and should be at least restricted to adults or at most taken off the market. This website is only the beginning at some point those who feel strongly will have to come together and organize against this giant company Merck.

I would also like to point out a table that was in the Swedish study that showed what the adverse drug reactions were. It lists that children had night mares, aggressiveness, sleep disorder, abdominal pain, increased appetite, anxiety, fatique and several others. All of these symptoms are similar to what we are reading on this board.

This study was done in a foreign country before anything was ever announced in the American media. If you take this article to your doctor, please don't forget to print the tables. There is a link on the page.

See this link for the article.
http://www.biomedcentral.com/1472-6904/8/1

Individual case safety reports in children in commonly used drug groups – signal detection
Gertrud Brunlöf , Carina Tukukino and Susanna M Wallerstedt
Department of Clinical Pharmacology and Regional Pharmacovigilance Centre, Sahlgrenska University Hospital, SE-413 45 Göteborg, Sweden
author email corresponding author email
BMC Clinical Pharmacology 2008, 8:1doi:10.1186/1472-6904-8-1

Conclusion
In conclusion, the present study indicates that ADRs are reported for commonly used drugs in children. The number of ICSRs varies in different groups of drugs. A possible signal for montelukast and psychiatric adverse drug reactions was found, which should be further explored.

Table 2
Description of ICSRs for children in the ATC code R03DC. All ICSRs concerned the substance montelukast.

Age (years)
Dose (mg/day)
Treatment duration (when known)
ADR
SPC (Yes/No)

ADR, adverse drug reaction; ICSR, individual case safety report; SPC, summary of product characteristics
Brunlöf et al. BMC Clinical Pharmacology 2008 8:1 doi:10.1186/1472-6904-8-1

I have taken Levaquin 500 mg daily for the last 7 days. I am quitting it today! I am so tired. Cannot sleep! Have severe pain in both of my hips! I do not have a history of sleep disorder or hip pain!!! I even have severe pain in both of my shoulders now as well. My doctors insist this isn't from the med. My pharmacist differs in that opinion!! This stuff is POISON!!!
I am a registered nurse and will preach this to any and everyone who will listen!!!
I only pray I will not suffer a tendon rupture even after I have stopped this med! If that happens I will contact an attorney! Can we get a class-action lawsuit for all of us and to prevent others from this terrible experience???

I took 500 mg each day for three (3) days, terrible nightmares, sleep disorder, and some stomach pain. I have seven days left on the treatment. I hope with everything I've read, I can tolerate it, but it doesn't feel so good on the third day...just listening to my Dr, hope he knows what he prescribed is safe for me.

I've been on topamax for 3 1/2 months & was on 25 mg & then was pushed up to 100 mg when I started to have more severe migraines & "seizing" in my arms & legs. Here are a list of my symptoms: increased sleepiness, gait problems, word recall, more difficulty w/dysgraphia, increased ADD problems, increased lability, increased hypersensitivity to stimuli (seizing in limbs increased), pins & needles, metallic taste in mouth, asthma worsened, sleep became more disrupted, lost weight (already skinny), increased facial hair, strange menstrual symptoms, basilar migraines worsened, hemiplegic migraines started occuring at increased rate, suspicious that it may cause or excacerbate pre-existing sleep apnea (haven't been evaluated yet), feel like a stroke patient, weakness on right side of body, can't drink soda, increased impulsiveness, confusion, increased speech problems, increased GERD...this has really messed me up.

you really should be careful giving this to patients who may have a sleep disorder, previous head injury or breathing issues...Is this safe for people w/ asthma, sleep apnea, cerebral palsy, sleep disorders, etc.? Will these side affects wear off or is permanent?

I have nothing to thank Topamax for.

I am on the levo meds a .175mcg which was reduced from.200 when on the .200 I experience the buning dry eyes also but never considered it to be the med. I also suffer from a fair number of headaches. However the depression i was experiencing for many years has discontinued. Recently and am still going through some sever gastranoial intestaial problems have had ct scans exrays etc they show svere constipation however it is usually the other way i have never been costipated before. Also the sleep disorder, the exact same thing started happening to me about 2 months ago. i have been on this med for 3 years now. It has helped me with the depression but now am considering all these phisycal things to be a result of the med no other explantion.

THETOOLMAN

Been on this medication about 3 months, but take it only at bedtime. I have Periodic Limb Movement and take Mirapex to stop the jerking at night, but have breakthrough movements. This medication was given to help me sleep thru those movements because taking more Mirapex was not a good option. Recent sleep study showed marked improvement. Also take low dose of Neurontin for neck pain. I read that some have tortured nights. That was me before the medication. Before diagnosed with the Periodic Limb Movement, if I took certain cold medicines or caffeine at night, my brain felt like a war zone, I was fitful and agitated, writhing mercilessly in the bed, stuck somewhere between awake and asleep. When taking Sinemet this happened if I wasn't real careful. Now I sleep pretty good for about 5 hours - almost a miracle. If you are a restless sleeper (not a wide awake insomniac) check for underlying sleep disorder before giving up on a pain med that is working for your pain.

I'm a 59 year old male who has sleep apnea among other things. The apnea seems to be getting worse and my sleep disorder physician (pediatric neurologist) prescribed Singular for my allergies as it doesn't have steroids in it. I have taken 4 pills and have had the weird dreams, strange sleep, major muscle aches, cramps in the back and along ribs, head aches and sore throat described by others although it worked great for the first day. I am now feeling the "hyper" and semi-depressed feelings that others have described. Bye Bye Singular!!!!

I'm 44years old.My last shot was the 8 oh may,a week after that i suffer a Mini Stroke (TIA).The doctors believe it was because of the Lupron.No Doctor want to say that for sure.Before the TIA,I have some of the symptems of many of yours like,fatigue, decreased libido, : cholesterol, triglycerides,migraines,disorientation, memory loss ,hot flashes, sleep disorder,lost vision on my Right eye.
After The TIA,this is what I'm suffering at this time.(The most misleading information given is that the TIAs do not do any lasting damage. They do, believe me. I have done a lot of searching, getting info on TIAs and the cause of them. I have kept a graph of when they occur and their severity. Those affecting the right side of the body leave different problems to those affecting the left .TIAs, they are a slow, destructive condition that badly damage the patients confidence in living normally. I never go out on my own now in case of a TIA.
I describes the feeling as like a rippling sensation over the top of her head, this is quickly followed by loss of feeling in either left or right side. Right side tends to affect speech, giving garbled nonsense instead of normal conversation. These TIAs tend to go quickly and do not cause much damage. Left side TIAs cause the weakness in arm and maybe leg as well, but seem to affect co-ordination and awareness. I Don't know what I'm doing, but can speak normally. These TIAs do have more lasting effects, as she can be "vague" for a couple of days before snapping back. .
And all of that Because of Lupron,Can some one help us Please. ******

I just took a prometrium pill tonight for the first time in order to help with my sleep disorder and menopause symptoms. I had visited with an endocrinologist who had prescribed this medication to me along with Synthroid and Vivelle . An hour after taking prometrium I started experiencing severe shortness of breath along with heart palpitations to the point where I thought I was going to have a heart attack ! I am seriuosly thinking of discontinuing all these drugs and allowing nature to continue it's course......seems much safer and comfortable than modern day drugs !

just started taking hz pal 25 mg about 3 weeks ago it works great for me it is a catch all fox my anxeity panic attacks my hives and sleep disorder it works great for me

I fall asleep at night but I cannot stay asleep. I have nightmares and constantly wake up. Than I am exausted during the day. Is this from the synthroid? IF anyone is experiencing this as well, please respond. it is effecting my daily life in such a negative way. I went to a sleep disorder dr. and he wants to do a sleep study on me.

It is currently 3:00 am and for another night I can not sleep.
I am now completing my sixth day of taking Levaquin
On November 7th my doctor prescribed Levaquin (one 500 mg tablet per day for 10 days) for my ear infection. He also prescribed 12 hour Allegra and Allegra D for my allergies. I started having severe sleep disorder early on. Believing that it might be the Allegra, I switched to Equate D (a different decongestant/antihistamine). I still can not sleep. I do not know which drug is messing me up, but one of them certainly is. I realize that antihistamines can cause sleepliness, but in the past, an antihistmine in the morning did not affect my sleep to this extent. Maybe its the additional decongestant. Or, maybe its the Levaquin. I do not know. I do know that for six days I have gotton almost no sleep. To be fair, I have a long history of sleep problems, but never this bad. As an aside, since I started taking Levaquin I have experienced a very unpleasant metallic taste.

hot flashes, sleep disorder, vaginal dryness, bladder/urethra pain, diminishing libido

rectal bleeding which within one week had tba which has lead me to have severe migraines that travel and causes other problems; such as sleep disorder, sleep apnea, seizures, etc. also devloped major gastrological problems. at this current time my digestion is working at only 35%. due to this develop major swelling. have been unable to work for over 18 months and was a healthy 37yr old male to a person who cannot work.f